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1.

図書

図書
by László Kürti and Barbara Czakó ; [foreword by E.J. Corey] ; [introduction by K.C. Nicolaou]
出版情報: Amsterdam ; Tokyo : Elsevier, c2005  lii, 758 p. ; 28 cm
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Foreword / E.J. CoreyI:
Introduction / K.C. NicolaouII:
Preface / III:
Explanation of the Use of Colors in the Schemes and Text / IV:
List of Abbreviations / V:
List of Named Organic Reactions / VI:
Named Organic Reactions in Alphabetical Order / VII:
Appendix: Listing of the Named Reactions by Synthetic Type and by their Utility / VIII:
Brief explanation of the organization of this section / 8.1:
List of named reactions in chronological order of their discovery / 8.2:
Reaction categories - Categorization of named reactions in tabular format / 8.3:
Affected functional groups - Listing of transformations in tabular format / 8.4:
Preparation of functional groups - Listing of transformations in tabular format / 8.5:
References / IX:
Index / X:
Foreword / E.J. CoreyI:
Introduction / K.C. NicolaouII:
Preface / III:
2.

図書

図書
Laura Frost, Todd Deal, Karen C. Timberlake
出版情報: Upper Saddle River, NJ : Prentice Hall, c2011  xvi, 475 p. ; 28 cm
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3.

図書

図書
Caroline Cooper
出版情報: Boca Raton, Fla. : CRC Press, Taylor & Francis Group, c2011  xv, 268 p. ; 26 cm
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4.

図書

図書
Michael B. Smith, Jerry March
出版情報: Hoboken, N.J. : John Wiley & Sons, c2007  xx, 2357 p. ; 25 cm
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Preface
Biographical Note
Abbreviations
Localized Chemical Bonding / Part 1:
Delocalized Chemical Bonding / Chapter 2:
Bonding Weaker than Covalent / Chapter 3:
Stereochemistry / Chapter 4:
Carbocations, Carbanions, Free Radicals, Carbenes, and Nitrenes / Chapter 5:
Mechanisms and Methods of Determining Them / Chapter 6:
Irradiation Processes in Organic Chemistry / Chapter 7:
Acids and Bases / Chapter 8:
Effects of Structure on Reactivity / Chapter 9:
Aliphatic Substitution: Nucleophilic and Organometallic / Part 2:
Aromatic Substituion, Electrophilic / Chapter 11:
Aliphatic, Alkenyl, and Alkynyl Substitution, Electrophilic and Organometallic / Chapter 12:
Aromatic Substitution, Nucleophilic and Organometallic / Chapter 13:
Substitution Reactions: Free Radicals / Chapter 14:
Addition to Carbon-Carbon Multiple Bonds / Chapter 15:
Addition to Carbon-Hetero Multiple Bonds / Chapter 16:
Eliminations / Chapter 17:
Rearrangements / Chapter 18:
Oxidations and Reductions / Chapter 19:
The Literature of Organic Chemistry / Appendix A:
Classification of Reactions by Type of Compound Synthesized / Appendix B:
Indexes
Author Index
Subject Index
Preface
Biographical Note
Abbreviations
5.

図書

図書
edited by Bernd Plietker
出版情報: Weinheim : Wiley-VCH, c2008  xv, 279 p. ; 25 cm
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Preface
List of Contributors
Iron Complexes in Organic Chemistry / Ingmar Bauer ; Hans-Joachim Knolker1:
Introduction / 1.1:
General Aspects of Iron Complex Chemistry / 1.2:
Electronic Configuration, Oxidation States, Structures / 1.2.1:
Fundamental Reactions / 1.2.2:
Organoiron Complexes and Their Applications / 1.3:
Binary Carbonyl-Iron Complexes / 1.3.1:
Alkene-Iron Complexes / 1.3.2:
Allyl- and Trimethylenemethane-Iron Complexes / 1.3.3:
Acyl- and Carbene-Iron Complexes / 1.3.4:
Diene-Iron Complexes / 1.3.5:
Ferrocenes / 1.3.6:
Arene-Iron Complexes / 1.3.7:
Catalysis Using Iron Complexes / 1.4:
Iron Complexes as Substrates and/or Products in Catalytic Reactions / 1.4.1:
Iron Complexes as Ligands for Other Transition Metal Catalysts / 1.4.2:
Iron Complexes as Catalytically Active Species / 1.4.3:
References
Iron Catalysis in Biological and Biomimetic Reactions / 2:
Non-heme Iron Catalysts in Biological and Biomimetic Transformations / Jens Muller2.1:
Introduction: Iron in Biological Processes / 2.1.1:
Non-heme Iron Proteins / 2.1.2:
Mononuclear Iron Sites / 2.1.2.1:
Dinuclear Iron Sites / 2.1.2.2:
Summary / 2.1.3:
Organic Reactions Catalyzed by Heme Proteins / Martin Broring2.2:
Classification and General Reactivity Schemes of Heme Proteins Used in Organic Synthesis / 2.2.1:
Organic Reactions Catalyzed by Cytochromes P450 / 2.2.2:
Organic Reactions Catalyzed by Heme Peroxidases / 2.2.3:
Dehydrogenations ("Peroxidase Reactivity") / 2.2.3.1:
Sulfoxidations ("Peroxygenase Reactivity") / 2.2.3.2:
Peroxide Disproportionation ("Catalase Reactivity") / 2.2.3.3:
Halogenation ("Haloperoxidase Reactivity") / 2.2.3.4:
Epoxidations ("Monoxygenase Activity") / 2.2.3.5:
Iron-catalyzed Oxidation Reactions / 3:
Oxidations of C-H and C=C Bonds / Agathe Christine Mayer ; Carsten Bolm3.1:
Gif Chemistry / 3.1.1:
Alkene Epoxidation / 3.1.2:
Alkene Dihydroxylation / 3.1.3:
The Kharasch Reaction and Related Reactions / 3.1.4:
Aziridination and Diamination / 3.1.5:
Oxidative Allylic Oxygenation and Amination / Sabine Laschat ; Volker Rabe ; Angelika Baro3.2:
Iron-catalyzed Allylic Oxidations / 3.2.1:
Simple Iron Salts / 3.2.2.1:
Fe(III) Complexes with Bidentate Ligands / 3.2.2.2:
Fe[superscript 3+]/Fe[superscript 2+] Porphyrin and Phthalocyanine Complexes / 3.2.2.3:
Iron(III) Salen Complexes / 3.2.2.4:
Non-heme Iron Complexes with Tetra- and Pentadentate Ligands / 3.2.2.5:
Oxidative Allylic Aminations / 3.2.3:
Conclusion / 3.2.4:
Oxidation of Heteroatoms (N and S) / Olga Garcia Mancheno3.3:
Oxidation of Nitrogen Compounds / 3.3.1:
Oxidation of Hydroxylamines to Nitroso Compounds / 3.3.1.1:
Oxidation of Arylamines / 3.3.1.2:
Other N-Oxidations / 3.3.1.3:
Oxidation of Sulfur Compounds / 3.3.2:
Oxidation of Thiols to Disulfides / 3.3.2.1:
Oxidation of Sulfides / 3.3.2.2:
Oxidative Imination of Sulfur Compounds / 3.3.2.3:
Reduction of Unsaturated Compounds with Homogeneous Iron Catalysts / Stephan Enthaler ; Kathrin Junge ; Matthias Beller4:
Hydrogenation of Carbonyl Compounds / 4.1:
Hydrogenation of Carbon-Carbon Double Bonds / 4.3:
Hydrogenation of Imines and Similar Compounds / 4.4:
Catalytic Hydrosilylations / 4.5:
Iron-catalyzed Cross-coupling Reactions / Andreas Leitner4.6:
Cross-coupling Reactions of Alkenyl Electrophiles / 5.1:
Cross-coupling Reactions of Aryl Electrophiles / 5.3:
Cross-coupling Reactions of Alkyl Electrophiles / 5.4:
Cross-coupling Reactions of Acyl Electrophiles / 5.5:
Iron-catalyzed Carbometallation Reactions / 5.6:
Iron-catalyzed Aromatic Substitutions / Jette Kischel ; Kristin Mertins ; Irina Jovel ; Alexander Zapf5.7:
General Aspects / 6.1:
Electrophilic Aromatic Substitutions / 6.2:
Halogenation Reactions / 6.2.1:
Nitration Reactions / 6.2.2:
Sulfonylation Reactions / 6.2.3:
Friedel-Crafts Acylations / 6.2.4:
Friedel-Crafts Alkylations / 6.2.5:
Alkylation with Alcohols, Ethers and Esters / 6.2.5.1:
Alkylation with Alkenes / 6.2.5.2:
Nucleophilic Aromatic Substitutions / 6.3:
Iron-catalyzed Substitution Reactions / Bernd Plietker7:
Iron-catalyzed Nucleophilic Substitutions / 7.1:
Nucleophilic Substitutions of Non-activated C-X Bonds / 7.2.1:
Nucleophilic Substitutions Using Lewis Acidic Fe Catalysts / 7.2.1.1:
Substitutions Catalyzed by Ferrate Complexes / 7.2.1.3:
Nucleophilic Substitution of Allylic and Propargylic C-X Bonds / 7.2.2:
Reactions Catalyzed by Lewis Acidic Fe Salts / 7.2.2.1:
Nucleophilic Substitutions Involving Ferrates / 7.2.2.2:
Addition and Conjugate Addition Reactions to Carbonyl Compounds / Jens Christoffers ; Herbert Frey ; Anna Rosiak7.3:
Additions to Aldehydes and Ketones / 8.1:
Oxygen Nucleophiles / 8.2.1:
Carbon Nucleophiles / 8.2.2:
Additions to Imines and Iminium Ions / 8.3:
Additions to Carboxylic Acids and Their Derivatives / 8.4:
Conjugate Addition to [alpha],[beta]-Unsaturated Carbonyl Compounds / 8.4.1:
Michael Reactions / 8.5.1:
Vinylogous Michael Reactions / 8.5.1.2:
Asymmetric Michael Reactions / 8.5.1.3:
Michael Reactions in Ionic Liquids and Heterogeneous Catalysis / 8.5.1.4:
Nitrogen Nucleophiles / 8.5.2:
Synthesis of Heterocycles / 8.6:
Pyridine and Quinoline Derivatives / 8.6.1:
Pyrimidine and Pyrazine Derivatives / 8.6.2:
Benzo- and Dibenzopyrans / 8.6.3:
Iron-catalyzed Cycloadditions and Ring Expansion Reactions / Gerhard Hilt ; Judith Janikowski9:
Cycloisomerization and Alder-Ene Reaction / 9.1:
[2+1]-Cycloadditions / 9.3:
Iron-catalyzed Aziridine Formation / 9.3.1:
Iron-catalyzed Epoxide Formation / 9.3.2:
Iron-catalyzed Cyclopropane Formation / 9.3.3:
[2+2]-Cycloaddition / 9.4:
[4+1]-Cycloadditions / 9.5:
[4+2]-Cycloadditions / 9.6:
Diels-Alder Reactions with Normal Electron Demand / 9.6.1:
Diels-Alder Reactions with Neutral Electron Demand / 9.6.2:
Diels-Alder Reactions with Inverse Electron Demand / 9.6.3:
Cyclotrimerization / 9.7:
[3+2]-Cycloadditions / 9.8:
[3+3]-Cycloadditions / 9.9:
Ring Expansion Reactions / 9.10:
Index / 9.11:
Preface
List of Contributors
Iron Complexes in Organic Chemistry / Ingmar Bauer ; Hans-Joachim Knolker1:
6.

図書

図書
Francis A. Carey and Richard J. Sundberg
出版情報: New York : Kluwer Academic/Plenum Publishers, c2000  xii, 823 p. ; 26 cm
シリーズ名: Advanced organic chemistry / Francis A. Carey and Richard J. Sundberg ; pt. A
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Chemical Bonding and Structure / Chapter 1.:
Valence Bond Description of Chemical Bonding / 1.1.:
Orbital Hybridization / 1.1.1.:
Resonance / 1.1.2.:
Bond Energy, Polarity, and Polarizability / 1.2.:
Bond Energies / 1.2.1.:
Electronegativity and Polarity / 1.2.2.:
Polarizability--Hardness and Softness / 1.2.3.:
Molecular Orbital Theory and Methods / 1.3.:
Huckel Molecular Orbital Theory / 1.4.:
Qualitative Application of Molecular Orbital Theory / 1.5.:
Application of Molecular Orbital Theory to Reactivity / 1.6.:
Interactions between [sigma] and [pi] Systems--Hyperconjugation / 1.7.:
Other Quantitative Descriptions of Molecular Structure / 1.8.:
Atoms in Molecules / 1.8.1.:
Electron Density Functionals / 1.8.2.:
Modern Valence Bond Approaches / 1.8.3.:
General References
Problems
Principles of Stereochemistry / Chapter 2.:
Enantiomeric Relationships / 2.1.:
Diastereomeric Relationships / 2.2.:
Stereochemistry of Reactions / 2.3.:
Prochiral Relationships / 2.4.:
Conformational, Steric, and Stereoelectronic Effects / Chapter 3.:
Strain and Molecular Mechanics / 3.1.:
Conformations of Acyclic Molecules / 3.2.:
Conformations of Cyclohexane Derivatives / 3.3.:
Carbocyclic Rings Other Than Six-Membered / 3.4.:
The Effect of Heteroatoms on Conformational Equilibria / 3.5.:
The Anomeric Effect / 3.6.:
Conformational Effects on Reactivity / 3.7.:
Angle Strain and Its Effect on Reactivity / 3.8.:
Relationships between Ring Size and Rate of Cyclization / 3.9.:
Torsional and Stereoelectronic Effects on Reactivity / 3.10.:
Study and Description of Organic Reaction Mechanismns / Chapter 4.:
Thermodynamic Data / 4.1.:
Kinetic Data / 4.2.:
Substituent Effects and Linear Free-Energy Relationships / 4.3.:
Basic Mechanistic Concepts: Kinetic versus Thermodynamic Control, Hammond's Postulate, the Curtin-Hammett Principle / 4.4.:
Kinetic versus Thermodynamic Control / 4.4.1.:
Hammond's Postulate / 4.4.2.:
The Curtin-Hammett Principle / 4.4.3.:
Isotope Effects / 4.5.:
Isotopes in Labeling Experiments / 4.6.:
Characterization of Reaction Intermediates / 4.7.:
Catalysis by Bronsted Acids and Bases / 4.8.:
Lewis Acid Catalysis / 4.9.:
Solvent Effects / 4.10.:
Substituent Effects in the Gas Phase / 4.11.:
Stereochemistry / 4.12.:
Conclusion / 4.13.:
Nucleophilic Substitution / Chapter 5.:
The Limiting Cases--Substitution by the Ionization (S[subscript N]1) Mechanism / 5.1.:
The Limiting Cases--Substitution by the Direct Displacement (S[subscript N]2) Mechanism / 5.2.:
Detailed Mechanistic Description and Borderline Mechanisms / 5.3.:
Carbocations / 5.4.:
Nucleophilicity and Solvent Effects / 5.5.:
Leaving-Group Effects / 5.6.:
Steric and Strain Effects on Substitution and Ionization Rates / 5.7.:
Effects of Conjugation on Reactivity / 5.8.:
Stereochemistry of Nucleophilic Substitution / 5.9.:
Neighboring-Group Participation / 5.10.:
Mechanism of Rearrangements of Carbocations / 5.11.:
The Norbornyl Cation and Other Nonclassical Carbocations / 5.12.:
Polar Addition and Elimination Reactions / Chapter 6.:
Addition of Hydrogen Halides to Alkenes / 6.1.:
Acid-Catalyzed Hydration and Related Addition Reactions / 6.2.:
Addition of Halogens / 6.3.:
Electrophilic Additions Involving Metal Ions / 6.4.:
Additions to Alkynes and Allenes / 6.5.:
The E2, E1, and E1cb Mechanisms / 6.6.:
Regiochemistry of Elimination Reactions / 6.7.:
Stereochemistry of E2 Elimination Reactions / 6.8.:
Dehydration of Alcohols / 6.9.:
Eliminations Not Involving C--H Bonds / 6.10.:
Carbanions and Other Nucleophilic Carbon Species / Chapter 7.:
Acidity of Hydrocarbons / 7.1.:
Carbanions Stabilized by Functional Groups / 7.2.:
Enols and Enamines / 7.3.:
Carbanions as Nucleophiles in S[subscript N]2 Reactions / 7.4.:
Reactions of Carbonyl Compounds / Chapter 8.:
Hydration and Addition of Alcohols to Aldehydes and Ketones / 8.1.:
Addition-Elimination Reactions of Ketones and Aldehydes / 8.2.:
Addition of Carbon Nucleophiles to Carbonyl Groups / 8.3.:
Reactivity of Carbonyl Compounds toward Addition / 8.4.:
Ester Hydrolysis / 8.5.:
Aminolysis of Esters / 8.6.:
Amide Hydrolysis / 8.7.:
Acylation of Nucleophilic Oxygen and nitrogen Groups / 8.8.:
Intramolecular Catalysis / 8.9.:
Aromaticity / Chapter 9.:
The Concept of Aromaticity / 9.1.:
The Annulenes / 9.2.:
Aromaticity in Charged Rings / 9.3.:
Homoaromaticity / 9.4.:
Fused-Ring Systems / 9.5.:
Heterocyclic Rings / 9.6.:
Aromatic Substitution / Chapter 10.:
Electrophilic Aromatic Substitution Reactions / 10.1.:
Structure-Reactivity Relationships / 10.2.:
Reactivity of Polycyclic and Heteroaromatic Compounds / 10.3.:
Specific Substitution Mechanisms / 10.4.:
Nitration / 10.4.1.:
Halogenation / 10.4.2.:
Protonation and Hydrogen Exchange / 10.4.3.:
Friedel-Crafts Alkylation and Related Reactions / 10.4.4.:
Friedel-Crafts Acylation and Related Reactions / 10.4.5.:
Coupling with Diazonium Compounds / 10.4.6.:
Substitution of Groups Other Than Hydrogen / 10.4.7.:
Nucleophilic Aromatic Substitution by the Addition-Elimination Mechanism / 10.5.:
Nucleophilic Aromatic Substitution by the Elimination-Addition Mechanism / 10.6.:
Concerted Pericyclic Reactions / Chapter 11.:
Electrocyclic Reactions / 11.1.:
Sigmatropic Rearrangements / 11.2.:
Cycloaddition Reactions / 11.3.:
Free-Radical Reactions / Chapter 12.:
Generation and Characterization of Free Radicals / 12.1.:
Background / 12.1.1.:
Stable and Persistent Free Radicals / 12.1.2.:
Direct Detection of Radical Intermediates / 12.1.3.:
Sources of Free Radicals / 12.1.4.:
Structural and Stereochemical Properties of Radical Intermediates / 12.1.5.:
Charged Radical Species / 12.1.6.:
Characteristics of Reaction Mechanisms Involving Radical Intermediates / 12.2.:
Kinetic Characteristics of Chain Reactions / 12.2.1.:
Free-Radical Substitution Reactions / 12.2.2.:
Oxidation / 12.3.1.:
Free-Radical Addition Reactions / 12.4.:
Addition of Hydrogen Halides / 12.4.1.:
Addition of Halomethanes / 12.4.2.:
Addition of Other Carbon Radicals / 12.4.3.:
Addition of Thiols and Thiocarboxylic Acids / 12.4.4.:
Halogen, Sulfur, and Selenium Group Transfer Reactions / 12.5.:
Intramolecular Free-Radical Reactions / 12.6.:
Rearrangement and Fragmentation Reactions of Free Radicals / 12.7.:
Rearrangement Reactions / 12.7.1.:
Fragmentation / 12.7.2.:
Electron-Transfer Reactions Involving Transition-Metal Ions / 12.8.:
S[subscript RN]1 Substitution Processes / 12.9.:
Photochemistry / Chapter 13.:
General Principles / 13.1.:
Orbital Symmetry Considerations Related to Photochemical Reactions / 13.2.:
Photochemistry of Carbonyl Compounds / 13.3.:
Photochemistry of Alkenes and Dienes / 13.4.:
Photochemistry of Aromatic Compounds / 13.5.:
References to Problems
Index
Chemical Bonding and Structure / Chapter 1.:
Valence Bond Description of Chemical Bonding / 1.1.:
Orbital Hybridization / 1.1.1.:
7.

図書

図書
Zerong Wang
出版情報: Hoboken, N.J. : John Wiley & Sons, c2009  3 v. (xlix, 3661 p.) ; 26 cm
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Preface
Acknowledgments
Autobiography
Chemical Abbreviations
Abnormal Claisen Rearrangement / Part 1:
Acetoacetic Ester Condensation / 2:
Acetoacetic Ester Synthesis / 3:
Acyloin Condensation / 4:
Acyloin Rearrangement / 5:
Adkins Catalyst / 6:
Ainley and King Synthesis / 7:
Akabori Amino Acid Reaction / 8:
Albright-Goldman Oxidation / 9:
Alder Ene Reaction / 10:
Alder-Rickert Reaction / 11:
Aldol Reaction and Aldol Condensation / 12:
Algar-Flynn-Oyamada (AFO) Reaction / 13:
Alkene Metathesis / 14:
Allan-Robinson Condensation / 15:
Allylic Rearrangement / 16:
Amadori Rearrangement / 17:
Andrussow Process / 18:
Angeli-Remini Reaction / 19:
ANRORC Rearrangement / 20:
Anschutz Anthracene Synthesis / 21:
Appel Reaction / 22:
Arens-Van Dorp Reaction / 23:
Arndt-Eistert Synthesis / 24:
Asinger Reaction / 25:
Aston-Greenburg Rearrangement / 26:
Atherton-Todd Reaction / 27:
Auwers-Skita Rule / 28:
Aza-Claisen Rearrangement / 29:
Baddeley Isomerization / 30:
Baeyer Diarylmethane Synthesis / 31:
Baeyer-Drewson Reaction / 32:
Baeyer Indole Synthesis / 33:
Baeyer Oxindole Synthesis / 34:
Baeyer Pyridine Synthesis / 35:
Baeyer-Villiger Oxidation / 36:
Bailey Peptide Synthesis / 37:
Bakelite Process / 38:
Baker-Ollis Sydnones Synthesis / 39:
Baker-Venkataraman Rearrangement / 40:
Ball-Goodwin-Morton Oxidation / 41:
Bally-Scholl Reaction / 42:
Balsohn Alkylation / 43:
Balz-Schiemann Reaction / 44:
Bamberger Rearrangement / 45:
Bamford-Stevens Reaction / 46:
Barbier Reaction / 47:
Barbier-Wieland Degradation / 48:
Bardhan Sengupta Synthesis / 49:
Bargellini Condensation / 50:
Bart Reaction / 51:
Bartoli Indole Synthesis / 52:
Barton Decarboxylation / 53:
Barton Deoxygenation / 54:
Barton Reaction / 55:
Barton-Kellogg Olefination / 56:
Barton-Zard Pyrrole Synthesis / 57:
Batcho-Leimgruber Indole Synthesis / 58:
Baudisch Reaction / 59:
Baumann-Fromm Thiophene Synthesis / 60:
Baumgarten ?-Amino Ketone Synthesis / 61:
Baylis-Hillman Reaction / 62:
B´echamp Reduction / 63:
Beckmann Rearrangement and Beckmann Fragmentation / 64:
Bedoukian Halogenation / 65:
B´ehal-Sommelet Rearrangement / 66:
Beirut Reaction / 67:
Bellus-Claisen Rearrangement / 68:
B´enary Reaction / 69:
Benkeser Reduction / 70:
Benzidine Rearrangement / 71:
Benzilic Acid Rearrangement / 72:
Benzoin Condensation / 73:
Bergius Process / 74:
Bergman Cyclization / 75:
Bergmann Degradation / 76:
Bergmann-Stern Azlactone Synthesis / 77:
Bergmann-Zervas Peptide Synthesis / 78:
Bernthsen Reaction / 79:
Berti Olefination / 80:
Bertram-Walbaum Reaction / 81:
Betti Reaction / 82:
Biginelli Reaction / 83:
Birch Reduction / 84:
Birckenbach-Goubeau Halogenation / 85:
Birnbaum-Simonini Reaction / 86:
Bischler Reaction / 87:
Bischler-Napieralski Isoquinoline Synthesis / 88:
Black Rearrangement / 89:
Blaise Ketone Synthesis / 90:
Blaise Reaction / 91:
Blanc Chloromethylation / 92:
Blanc Rule / 93:
Blomquist Cyclic Ketone Synthesis / 94:
Bobbitt Reaction / 95:
Bodroux Amide Synthesis / 96:
Bodroux-Chichibabin Reaction / 97:
B¿oeseken Oxidation / 98:
Bogert-Cook Synthesis / 99:
Bohn-Schmidt Reaction / 100:
Boord Olefin Synthesis / 101:
Borsche-Berkhout Reaction / 102:
Borsche-Drechsel Reaction / 103:
Borsche-Koelsch Cinnoline Synthesis / 104:
Bougault Reaction / 105:
Boulton-Katritzky Rearrangement / 106:
Bourgel Alkyne Synthesis / 107:
Bouveault Aldehyde Synthesis / 108:
Bouveault-Blanc Reduction / 109:
Boyland-Sims Oxidation / 110:
Bradsher Cyclization / 111:
Bradsher Cycloaddition / 112:
Bradsher Pyridinium Salt Synthesis / 113:
Brandi-Guarna Reaction / 114:
Breckpot ?-Lactam Synthesis / 115:
Bredt's Rule / 116:
Brook Rearrangement / 117:
Brown Hydroboration / 118:
Bruckner Isoquinoline Synthesis / 119:
Bucherer Carbazole Synthesis / 120:
Bucherer Reaction / 121:
Bucherer-Bergs Hydantoin Synthesis / 122:
B¿uchner Ring Expansion / 123:
B¿uchner-Curtius-Schlotterbeck Reaction / 124:
Buchwald Indoline Synthesis / 125:
Buchwald-Hartwig Amination / 126:
Burton Trifluoromethylation / 127:
Cadogan-Sundberg Indole Synthesis / 128:
Caglioti Reaction / 129:
Cahours-Hofmann Reaction / 130:
Camps Reaction / 131:
Cannizzaro Reaction / 132:
Carboni-Lindsey Reaction / 133:
Carroll Rearrangement / 134:
Castro Indole Synthesis / 135:
Castro-Stephens Coupling / 136:
Chan Rearrangement / 137:
Chapman Rearrangement / 138:
Chichibabin Amination / 139:
Chichibabin Pyridine Synthesis / 140:
Chretien-Longi Reaction / 141:
Chugaev Reaction / 142:
Ciamician-Dennstedt Reaction / 143:
Claisen Rearrangement / 144:
Claisen-Schmidt Condensation / 145:
Clauson-Kaas Reaction / 146:
Clay-Kinnear-Perren Condensation / 147:
Clayton-Jensen Chlorophosphonation / 148:
Clemmensen Reduction / 149:
Cohen Reductive Lithiation / 150:
Combes Quinoline Synthesis / 151:
Conrad-Limpach Quinoline Synthesis / 152:
Cope Elimination / 153:
Cope Rearrangement / 154:
Corey-Bakshi-Shibata Reduction / 155:
Corey-Chaykovsky Epoxidation / 156:
Corey-Fuchs Reaction / 157:
Corey-Gilman-Ganem Oxidation / 158:
Corey-Kim Oxidation / 159:
Corey-Kwiatkowski Reaction / 160:
Corey-Link Reaction / 161:
Corey-Schmidt Oxidation / 162:
Corey-Suggs Oxidation / 163:
Corey-Winter Olefination / 164:
Cornforth Rearrangement / 165:
Craig 2-Bromo-Pyridine Synthesis / 166:
Cram's Rule / 167:
Criegee Glycol Oxidation / 168:
Criegee Ozonolysis / 169:
Criegee Rearrangement / 170:
Crum-Brown-Gibson Substitution Rule / 171:
Curtius Rearrangement / 172:
[m+n(+. . . )] Cycloaddition / 173:
[2+2] Cycloaddition / 174:
Dakin Reaction / 175:
Dakin-West Reaction / 176:
Danheiser Annulation / 177:
Darzens Condensation / 178:
Darzens Halogenation / 179:
Darzens Olefin Acylation / 180:
Darzens-Nenitzescu Reaction / 181:
Davidson Oxazole Cyclization / 182:
de Mayo Reaction / 183:
Decker-Becker Secondary Amine Synthesis / 184:
Del´epine Reaction / 185:
Demjanov Rearrangement / 186:
Dess-Martin Periodinane Oxidation / 187:
D-Homo Rearrangement / 188:
Dieckmann Condensation / 189:
Diels-Alder Reaction / 190:
Diels-Reese Reaction / 191:
Dienol-Benzene Rearrangement / 192:
Dienone-Phenol Rearrangement / 193:
Dimroth Rearrangement / 194:
Di-Π-Methane Rearrangement / 195:
1,3-Dipolar Cycloaddition / 196:
Doebner Reaction / 197:
Doebner-Miller Reaction / 198:
Doering-Moore-Skattebøl Reaction / 199:
Dotz Benzannulation / 200:
Dowd-Beckwith Ring Expansion / 201:
Duff Reaction / 202:
Dutt-Wormall Reaction / 203:
Eastwood Olefination / 204:
Eder Reaction / 205:
Edman Degradation / 206:
Eglinton Coupling / 207:
Ehrlich-Sachs Reaction / 208:
Einhorn Acylation / 209:
Einhorn-Brunner Reaction / 210:
Eisleb Alkylation / 211:
Elbs Persulfate Oxidation / 212:
Elbs Reaction / 213:
Eltekoff Hydrolysis / 214:
Emde Degradation / 215:
Emmert Reaction / 216:
Erlenmeyer-plochl Azlactone Synthesis / 217:
Eschenmoser Coupling / 218:
Eschenmoser Fragmentation / 219:
Eschweiler-Clarke Methylation / 220:
Ester Pyrolysis / 221:
E´ tard Reaction / 222:
Evans Aldol Reaction / 223:
Favorskii Rearrangement / 224:
Favorskii-Babayan Reaction / 225:
Feist-Benary Reaction / 226:
Fenton Reaction / 227:
Ferrier Reaction / 228:
Ferrier-II Rearrangement / 229:
F´etizon Oxidation / 230:
Finkelstein Reaction / 231:
Fischer Carbene Complexes / 232:
Fischer Indole Synthesis / 233:
Fischer Oxazole Synthesis / 234:
Fischer Phenylhydrazine Synthesis / 235:
Fischer Phenylhydrazone and Osazone Synthesis / 236:
Fischer-Helferich Glycosylation / 237:
Fischer-Hepp Rearrangement / 238:
Fischer-Speier Esterification / 239:
Fischer-Tropsch Synthesis / 240:
Fleming-Tamao Oxidation / 241:
Flood Reaction / 242:
Forster Reaction / 243:
Franchimont Condensation / 244:
Frankland Reaction / 245:
Fr´ater-Seebach Alkylation / 246:
Freund Reaction / 247:
Friedel-Crafts Acylation / 248:
Friedel-Crafts Alkylation / 249:
Friedl¿ander Condensation / 250:
Fries Rearrangement / 251:
Fritsch-Buttenberg-Wiechell Rearrangement / 252:
Fujimoto-Belleau Reaction / 253:
Fukuyama Amine Synthesis / 254:
Fukuyama Indole Synthesis / 255:
F¿urstner Indole Synthesis / 256:
Gabriel Primary Amine Synthesis / 257:
Gabriel Reaction / 258:
Gabriel-Colman Rearrangement / 259:
Garner Aldehyde / 260:
Gassman Indole Synthesis / 261:
Gassman Oxindole Synthesis / 262:
Gassman Reaction / 263:
Gattermann Aldehyde Synthesis / 264:
Gattermann Reaction / 265:
Gattermann-Koch Formylation / 266:
Gewald Reaction / 267:
Ghosez Cyclization / 268:
Ghosez Keteniminium-Olefin Cyclization / 269:
Gibbs-Wohl Naphthalene Oxidation / 270:
Gilman-Cason Ketone Synthesis / 271:
Gilman-Speeter Reaction / 272:
Gomberg Free Radical Reaction / 273:
Gomberg-Bachmann Pinacol Synthesis / 274:
Gomberg-Bachmann Reaction / 275:
Gould-Jacobs Reaction / 276:
Graebe-Ullmann Synthesis / 277:
Gr¿anacher Synthesis / 278:
Gribble Reductive Amination / 279:
Griess Diazotization / 280:
Grignard Degradation / 281:
Grignard Reaction / 282:
Grob Fragmentation / 283:
Grosheintz-Fischer-Reissert Aldehyde Synthesis / 284:
Grundmann Aldehyde Synthesis / 285:
Gryszkiewicz-Trochimowski and Mccombie Fluorination / 286:
Guareschi Reaction / 287:
Guerbet Condensation / 288:
Gutknecht Condensation / 289:
Hajos-Parrish-Eder-Sauer-Wiechert Reaction / Part 2:
Haller-Bauer Cleavage / 291:
Hammick Reaction / 292:
Hansley-Prelog Acyloin Condensation / 293:
Hantzsch Dihydropyridine Synthesis / 294:
Hantzsch Pyrrole Synthesis / 295:
Hantzsch Thiazole Synthesis / 296:
Hass-Bender Oxidation / 297:
Haworth Methylation / 298:
Haworth Synthesis / 299:
Hayashi Rearrangement / 300:
Heck Reaction / 301:
Hegedus Indole Synthesis / 302:
Helferich Condensation / 303:
Helferich Glycosylation / 304:
Hell-Volhard-Zelinsky Reaction / 305:
Hemetsberger Indole Synthesis / 306:
Henkel Reaction / 307:
Henry Reaction / 308:
Herbst-Engel Transamination / 309:
Heron Rearrangement / 310:
Herz Reaction / 311:
Heumann Indigo Process / 312:
Heyns Rearrangement / 313:
Hilbert-Johnson Reaction / 314:
Hinsberg Oxindole Synthesis / 315:
Hinsberg Reaction / 316:
Hinsberg Sulfone Synthesis / 317:
Hinsberg Thiophene Synthesis / 318:
Hiyama Coupling / 319:
Hoch-Campbell Reaction / 320:
Hock Rearrangement / 321:
Hofer-Moest Reaction / 322:
Hofmann Degradation / 323:
Hofmann Elimination / 324:
Hofmann Isonitrile Synthesis / 325:
Hofmann Rule / 326:
Hofmann-Loffler-Freytag Reaction / 327:
Hofmann-Martius Rearrangement / 328:
Hofmann-Sand Reaction / 329:
Hooker Oxidation / 330:
Horenstein-P¿ahlicke Reaction / 331:
Horner-Wadsworth-Emmons Olefination / 332:
Hosomi-Sakurai Allylation / 333:
Houben-Hoesch Reaction / 334:
Houdry Cracking Process / 335:
Huisgen Pyrrole Synthesis / 336:
Hunsdiecker Condensation / 337:
Hunsdiecker Reaction / 338:
Hydroformylation / 339:
Iodolactonization / 340:
Irvine-Purdie Methylation / 341:
Jacobsen Rearrangement / 342:
Jacobsen-Katsuki Epoxidation / 343:
Janovsky Reaction / 344:
Japp-Klingemann Fischer Indole Synthesis / 345:
Japp-Klingemann Reaction / 346:
Japp-Maitland Condensation / 347:
Johnson Orthoester Claisen Rearrangement / 348:
Jones Oxidation / 349:
Jourdan-Ullmann Reaction / 350:
Julia Olefination / 351:
Juli´a-Colonna Asymmetric Epoxidation / 352:
Kabachnik-Fields Reaction / 353:
Kahne Glycosylation / 354:
Keck Allylation / 355:
Keck Macrolactonization / 356:
Kemp Elimination / 357:
Kennedy Oxidative Cyclization / 358:
Kiliani-Fischer Cyanohydrin Synthesis / 359:
Kishner Decomposition / 360:
Knoevenagel Condensation / 361:
Knoevenagel Diazotization Method / 362:
Knorr Pyrazole Synthesis / 363:
Knorr Pyrrole Synthesis / 364:
Knorr Quinoline Synthesis / 365:
Koch-Haaf Carboxylation / 366:
Kochi Reaction / 367:
Koenigs-Knorr Reaction / 368:
Kolbe Electrolysis / 369:
Kolbe Nitrile Synthesis / 370:
Kolbe-Schmidt Reaction / 371:
Kondrat'eva Pyridine Synthesis / 372:
Kornblum Oxidation / 373:
Kornblum-Delamare Rearrangement / 374:
Kostanecki-Robinson Reaction / 375:
Kowalski Ester Homologation / 376:
Krapcho Decarboxylation / 377:
Kriewitz Condensation / 378:
Kr¿ohnke Pyridine Synthesis / 379:
Kuhn-Roth Oxidation / 380:
Kuhn-Winterstein Reduction / 381:
Kulinkovich Cyclopropanation / 382:
Kutscheroff Acetylene Hydration / 383:
Lander Rearrangement / 384:
Larock Indole Synthesis / 385:
Lawesson's Reagent / 386:
Lebedev Process / 387:
Lehmstedt-Tanasescu Reaction / 388:
Lemieux-Johnson Oxidation / 389:
Leuckart Reaction / 390:
Leuckart Thiophenol Synthesis / 391:
Levinstein Process / 392:
Lieben Iodoform Reaction / 393:
Liebeskind-Srogl Cross-Coupling / 394:
Lindlar Hydrogenation / 395:
Lobry de Bruyn-Alberda van Ekenstein Transformation / 396:
Lombardo Methylenation / 397:
Lossen Rearrangement / 398:
Luche Reaction / 399:
Luche Reduction / 400:
MacDonald-Fischer Degradation / 401:
Madelung Indole Synthesis / 402:
Maillard Reaction / 403:
Maitland-Japp Reaction / 404:
Majetich Annulation / 405:
Malaprade Reaction / 406:
Malonic Ester Synthesis / 407:
Mandelic Acid Synthesis / 408:
Mannich Reaction / 409:
Marckwald Asymmetric Synthesis / 410:
Markownikoff Rule and Anti-Markownikoff Rule / 411:
Martinet Reaction / 412:
Martin's Sulfurane / 413:
Mattox-Kendall Reaction / 414:
McCormack Cycloaddition / 415:
McFadyen-Stevens Reaction / 416:
McLafferty Rearrangement / 417:
McMurry Coupling / 418:
Meerwein Arylation / 419:
Meerwein-Ponndorf-Verley Reduction / 420:
Meerwein's Salt / 421:
Meinwald Rearrangement / 422:
Meisenheimer Complexes / 423:
Meisenheimer Rearrangement / 424:
Menke Nitration / 425:
Menschutkin Reaction / 426:
Mentzer Pyrone Synthesis / 427:
Merrifield Solid-Phase Peptide Synthesis / 428:
Meyer-Hartmann Reaction / 429:
Meyers Aldehyde Synthesis / 430:
Meyer-Schuster Rearrangement / 431:
Michael Addition / 432:
Michaelis-Arbuzov Rearrangement / 433:
Michael-Stetter Reaction / 434:
Miescher Degradation / 435:
Mignonac Reaction / 436:
Milas Hydroxylation / 437:
Mislow-Evans Rearrangement / 438:
Mitsunobu Reaction / 439:
Moffatt-Swern Oxidation / 440:
Moore Cyclization / 441:
Morgan-Walls Cyclization / 442:
Mori-Ban Indole Synthesis / 443:
Morin Rearrangement / 444:
Mosher's Acid / 445:
Moureau-Mignonac Ketimine Synthesis / 446:
Mukaiyama Aldol Reaction / 447:
Mukaiyama-Michael Reaction / 448:
M¿ uller-Cunradi-Pieroh Process / 449:
Myers-Saito Cyclization / 450:
Nagata Reaction / 451:
Nazarov Cyclization / 452:
Neber Rearrangement / 453:
Neber-Bossel Synthesis / 454:
Nef Reaction / 455:
Negishi Cross-Coupling / 456:
Nencki Reaction / 457:
Nenitzescu Synthesis / 458:
Nenitzescu Indole Synthesis / 459:
Newman-Kwart Rearrangement / 460:
Nicholas Reaction / 461:
Niementowski Reaction / 462:
Nierenstein Reaction / 463:
Norrish Type I Reaction / 464:
Norrish Type II Reaction / 465:
Noyori Hydrogenation / 466:
Nozaki-Hiyama-Kishi Reaction / 467:
Nysted Reagent / 468:
Ohle Quinoxaline Synthesis / 469:
Oppenauer Oxidation / 470:
Orton Rearrangement / 471:
Ostromislensky Process / 472:
Overman Rearrangement / 473:
Paal-Knorr Furan Synthesis / 474:
Paal-Knorr Pyrrole Synthesis / 475:
Paneth Technique / 476:
Parham Cyclization / 477:
Parikh-Doering Oxidation / 478:
Passerini Reaction / 479:
Paterno-Buchi Reaction / 480:
Pauson-Khand Reaction / 481:
Payne Rearrangement / 482:
Pearlman's Catalyst / 483:
Pechmann Pyrazole Synthesis / 484:
Pechmann Reaction / 485:
Pellizzari Reaction / 486:
Perkin Reaction / 487:
Perkin Synthesis / 488:
Perkow Reaction / 489:
Petasis-Ferrier Rearrangement / 490:
Peterson Olefination / 491:
Petrenko-Kritschenko Piperidone Synthesis / 492:
Pfau-Plattner Azulene Synthesis / 493:
Pfitzinger Reaction / 494:
Pfitzner-Moffatt Oxidation / 495:
Phillips-Ladenburg Benzimidazole Synthesis / 496:
Photo-Fries Rearrangement / 497:
Pictet-Gams Synthesis / 498:
Pictet-Spengler Reaction / 499:
Piloty-Robinson Pyrrole Synthesis / 500:
Pinacol Coupling Reaction / 501:
Pinacol Rearrangement / 502:
Pinner Condensation / 503:
Pinner Reaction / 504:
Pinner S-Triazine Synthesis / 505:
Piria Reaction / 506:
Plancher Rearrangement / 507:
Polonovski Reaction / 508:
Pomeranz-Fritsch Reaction / 509:
Ponzio Reaction / 510:
Pr´evost Reaction / 511:
Prey Ether Cleavage / 512:
Prilezhaev Reaction / 513:
Prins Reaction / 514:
Pudovik Reaction / 515:
Pummerer Rearrangement / 516:
Quelet Reaction / 517:
Radziszewski Reaction / Part THREE.:
Ramberg-B¿acklund Reaction / 519:
Raney Nickel / 520:
Rauhut-Currier Reaction / 521:
Reed Reaction / 522:
Reformatsky Reaction / 523:
Regitz Diazo Transfer / 524:
Reilly-Rickinbottom Rearrangement / 525:
Reimer-Tiemann Reaction / 526:
Reissert Compound / 527:
Reissert Indole Synthesis / 528:
Reppe Alkyne Cyclotrimerization / 529:
Reppe Carbonylation / 530:
Reppe Cyclization / 531:
Reppe Vinylation / 532:
Retro-Diels-Alder Reaction / 533:
Retro-Ene Reaction / 534:
Retropinacol Rearrangement / 535:
Reverdin Rearrangement / 536:
Riehm Quinoline Synthesis / 537:
Rieke Metal / 538:
Riemenschneider Reaction / 539:
Riley Oxidation / 540:
Ritter Reaction / 541:
Robinson Annulation / 542:
Robinson-Gabriel Oxazole Synthesis / 543:
Robinson-Schopf Condensation / 544:
Rosenmund Reaction / 545:
Rosenmund Reduction / 546:
Rosenmund-von Braun Reaction / 547:
Rothemund Reaction / 548:
Roush Crotylboration / 549:
Rowe Rearrangement / 550:
Rubottom Oxidation / 551:
Ruff Degradation / 552:
Rupe Rearrangement / 553:
Sabatier-Senderens Reduction / 554:
Saegusa Cyclization / 555:
Saegusa Oxidation / 556:
Sandmeyer Isatin Synthesis / 557:
Sandmeyer Reaction / 558:
Sarett Oxidation / 559:
Saytzeff Rule / 560:
Schiff Base / 561:
Schlack-Kumpf Reaction / 562:
Schlotterbeck Reaction / 563:
Schmidlin Ketene Synthesis / 564:
Schmidt Glycosylation / 565:
Schmidt Reaction / 566:
Schmidt-Rutz Reaction / 567:
Schmittel Cyclization / 568:
Scholl Reaction / 569:
Sch¿ollkopf Bis-Lactim Ether Method / 570:
Sch¿ollkopf Oxazole Synthesis / 571:
Sch¿onberg Rearrangement / 572:
Schotten-Baumann Reaction / 573:
Schwartz Reagent / 574:
Screttas Lithiation / 575:
Selenoxide Elimination / 576:
Semmler-Wolff Aromatization / 577:
Serini Reaction / 578:
Seyferth-Gilbert Homologation / 579:
Shapiro Reaction / 580:
Sharpless Aminohydroxylation / 581:
Sharpless Dihydroxylation / 582:
Sharpless Epoxidation / 583:
Shechter-Kaplan Oxidative Nitration / 584:
Shi Epoxidation / 585:
Simmons-Smith Reaction / 586:
Simonini Reaction / 587:
Skraup Reaction / 588:
Smiles Rearrangement / 589:
Sommelet Reaction / 590:
Sommelet-Hauser Rearrangement / 591:
Sonn-Muller Reaction / 592:
Sonogashira Coupling / 593:
Staudinger [2+2] Cycloaddition / 594:
Staudinger Reaction / 595:
Stec Reaction / 596:
Steglich Catalyst / 597:
Steglich Rearrangement / 598:
Stephen Reaction / 599:
Stetter Reaction / 600:
Stevens Rearrangement / 601:
Stieglitz Rearrangement / 602:
Stille Coupling / 603:
Stobbe Condensation / 604:
Stolle-Becker Synthesis / 605:
Stork Reaction / 606:
Strecker Degradation / 607:
Strecker Reaction / 608:
Strecker Synthesis / 609:
Su´arez Cleavage / 610:
Sugasawa Indole Synthesis / 611:
Sugasawa Reaction / 612:
Sundberg Indole Synthesis / 613:
Suzuki Coupling / 614:
Swarts Reaction / 615:
Takai Olefination / 616:
Tebbe Olefination / 617:
ter Meer Reaction / 618:
Thiele-Winter Acetoxylation / 619:
Thorpe-Ziegler Cyclization / 620:
Tiemann Cyanohydrin Amination / 621:
Tiemann Rearrangement / 622:
Tiffeneau-Demjanov Ring Expansion / 623:
Tishchenko Reaction / 624:
Traube Purine Synthesis / 625:
Trofimov Reaction / 626:
Trost Desymmetrization / 627:
Truce-Smiles Rearrangement / 628:
Tscherniac-Einhorn Reaction / 629:
Tsuji-Trost Reaction / 630:
Twitchell Process / 631:
Tyrer Process / 632:
Ueno-Stork Cyclization / 633:
Ugi Reaction / 634:
Ullmann Acridine Synthesis / 635:
Ullmann Coupling / 636:
Ullmann Diaryl Ether Synthesis / 637:
Urech Cyanohydrin Method.Synthesis / 638:
van Slyke Method / 640:
Varrentrapp Reaction / 641:
Victor Meyer Reaction / 642:
Vilsmeier Formylation / 643:
Vinylcyclopropane Rearrangement / 644:
Voigt Reaction / 645:
von Auwers Rearrangement / 646:
von Braun Cyanogen Bromide Reaction / 647:
von Braun Degradation / 648:
von Braun-Rudolf Synthesis / 649:
von Richter Cinnoline Synthesis / 650:
von Richter Reaction / 651:
Vorbr¿uggen Glycosylation / 652:
Wacker Oxidation / 653:
Wagner-Jauregg Reaction / 654:
Wagner-Meerwein Rearrangement / 655:
Walden Inversion / 656:
Wallach Rearrangement / 657:
Weerman Reaction / 658:
Weidenhagen Synthesis / 659:
Weinreb Amide Formation / 660:
Weinreb Ketone Synthesis / 661:
Weiss-Cook Condensation / 662:
Weitz-Scheffer Epoxidation / 663:
Wender Indole Synthesis / 664:
Wessely-Moser Rearrangement / 665:
Westphalen Rearrangement / 666:
Wharton Rearrangement / 667:
Wibaut-Arens Alkylation / 668:
Wichterle Reaction / 669:
Widman-Stoermer Synthesis / 670:
Wilkinson's Catalyst / 671:
Willgerodt-Kindler Reaction / 672:
Williamson Ether Synthesis / 673:
Wittig Reaction / 674:
[1,2]-Wittig Rearrangement / 675:
[2,3]-Wittig Rearrangement / 676:
Wohl Degradation / 677:
Wohl-Aue Reaction / 678:
W¿ohler Synthesis / 679:
Wohl-Ziegler Bromination / 680:
Wolff Rearrangement / 681:
Wolffenstein-B¿oters Reaction / 682:
Wolff-Kishner Reduction / 683:
Woodward Cis-Hydroxylation / 684:
Wurtz Synthesis / 685:
Wurtz-Fittig Reaction / 686:
Yamada Coupling / 687:
Yamaguchi Esterification / 688:
Zeisel Determination / 689:
Zelinsky-Stadnikoff Reaction / 690:
Zempl´en Deacetylation / 691:
Zerewitinoff Determination / 692:
Ziegler Alcohol Synthesis / 693:
Ziegler-Hafner Azulene Synthesis / 694:
Ziegler-Natta Polymerization / 695:
Zimmermann Reaction / 696:
Zincke Disulfide Cleavage / 697:
Zincke Nitration / 698:
Zincke Reaction / 699:
Zincke-Suhl Reaction / 700:
Zinke Synthesis / 701:
Appendixes
Schematic Reaction Index
Reaction Type Summary
Summary of Initial Publications on Named Reactions
Journal Abbreviation
The Statistics of Reaction Published Years
Subject Index
Preface
Acknowledgments
Autobiography
8.

図書

図書
L.G. Wade, Jr
出版情報: Upper Saddle River, N.J. ; Tokyo : Pearson Prentice Hall, c2010  xxviii, 1262, 7, 1, 12 p., [4] p. of plates ; 27 cm
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9.

図書

図書
Gokel, George W., 1946- ; Dean, John Aurie, 1921-
出版情報: New York : McGraw-Hill Education , London : McGraw-Hill[m], 2003  800 p ; 23cm
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10.

図書

図書
Maitland Jones, Jr
出版情報: New York : W.W. Norton, c2005  xxxvi, 1323, 62 p. ; 27 cm.
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Preface
Introduction
Atoms and Molecules; Orbitals and Bonding / Chapter 1.:
Atoms and Atomic Orbitals / 1.1:
Covalent Bonds and Lewis Structures / 1.2:
Introduction to Resonance Forms / 1.3:
More on Atomic Orbitals / 1.4:
The Covalent Bond: Hydrogen (H[subscript 2]) / 1.5:
Bond Strength / 1.6:
An Introduction to Reactivity: Acids and Bases / 1.7:
Quantum Mechanics and Babies / 1.8:
Summary / 1.9:
Additional Problems / 1.10:
Alkanes / Chapter 2.:
The Structure of Methane (CH[subscript 4]) / 2.1:
Hybrid Orbitals: Making a Better Model for Methane / 2.2:
Derivatives of Methane: Methyl (CH[subscript 3]) and Methyl Compounds (CH[subscript 3]X) / 2.3:
The Methyl Cation ([superscript +]CH[subscript 3]), Anion ([superscript -]:CH[subscript 3]), and Radical (.CH[subscript 3]) / 2.4:
Ethane (C[subscript 2]H[subscript 6]), Ethyl Compounds (C[subscript 2]H[subscript 5]X), and Newman Projections / 2.5:
Structure Drawings / 2.6:
Propane (C[subscript 3]H[subscript 8]) and Propyl Compounds (C[subscript 3]H[subscript 7]X) / 2.7:
Butanes (C[subscript 4]H[subscript 10]), Butyl Compounds (C[subscript 4]H[subscript 9]X), and Conformational Analysis / 2.8:
Pentanes (C[subscript 5]H[subscript 12]) and Pentyl Compounds (C[subscript 5]H[subscript 11]X) / 2.9:
The Naming Conventions for Alkanes / 2.10:
Writing Isomers / 2.11:
Rings / 2.12:
Physical Properties of Alkanes and Cycloalkanes / 2.13:
[superscript 13]C Nuclear Magnetic Resonance Spectroscopy / 2.14:
Alkanes as Biomolecules / 2.15:
Alkenes and Alkynes / 2.16:
Alkenes: Structure and Bonding / 3.1:
Derivatives, Isomers, and Names of Alkenes / 3.2:
Nomenclature / 3.3:
The Cahn-Ingold-Prelog Priority System / 3.4:
Relative Stability of Alkenes: Heats of Formation / 3.5:
Double Bonds in Rings / 3.6:
Physical Properties of Alkenes / 3.7:
Alkynes: Structure and Bonding / 3.8:
Relative Stability of Alkynes: Heats of Formation / 3.9:
Derivatives and Isomers of Alkynes / 3.10:
Triple Bonds in Rings / 3.11:
Physical Properties of Alkynes / 3.12:
Acidity of Alkynes / 3.13:
Molecular Formulas and Degrees of Unsaturation / 3.14:
Alkenes and Biology / 3.15:
Stereochemistry / 3.16:
Chirality / 4.1:
Properties of Enantiomers: Physical Differences / 4.2:
The (R/S) Convention / 4.3:
The Physical Basis of Optical Activity / 4.4:
Properties of Enantiomers: Chemical Differences / 4.5:
Interconversion of Enantiomers by Mobile Equilibria: Gauche Butane / 4.6:
Diastereomers: Molecules Containing More Than One Stereogenic Atom / 4.7:
Physical Properties of Diastereomers: Optical Resolution / 4.8:
Determination of Absolute Configuration (R or S) / 4.9:
Stereochemical Analysis of Ring Compounds (a Beginning) / 4.10:
Review of Isomerism / 4.11:
Chirality without "Four Different Groups Attached to One Carbon" / 4.12:
Stereochemistry in the Real World: Thalidomide; The Consequences of Being Wrong-Handed / 4.13:
Rings and Strain / 4.14:
Quantitative Evaluation of Strain Energy / 5.2:
Stereochemistry of Cyclohexane: Conformational Analysis / 5.3:
Monosubstituted Cyclohexanes / 5.4:
Disubstituted Ring Compounds / 5.5:
Bicyclic Compounds / 5.6:
Polycyclic Systems / 5.7:
Adamantanes in Materials and Biology / 5.8:
Substitution and Elimination Reactions: The S[subscript N]2, S[subscript N]1, E2, and E1 Reactions / 5.9:
Alkyl Halides: Nomenclature and Structure / 6.1:
Reaction Mechanism: Br[o slash]nsted Acids and Bases / 6.2:
The Arrow Formalism / 6.3:
Lewis Acids and Bases / 6.4:
HOMO-LUMO Interactions / 6.5:
Reactions of Alkyl Halides: The Substitution Reaction / 6.6:
Substitution, Nucleophilic, Bimolecular: The S[subscript N]2 Reaction / 6.7:
The S[subscript N]2 Reaction in Biochemistry / 6.8:
Substitution, Nucleophilic, Unimolecular: The S[subscript N]1 Reaction / 6.9:
Overview of the S[subscript N]2 and S[subscript N]1 Reactions / 6.10:
The Unimolecular Elimination Reaction: E1 / 6.11:
The Bimolecular Elimination Reaction: E2 / 6.12:
What Can We Do with These Reactions? Synthetic Utility / 6.13:
Equilibria / 6.14:
Equilibrium / 7.1:
Gibbs Standard Free Energy Change / 7.2:
Rates of Chemical Reactions / 7.3:
Rate Constant / 7.4:
Energy Barriers in Chemical Reactions: The Transition State and Activation Energy / 7.5:
Reaction Mechanism / 7.6:
The Hammond Postulate: Thermodynamics versus Kinetics / 7.7:
Enzymes and Reaction Rates / 7.8:
Additions to Alkenes 1 / 7.9:
Electronegativity / 8.1:
Mechanism of the Addition of Hydrogen Halides to Alkenes / 8.2:
Regiochemistry / 8.3:
Resonance Effects / 8.4:
Review of Resonance: How to Write Resonance Forms / 8.5:
Resonance and the Stability of Carbocations / 8.6:
Inductive Effects on Addition Reactions / 8.7:
H--X Addition Reactions: Hydration / 8.8:
Dimerization and Polymerization of Alkenes / 8.9:
Hydroboration / 8.10:
Utility of Hydroboration: Alcohol Formation / 8.11:
Rearrangements During H--X Addition to Alkenes / 8.12:
Rearrangements in Biological Processes / 8.13:
Additions to Alkenes 2; Additions to Alkynes / 8.14:
Addition of X[subscript 2] Reagents / 9.1:
Hydration Through Mercury Compounds: Oxymercuration / 9.2:
Other Addition Reactions Involving Three-Membered Rings: Oxiranes and Cyclopropanes / 9.3:
Dipolar Addition Reactions / 9.4:
Addition Reactions of Alkynes: H--X Addition / 9.5:
Addition of X[subscript 2] Reagents to Alkynes / 9.6:
Hydration of Alkynes / 9.7:
Hydroboration of Alkynes / 9.8:
Hydrogenation of Alkynes: Syn Hydrogenation / 9.9:
Reduction by Sodium in Ammonia: Anti Hydrogenation / 9.10:
Three-membered Rings in Biochemistry / 9.11:
Radical Reactions / 9.12:
Formation and Simple Reactions of Radicals / 10.1:
Structure of Radicals / 10.2:
Stability of Radicals / 10.3:
Radical Addition to Alkenes / 10.4:
Other Radical Addition Reactions / 10.5:
Radical-Initiated Addition of HBr to Alkynes / 10.6:
Photohalogenation / 10.7:
Allylic Halogenation / 10.8:
Rearrangements (and Nonrearrangements) of Radicals / 10.9:
Radicals in Your Body: Do Free Radicals Age Us? / 10.10:
Dienes and the Allyl System; 2p Orbitals in Conjugation / 10.11:
Allenes: 1,2-Dienes / 11.1:
Related Systems: Ketenes and Cumulenes / 11.2:
Allenes as Intermediates in the Isomerization of Acetylenes / 11.3:
1,3-Dienes / 11.4:
The Physical Consequences of Conjugation / 11.5:
Molecular Orbitals and Ultraviolet Spectroscopy / 11.6:
Polyenes and Vision / 11.7:
The Chemical Consequences of Conjugation: Addition Reactions of Dienes / 11.8:
Thermodynamic and Kinetic Control of Addition Reactions / 11.9:
The Allyl System: Three Overlapping 2p Orbitals / 11.10:
The Allyl Cation: S[subscript N]1 Solvolysis of Allylic Halides / 11.11:
S[subscript N]2 Reactions of Allylic Halides / 11.12:
The Allyl Radical / 11.13:
The Allyl Anion / 11.14:
The Diels-Alder Reaction of Dienes / 11.15:
Biosynthesis of Terpenes / 11.16:
Steroid Biosynthesis / 11.17:
Conjugation and Aromaticity / 11.18:
The Structure of Benzene / 12.1:
A Resonance Picture of Benzene / 12.2:
The Molecular Orbital Picture of Benzene / 12.3:
Quantitative Evaluations of Resonance Stabilization (Delocalization Energy) in Benzene / 12.4:
A Generalization of Aromaticity: Huckel's 4n + 2 Rule / 12.5:
Annulenes / 12.6:
Substituted Benzenes / 12.7:
Physical Properties of Substituted Benzenes / 12.8:
Heterobenzenes and other Heterocyclic Aromatic Compounds / 12.9:
Polynuclear Aromatic Compounds / 12.10:
Introduction to the Chemistry of Benzene / 12.11:
The Benzyl Group and Its Reactivity: Activation of the Adjacent (Benzyl) Position by Benzene Rings / 12.12:
The Bio-downside: The Mechanism of Carcinogenesis by Polycyclic Aromatic Compounds / 12.13:
Substitution Reactions of Aromatic Compounds / 12.14:
Addition Reactions of Benzenes to Give Nonaromatic Compounds: Hydrogenation / 13.1:
Diels-Alder Reactions / 13.2:
Other Addition Reactions / 13.3:
Substitution Reactions of Benzene / 13.4:
Electrophilic Aromatic Substitution / 13.5:
The Friedel-Crafts Alkylation Reaction / 13.6:
Friedel-Crafts Acylation / 13.7:
Stable Carbocations in "Superacid" / 13.8:
Summary of Simple Aromatic Substitution: What We Can Do So Far / 13.9:
Disubstituted Benzenes: Ortho, Meta, and Para Substitution / 13.10:
Inductive Effects in Aromatic Substitution / 13.11:
Polysubstitution of Aromatic Compounds and Synthesis of Multiply Substituted Benzenes / 13.12:
Nucleophilic Aromatic Substitution / 13.13:
Benzyne / 13.14:
Biological Synthesis of Aromatic Rings: Phenylalanine / 13.15:
Analytical Chemistry / 13.16:
Chromatography / 14.1:
Mass Spectrometry / 14.2:
Infrared Spectroscopy / 14.3:
Nuclear Magnetic Resonance Spectroscopy / 14.4:
Survey of NMR Spectra of Organic Molecules / 14.5:
Spin-Spin Coupling: The Coupling Constant, J / 14.6:
More Complicated Spectra / 14.7:
Decoupled Spectra / 14.8:
Nuclear Magnetic Resonance Spectra of Other Nuclei / 14.9:
Determination of the Structure of a Complex Biomolecule: Maitotoxin / 14.10:
Dynamic NMR / 14.11:
Carbonyl Chemistry 1: Addition Reactions / 14.12:
Structure of the Carbon-Oxygen Double Bond / 15.1:
Nomenclature of Carbonyl Compounds / 15.2:
Physical Properties of Carbonyl Compounds / 15.3:
Spectroscopy of Carbonyl Compounds / 15.4:
Reactions of Carbonyl Compounds: Simple Reversible Additions / 15.5:
Equilibrium in Addition Reactions / 15.6:
Other Addition Reactions: Additions of Cyanide and Bisulfite / 15.7:
Addition Reactions Followed by Water Loss: Acetal and Ketal Formation / 15.8:
Addition Reactions of Nitrogen Bases: Imine and Enamine Formation / 15.9:
Organometallic Reagents / 15.10:
Irreversible Addition Reactions / 15.11:
Oxidation of Alcohols to Carbonyl Compounds / 15.12:
The Wittig Reaction / 15.13:
Biological Oxidation / 15.14:
The Chemistry of Alcohols Summarized and Extended: Glycols, Ethers, and Related Sulfur Compounds / 15.15:
Structure of Alcohols / 16.1:
Physical Properties of Alcohols / 16.3:
Spectroscopic Properties of Alcohols / 16.4:
Acid and Base Properties of Alcohols / 16.5:
Reactions of Alcohols / 16.6:
Syntheses of Alcohols / 16.7:
Dialcohols: Diols or Glycols / 16.8:
Ethers / 16.9:
Syntheses of Ethers / 16.10:
Reactions of Ethers / 16.11:
Thiols (Mercaptans) and Thioethers (Sulfides) / 16.12:
Reactions and Syntheses of Thiols and Sulfides / 16.13:
Crown Ethers / 16.14:
Carbonyl Chemistry 2: Reactions at the [alpha]-Position / 16.15:
Aldehydes and Ketones Are Weak Bronsted Acids / 17.1:
Reactions of Enols and Enolates / 17.2:
Condensation Reactions of Carbonyl Compounds: The Aldol Condensation / 17.3:
Reactions Related to the Aldol Condensation / 17.4:
Problem Solving / 17.5:
Carbonyl Compounds without [alpha]-Hydrogens: Magid's Third Rule / 17.6:
The Aldol Condensation in the Real World: Introduction to Modern Synthesis / 17.7:
Carboxylic Acids / 17.8:
Nomenclature and Properties of Carboxylic Acids / 18.1:
Structure of Carboxylic Acids / 18.2:
Infrared and Nuclear Magnetic Resonance Spectra of Carboxylic Acids / 18.3:
Acidity and Basicity of Carboxylic Acids / 18.4:
Reactions of Carboxylic Acids / 18.5:
Reactivity of Carboxylic Acids at the [alpha]-Position / 18.6:
Syntheses of Carboxylic Acids / 18.7:
Fatty Acids / 18.8:
Derivatives of Carboxylic Acids: Acyl Compounds / 18.9:
Physical Properties and Structures of Acyl Compounds / 19.1:
Spectral Characteristics / 19.3:
Reactions of Acid Chlorides / 19.4:
Reactions of Anhydrides / 19.5:
Addition-Elimination Reactions of Esters / 19.6:
Reactions of Amides / 19.7:
Reactions of Nitriles / 19.8:
Reactions of Ketenes / 19.9:
Enolate Chemistry of Esters: The Claisen and Related Condensation Reactions / 19.10:
Variations on the Claisen Condensation / 19.11:
Forward and Reverse Claisen Condensations in Biology / 19.12:
Reactions of [beta]-Keto Esters / 19.13:
Complicated "Fun in Base" Problems / 19.14:
New Synthetic Routes to Acyl Compounds / 19.15:
Thermal Elimination Reactions of Esters / 19.16:
Introduction to the Chemistry of Nitrogen-Containing Compounds: Amines / 19.17:
Structure and Physical Properties of Amines / 20.1:
Spectroscopic Properties of Amines / 20.3:
Acid and Base Properties of Amines / 20.4:
Reactions of Amines / 20.5:
Syntheses of Amines / 20.6:
Alkaloids / 20.7:
Synthesis of Quinine / 20.8:
Phase-Transfer Catalysis: Ammonium Ions in Synthesis / 20.9:
Aromatic Transition States: Orbital Symmetry / 20.10:
Concerted Reactions / 21.1:
Electrocyclic Reactions / 21.2:
Cycloaddition Reactions / 21.3:
Sigmatropic Shift Reactions / 21.4:
Sigmatropic Shifts of Carbon / 21.5:
Other Sigmatropic Shifts / 21.6:
A Biological Cope Rearrangement / 21.7:
A Molecule with a Fluxional Structure / 21.8:
Introduction to Polyfunctional Compounds: Intramolecular Reactions and Neighboring Group Participation / 21.9:
Heteroatoms as Neighboring Groups / 22.1:
Neighboring [pi] Systems / 22.2:
Single Bonds as Neighboring Groups / 22.3:
Coates' Cation / 22.4:
A Family of Concerted Rearrangements of Acyl Compounds / 22.5:
Polyfunctional Natural Products: Carbohydrates / 22.6:
Nomenclature and Structure / 23.1:
Reactions of Sugars / 23.2:
The Ring Size in Glucose / 23.3:
The Fischer Determination of the Structure of D-Glucose (and the 15 Other Aldohexoses) / 23.4:
An Introduction to Di- and Polysaccharides / 23.5:
Introduction to the Chemistry of Heterocyclic Molecules / 23.6:
Three-Membered Heterocycles: Oxiranes (Epoxides), Thiiranes (Episulfides), and Aziridines / 24.1:
Four-Membered Heterocycles: Oxetanes, Thietanes, and Azetidines / 24.2:
Five- and Six-Membered Heterocycles / 24.3:
Nonaromatic Heterocycles Containing More Than One Heteroatom / 24.4:
Nitrogen-Containing Aromatic Heterocyclic Compounds / 24.5:
Other Aromatic Heterocycles: Furan and Thiophene / 24.6:
Aromatic Heterocycles Containing More Than One Heteroatom / 24.7:
Two-Ring Heterocycles / 24.8:
Bioactive Heterocycles: Penicillin and Related Antibiotics / 24.9:
Introduction to Amino Acids and Polyamino Acids (Peptides and Proteins) / 24.10:
Amino Acids / 25.1:
Reactions of Amino Acids / 25.2:
Peptide Chemistry / 25.3:
Nucleosides, Nucleotides, and Nucleic Acids / 25.4:
Key Terms / 25.5:
Some Commonly Used Abbreviations
Index
Preface
Introduction
Atoms and Molecules; Orbitals and Bonding / Chapter 1.:
11.

図書

図書
by Fritz Feigl in collaboration with Vinzenz Anger ; translated by Ralph E. Oesper
出版情報: Amsterdam ; New York : Elsevier Pub. Co., 1966  xxiii, 772 p. ; 23 cm
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12.

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図書
Stuart J. Baum
出版情報: New York : Macmillan , London : Collier Macmillan, c1987  xv, 526 p. ; 25 cm
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13.

図書

図書
Tse Lok Ho
出版情報: New York : Academic Press, 1977  xii, 209 p. ; 24 cm
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14.

図書

図書
Francis A. Carey and Richard J. Sundberg
出版情報: New York : Plenum Press, c1977  2 v. ; 26 cm
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目次情報:
pt. A. Structure and mechanisms
pt. B. Reactions and synthesis
pt. A. Structure and mechanisms
pt. B. Reactions and synthesis
15.

図書

図書
Edited by Manuel M. Baizer
出版情報: New York : M. Dekker, 1973  xviii, 1072 p ; 24 cm
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16.

図書

図書
Editor : John B. Birks
出版情報: London ; New York : J. Wiley, c1973-c1975  2 v. ; 24 cm
シリーズ名: Wiley monographs in chemical physics
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17.

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図書
edited by G.R. Desiraju
出版情報: Amsterdam ; Tokyo : Elsevier Science, 1987  xx, 550 p. ; 25 cm
シリーズ名: Studies in organic chemistry ; 32
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18.

図書

図書
Ronald Breslow
出版情報: New York : W. A. Benjamin, 1965  xii, 232 p. ; 22 cm
シリーズ名: The Organic chemistry monograph series
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19.

図書

図書
J. L. Malleron, J. C. Fiaud and J. Y. Legros
出版情報: London : Academic, c1997  304 p. ; 30 cm
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Abbreviations
Introduction
Graphical Abstracts of Reaction Numbers (RXN)
Reactions Catalyzed by Palladium Complexes: Cross-Coupling of Organometallics with RX Derivatives
Cross-Coupling of Organometallicswith RCOX Derivatives
Cross-Coupling of Siloxycyclopropanes with RX and RCOX Derivatives
Cross-Coupling of Terminal Alkynes with RX Derivatives
Intermolecular HECK Reaction
Intramolecular HECK Reaction
Intramolecular Coupling of Di(Vinyl Halides)
Tandem HECK-Anion Capture Process of Alkenes, Alkyenes, Alkynes, Allenes and Dienes
Tandem HECK-Anion Capture Process of Norbonene and Related Compounds
Tandem Arylsulfonation-Cyclization Process
Tandem Cyclization-Anion Capture (-Carbonylation) Processof Alkenes and Alkynes
Tandem Cyclization-Anion Capture (-Carbonylation) Process of Ene-Vinyl, Ene-Aryl, and Ene-Alkyl Halides
Tandem Cyclization-Anion Capture Process of Yne-Vinyl and Yne-Aryl Halides
Hydroarylation and Hydrovinylation of Alkenes andAlkynes
Reduction of Alkenes
Semihydrogenation of Alkynes and 1,3-Dienes
Hydroboration, Hydrogennyladon, Hydrosilylation and Hydrostannation of Alkynes, Allenes, Dienes, and Enynes
Hydroselenation of Alkynes
1,4-Disilyation of Conjugated Enones
Hydrocarboxylation, Hydrocarboalkoxylation and Hydrocarboamination of Alkenes and Alkynes
Tandem Carbonylation-Arylation with Alkynes
1,2-Dimetallation of Alkynes and Alkenes and Related Reactions
1,2-Dimetallation of Isonitriles
1,2-Dimetallation of Allenes
Coupling of Aryl Derivatives with Alkenes Involving a Pd(II) Catalyst
Homocoupling of Aryl and Vinyl Derivatives
Codimerization of Alkynes
Codimerization of Terminal Alkynes with Allenes
Codimerization of Alkynes and Allyl Halides
Cyclopropanation of Alkenes and 1,3-Dienes by Diazomethane
Rearrangement of (-Hydroxy Diazo Compounds
Substitution, Addition, and Elimination on Pro-(-Allyl Substrates
[3,3]-Sigmatropic Rearrangement and [1,3]-Shift on Allylic Derivatives
1,3-Diene Monoepoxide Rearrangement
Ring Extension of Cyclobutane Derivatives
[3+2], [3+4], [3+6], [1+2] Cycloadditions
Intramolecular Ene-Like Reactions
Cyclization of Hexatrienolate Derivatives
Amination or Amidation of Alkenes
Alkoxylation of Alkenes and Alkynes
Acetalization of Alkenes
Allylic Acyloxylation of Cycloalkenes
Tandem Acyloxylation-Cyclization of 1,5-Dienes
Tandem Acycloxychlorination-Cyclization of 1,6-Dienes
1,4-Acycloxychlorination of 1,3-Dienes
1,4-Diacyloxylation of 1,3-Dienes and Related Reactions
Intramolecular Amination, Alkoxylation of Acyloxylation of Alkynes
Tandem Intramolecular Amination, Alkoxylation, or Acyloxylation-Allylation of Alkynes and Allenes
Tandem Intramolecular Amination, Alkoxylation, or Acyloxylation-Carbonylation of Alkynes
Intramolecular Amination or Alkoxylation of Alkenes
Tandem Intramolecular Amination or Alkoxylation-Carbonylation of Alkenes and Allenes
Reductive Cyclization with Diynes and Enynes
Cycloisomerization of Diynes and Enynes
Cycloaddition of Aziridines with Carbodiimides
Telomerization of 1,3-Dienes with Nucleophiles
WACKER Process
Preparation of Ketones from Alcohols or Derivatives via a (-Hydride Elimination
Preparation of ((-Unsaturated Carbonyl Derivatives via a (-Hydride Elimination
Preparation of (-Diketones Derivatives via an Oxidative Rearrangement of a Propargyl Acetate
Carbonylation
Isomerization of Alkynes
Addition of Thiols to Alkynes
Preparation of Allylic Acetates from Alkynes by Tandem Redox-Addition
Tandem Cyclization-Capture Process of Enynes
Aldol-Like Condensation of Enol Esters with Aldehydes
Addition of Fluoroalkyl Iodides to Alkenes or Alkynes via a Pd(I) Species
Intermolecular Tandem Carbonylation-Coupling-Cyclization Process of Aryl Halides with Terminal Alkynes.Intramolecular Coupling of Aryl Halides with Arenes
Tandem Intramolecular Alkoxylation-Vinylation of Alkenes
Carbonylative [2+2] Cycloaddition
Dicarboalkoxylation of Alkenes
Addition of Pronucleophile
Abbreviations
Introduction
Graphical Abstracts of Reaction Numbers (RXN)
20.

図書

図書
Philip S. Bailey, Jr., and Christina A. Bailey
出版情報: Boston : Allyn and Bacon, c1981  xvi, 429 p. ; 24 cm
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図書

図書
John McMurry
出版情報: Pacific Grove, Calif. : Brooks/Cole Pub. Co., c1994  xx, 536, 16 p. ; 25 cm
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目次情報: 続きを見る
Preface
A Note for Students
Structure and Bonding; Acids and Bases / 1:
Atomic Structure / 1.1:
Electron Configuration of Atoms / 1.2:
Development of Chemical Bonding Theory / 1.3:
The Nature of Chemical Bonds / 1.4:
Forming Covalent Bonds: Valence Bond Theory / 1.5:
Hybridization: sp[superscript 3] Orbitals and the Structure of Methane / 1.6:
Hybridization: sp[superscript 3] Orbitals and the Structure of Ethane / 1.7:
Hybridization: sp[subscript 2] Orbitals and the Structure of Ethylene / 1.8:
Hybridization: sp Orbitals and the Structure of Acetylene / 1.9:
Polar Covalent Bonds: Electronegativity / 1.10:
Acids and Bases: The Bronsted--Lowry Definition / 1.11:
Acids and Bases: The Lewis Definition / 1.12:
The Nature of Organic Compounds: Alkanes / 2:
Functional Groups / 2.1:
Alkanes and Alkyl Groups: Isomers / 2.2:
Naming Branched-Chain Alkanes / 2.3:
Properties of Alkanes / 2.4:
Conformations of Ethane / 2.5:
Drawing Chemical Structures / 2.6:
Cycloalkanes / 2.7:
Cis--Trans Isomerism in Cycloalkanes / 2.8:
Conformations of Some Cycloalkanes / 2.9:
Axial and Equatorial Bonds in Cyclohexane / 2.10:
Conformational Mobility of Cyclohexane / 2.11:
The Nature of Organic Reactions: Alkenes / 3:
Naming Alkenes / 3.1:
Electronic Structure of Alkenes / 3.2:
Cis--Trans Isomers of Alkenes / 3.3:
Sequence Rules: The E,Z Designation / 3.4:
Kinds of Organic Reactions / 3.5:
How Reactions Occur: Mechanisms / 3.6:
The Mechanism of an Organic Reaction: Addition of HCl to Ethylene / 3.7:
Describing a Reaction: Reaction Energy Diagrams and Transition States / 3.8:
Describing a Reaction: Intermediates / 3.9:
Reactions of Alkenes and Alkynes / 4:
Addition of HX to Alkenes: Hydrohalogenation / 4.1:
Orientation of Alkene Addition Reactions: Markovnikov's Rule / 4.2:
Carbocation Structure and Stability / 4.3:
Addition of H[subscript 2]O to Alkenes: Hydration / 4.4:
Addition of X[subscript 2] to Alkenes: Halogenation / 4.5:
Addition of H[subscript 2] to Alkenes: Hydrogenation / 4.6:
Oxidation of Alkenes: Hydroxylation and Cleavage / 4.7:
Biological Addition Reactions of Alkenes / 4.8:
Addition of Radicals to Alkenes: Polymers / 4.9:
Conjugated Dienes / 4.10:
Stability of Allylic Carbocations: Resonance / 4.11:
Drawing and Interpreting Resonance Forms / 4.12:
Alkynes and Their Reactions / 4.13:
Aromatic Compounds / 5:
Structure of Benzene: The Kekule Proposal / 5.1:
Structure of Benzene: The Resonance Proposal / 5.2:
Naming Aromatic Compounds / 5.3:
Electrophilic Aromatic Substitution Reactions: Bromination / 5.4:
Other Electrophilic Aromatic Substitution Reactions / 5.5:
The Friedel--Crafts Alkylation and Acylation Reactions / 5.6:
Substituent Effects in Electrophilic Aromatic Substitution / 5.7:
An Explanation of Substituent Effects / 5.8:
Oxidation and Reduction of Aromatic Compounds / 5.9:
Polycyclic Aromatic Hydrocarbons / 5.10:
Organic Synthesis / 5.11:
Stereochemistry / 6:
Stereochemistry and the Tetrahedral Carbon / 6.1:
The Reason for Handedness in Molecules: Chirality / 6.2:
Optical Activity / 6.3:
Specific Rotation / 6.4:
Pasteur's Discovery of Enantiomers / 6.5:
Sequence Rules for Specifying Configuration / 6.6:
Diastereomers / 6.7:
Meso Compounds / 6.8:
Molecules with More Than Two Stereocenters / 6.9:
Racemic Mixtures and the Resolution of Enantiomers / 6.10:
Physical Properties of Stereoisomers / 6.11:
A Brief Review of Isomerism / 6.12:
Chirality in Nature / 6.13:
Alkyl Halides / 7:
Naming Alkyl Halides / 7.1:
Preparing Alkyl Halides / 7.2:
Reactions of Alkyl Halides: Grignard Reagents / 7.3:
Nucleophilic Substitution Reactions / 7.4:
The S[subscript N]2 Reaction / 7.5:
The S[subscript N]1 Reaction / 7.6:
Eliminations: The E2 Reaction / 7.7:
Eliminations: The E1 Reaction / 7.8:
A Summary of Reactivity: S[subscript N]1, S[subscript N]2, E1, E2 / 7.9:
Substitution Reactions in Living Organisms / 7.10:
Alcohols, Phenols, and Ethers / 8:
Naming Alcohols, Phenols, and Ethers / 8.1:
Properties of Alcohols, Phenols, and Ethers: Hydrogen Bonding / 8.2:
Properties of Alcohols and Phenols: Acidity / 8.3:
Synthesis of Alcohols / 8.4:
Reactions of Alcohols / 8.5:
Synthesis and Reactions of Phenols / 8.6:
Synthesis and Reactions of Ethers / 8.7:
Cyclic Ethers: Epoxides / 8.8:
Thiols and Sulfides / 8.9:
Aldehydes and Ketones: Nucleophilic Addition Reactions / 9:
The Nature of Carbonyl Compounds / 9.1:
Naming Aldehydes and Ketones / 9.2:
Synthesis of Aldehydes and Ketones / 9.3:
Oxidation of Aldehydes / 9.4:
Nucleophilic Addition Reactions of Aldehydes and Ketones: Reduction / 9.5:
Nucleophilic Addition of Water: Hydration / 9.6:
Nucleophilic Addition of Alcohols: Acetal Formation / 9.7:
Nucleophilic Addition of Amines: Imine Formation / 9.8:
Nucleophilic Addition of Grignard Reagents: Alcohol Formation / 9.9:
Conjugate Nucleophilic Addition Reactions / 9.10:
Some Biological Nucleophilic Addition Reactions / 9.11:
Carboxylic Acids and Derivatives / 10:
Naming Carboxylic Acids and Derivatives / 10.1:
Occurrence and Properties of Carboxylic Acids / 10.2:
Synthesis of Carboxylic Acids / 10.3:
Nucleophilic Acyl Substitution Reactions / 10.4:
Reactions of Carboxylic Acids / 10.5:
Chemistry of Acid Halides / 10.6:
Chemistry of Acid Anhydrides / 10.7:
Chemistry of Esters / 10.8:
Chemistry of Amides / 10.9:
Chemistry of Nitriles / 10.10:
Polymers from Carbonyl Compounds: Nylons and Polyesters / 10.11:
Carbonyl Alpha-Substitution Reactions and Condensation Reactions / 11:
Keto--Enol Tautomerism / 11.1:
Reactivity of Enols: The Mechanism of Alpha-Substitution Reactions / 11.2:
Alpha Halogenation of Aldehydes and Ketones / 11.3:
Acidity of Alpha Hydrogen Atoms: Enolate Ion Formation / 11.4:
Reactivity of Enolate Ions / 11.5:
Alkylation of Enolate Ions / 11.6:
Carbonyl Condensation Reactions / 11.7:
Condensations of Aldehydes and Ketones: The Aldol Reaction / 11.8:
Dehydration of Aldol Products: Synthesis of Enones / 11.9:
Condensations of Esters: The Claisen Condensation Reaction / 11.10:
Biological Carbonyl Reactions / 11.11:
Amines / 12:
Naming Amines / 12.1:
Structure and Properties of Amines / 12.2:
Basicity of Amines / 12.3:
Synthesis of Amines / 12.4:
Reactions of Amines / 12.5:
Heterocyclic Amines / 12.6:
Alkaloids: Naturally Occurring Amines / 12.7:
Structure Determination / 13:
Infrared Spectroscopy and the Electromagnetic Spectrum / 13.1:
Infrared Spectroscopy of Organic Molecules / 13.2:
Ultraviolet Spectroscopy / 13.3:
Interpreting Ultraviolet Spectra: The Effect of Conjugation / 13.4:
Nuclear Magnetic Resonance Spectroscopy / 13.5:
The Nature of NMR Absorptions / 13.6:
Chemical Shifts / 13.7:
Chemical Shifts in [superscript 1]H NMR Spectra / 13.8:
Integration of [superscript 1]H NMR Spectra: Proton Counting / 13.9:
Spin--Spin Splitting in [superscript 1]H NMR Spectra / 13.10:
Uses of [superscript 1]H NMR Spectra / 13.11:
[superscript 13]C NMR Spectroscopy / 13.12:
Biomolecules: Carbohydrates / 14:
Classification of Carbohydrates / 14.1:
Configurations of Monosaccharides: Fischer Projections / 14.2:
D,L Sugars / 14.3:
Configurations of Aldoses / 14.4:
Cyclic Structures of Monosaccharides: Hemiacetal Formation / 14.5:
Monosaccharide Anomers: Mutarotation / 14.6:
Reactions of Monosaccharides / 14.7:
Polysaccharides / 14.9:
Other Important Carbohydrates / 14.10:
Cell-Surface Carbohydrates and Carbohydrate Vaccines / 14.11:
Biomolecules: Amino Acids, Peptides, and Proteins / 15:
Structures of Amino Acids / 15.1:
Isoelectric Points / 15.2:
Peptides and Proteins / 15.3:
Covalent Bonding in Peptides / 15.4:
Peptide Structure Determination: Amino Acid Analysis / 15.5:
Peptide Sequencing: The Edman Degradation / 15.6:
Peptide Synthesis / 15.7:
Classification of Proteins / 15.8:
Protein Structure / 15.9:
Enzymes / 15.10:
How Do Enzymes Work? Citrate Synthase / 15.11:
Biomolecules: Lipids and Nucleic Acids / 16:
Lipids / 16.1:
Fats and Oils / 16.2:
Soaps / 16.3:
Phospholipids / 16.4:
Steroids / 16.5:
Nucleic Acids and Nucleotides / 16.6:
Structure of DNA / 16.7:
Base Pairing in DNA: The Watson--Crick Model / 16.8:
Nucleic Acids and Heredity / 16.9:
Replication of DNA / 16.10:
Structure and Synthesis of RNA: Transcription / 16.11:
RNA and Protein Biosynthesis: Translation / 16.12:
Sequencing DNA / 16.13:
The Polymerase Chain Reaction / 16.14:
The Organic Chemistry of Metabolic Pathways / 17:
An Overview of Metabolism and Biochemical Energy / 17.1:
Catabolism of Fats: [beta]-Oxidation Pathway / 17.2:
Catabolism of Carbohydrates: Glycolysis / 17.3:
The Citric Acid Cycle / 17.4:
Catabolism of Proteins: Transamination / 17.5:
The Organic Chemistry of Metabolic Pathways: A Summary / 17.6:
Appendixes
Nomenclature of Polyfunctional Organic Compounds / A:
Glossary / B:
Answers to Selected In-Chapter Problems / C:
Index
Preface
A Note for Students
Structure and Bonding; Acids and Bases / 1:
22.

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図書
Robert Thornton Morrison, Robert Neilson Boyd
出版情報: Boston, Mass. : Allyn and Bacon, c1983  xxiv, 1370 p. ; 26 cm
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目次情報: 続きを見る
Structure and Properties / 1:
Methane / 2:
Energy of Activation
Transition State
Alkanes / 3:
Free-Radical Substitution
Stereochemistry I / 4:
Stereoisomers
Alkyl Halides / 5:
Nucleophilic Aliphatic Substitution
Alcohols and Ethers / 6:
Role of the Solvent / 7:
Secondary Bonding
Alkenes I / 8:
Structure and Preparation
Elimination
Alkenes II / 9:
Reactions of the Carbon-Carbon Double Bond
Electrophilic and Free-Radical Addition
Stereochemistry II / 10:
Stereoselective and Stereospecific Reactions
Conjugation and Resonance / 11:
Dienes
Alkynes / 12:
Alicyclic Compounds / 13:
Aromaticity / 14:
Benzene
Electrophilic Aromatic Substitution / 15:
Aromatic-Aliphatic Compounds / 16:
Arenes and Their Derivatives
Spectroscopy and Structure / 17:
Aldehydes and Ketones / 18:
Nucleophilic Addition
Carboxylic Acids / 19:
Functional Derivatives of Carboxylic Acids / 20:
Nucleophilic Acyl Substitution
Carbanions I / 21:
Amines I / 22:
Preparation and Physical Properties
Amines II / 23:
Reactions
Phenols / 24:
Carbanions II / 25:
Aryl Halides / 26:
Nucleophilic Aromatic Substitution
a,B-Unsaturated Carbonyl Compounds / 27:
Conjugate Addition
Molecular Orbitals / 28:
Orbital Symmetry
Symphoria / 29:
Neighboring Group Effects
Catalysis by Transition Metal Complexes
Heterocyclic Compounds / 30:
Macromolecules / 31:
Polymers and Polymerization
Stereochemistry III / 32:
Enantiotopic and Diastereotopic Ligands and Fats
Lipids / 33:
Fats and Steroids
Carbohydrates I / 34:
Monosaccharides
Carbohydrates II / 35:
Disaccharides and Polysaccharides
Proteins and Nucleic Acids / 36:
Molecular Biology
Structure and Properties / 1:
Methane / 2:
Energy of Activation
23.

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図書
by Michinori Ōki
出版情報: Deerfield Beach, FL : VCH Publishers , Weinheim : VCH Verlagsgesellschaft, c1985  xii, 423 p. ; 25 cm
シリーズ名: Methods in stereochemical analysis ; v. 4
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24.

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図書
A. P. Ryles, K. Smith, and R. S. Ward
出版情報: Chichester ; New York : Wiley, c1980  xiv, 306 p. ; 24 cm
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25.

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図書
edited by Shohei Inoue, Noboru Yamazaki
出版情報: Tokyo : Kodansha, 1981  xi, 280 p. ; 24 cm
シリーズ名: Kodansha scientific books
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26.

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図書
Kenneth B. Wiberg
出版情報: New York ; London : Wiley, c1964  viii, 591 p. ; 24 cm
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27.

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図書
Penny A. Chaloner
出版情報: London ; Boston : Butterworths, 1986  1002 p. ; 24 cm
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28.

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図書
M. Schnitzer, S. U. Khan
出版情報: Ann Arbor, Mich. : University Microfilms International, 1972  vii, 327 p. ; 24 cm
シリーズ名: Books in soils and the environment
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29.

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図書
Bruno Jirgensons
出版情報: Oxford ; New York : Pergamon Press, 1962  x, 464 p. ; 24 cm
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30.

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図書
Marye Anne Fox, James K. Whitesell
出版情報: Boston : Jones and Bartlett, c1994  xxvi, 870 p. ; 29 cm
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目次情報: 続きを見る
Structure and Bonding in Alkanes / 1:
Alkenes, Aromatic Hydrocarbons, and Alkynes / 2:
Functional Groups Containing Heteroatoms / 3:
Chromatography and Spectroscopy / 4:
Stereochemistry / 5:
Understanding Organic Reactions / 6:
Mechanisms of Organic Reactions / 7:
Substitution by Nucleophiles at sp3-Hybridized Carbon / 8:
Elimination Reactions / 9:
Addition to Carbon-Carbon Multiple Bonds / 10:
Electrophilic Aromatic Substitution / 11:
Nucleophilic Addition and Substitution at Carbonyl Groups / 12:
Substitution Alpha to Carbonyl Groups / 13:
Skeletal-Rearrangement Reactions / 14:
Multistep Syntheses / 15:
Polymeric Materials / 16:
Naturally Occurring Oxygen-Containing Compounds / 17:
Naturally Occurring Nitrogen-Containing Compounds / 18:
Noncovalent Reactions and Molecular Recognition / 19:
Catalyzed Reactions / 20:
Cofactors for Biological Redox Reactions / 21:
Energy Storage in Organic Molecules / 22:
Molecular Basis for Drug Action / 23:
Structure and Bonding in Alkanes / 1:
Alkenes, Aromatic Hydrocarbons, and Alkynes / 2:
Functional Groups Containing Heteroatoms / 3:
31.

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図書
Lawrence J. Andrews and Raymond M. Keefer
出版情報: Amsterdam : Holden-Day, 1964.  196 p. ; 25 cm.
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32.

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図書
by S.C. Nyburg
出版情報: New York : Academic Press, 1961  xii, 434 p. ; 24 cm
シリーズ名: Organic and biological chemistry : a series of monographs ; 4
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33.

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図書
John G. Burr
出版情報: New York : Interscience Publishers, 1957  291 p. ; 24 cm
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34.

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図書
by Helmut Krauch and Werner Kunz ; with a foreword by Friedrich Richter ; translated from the 2d rev. German ed. (with addendum) by John M. Harkin
出版情報: New York : Wiley, 1964, c1962  xxiii, 620 p ; 24 cm
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35.

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図書
[by] John D. Roberts [and] Marjorie C. Caserio
出版情報: New York : W.A. Benjamin, c1967  2 v.(xxi, 844 p., vii, 513 p.) ; 23-26 cm
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36.

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図書
edited by L. M. Jackman
出版情報: London ; Boston : Butterworths, 1976  172 p. ; 25 cm
シリーズ名: International review of science ; . Organic chemistry ; Ser. 2 ; v. 1
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37.

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図書
Christian Reichardt
出版情報: Weinheim, Federal Republic of Germany ; New York, NY, USA : VCH, c1988  xxii, 534 p. ; 25 cm
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目次情報: 続きを見る
Introduction
Solute-Solvent Interactions
Classification of Solvents
Solvent Effects on the Position of Homogeneous Chemical Equilibria
Solvent Effects on the Rate of Homogeneous Chemical Reactions
Solvent Effects on Absorption Spectra of Organic Compounds
Empirical Parameters of Solvent Polarity
Appendix
References
Introduction
Solute-Solvent Interactions
Classification of Solvents
38.

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図書
Edwin S. Gould
出版情報: New York : Holt, c1959  790 p ; 25 cm
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39.

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図書
Roger A. Sheldon, Jay K. Kochi
出版情報: New York : Academic Press, 1981  xxi, 424 p. ; 24 cm
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40.

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図書
[by] Donald J. Cram [and] George S. Hammond
出版情報: New York : McGraw-Hill, [c1964]  x, 846 p. ; 24 cm
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41.

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図書
John C. Stowell
出版情報: New York : John Wiley & Sons, c1988  xv, 268 p. ; 24 cm
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目次情報: 続きを見る
Reading Nomenclature
Searching the Literature
Stereochemistry
Functional Group Transformations
Carbon-Carbon Bond Formation
Planning Multistep Syntheses
Mechanisms and Predictions
Electron Delocalization, Aromatic Character, and Pericyclic Reactions
Physical Influences on Reactions
Interpretation of NMR Spectra
Index
Reading Nomenclature
Searching the Literature
Stereochemistry
42.

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図書
E.A. Silinsh
出版情報: Berlin ; New York : Springer-Verlag, 1980  xvii, 389 p. ; 24 cm
シリーズ名: Springer series in solid-state sciences ; v. 16
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43.

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図書
edited by Kenneth B. Wiberg
出版情報: New York ; London ; Tokyo : Academic Press, 1965-1982  4 v. ; 24 cm
シリーズ名: Organic chemistry : a series of monographs ; v. 5
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44.

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図書
M. Pesez and J. Bartos
出版情報: New York : M. Dekker, c1974  xiv, 672 p. ; 24 cm
シリーズ名: Clinical and biochemical analysis ; v. 1
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45.

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図書
William J. le Noble
出版情報: New York : M. Dekker, 1974  xvii, 976 p. ; 25 cm
シリーズ名: Studies in Organic Chemistry ; v. 3
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46.

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Douglas C. Neckers, Michael P. Doyle
出版情報: New York : Wiley, c1977  xxxvi, 1147 p. ; 26 cm
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47.

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図書
by M.R. Rifi and Frank H. Covitz
出版情報: New York : M. Dekker, 1974  viii, 417 p. ; 24 cm
シリーズ名: Techniques and applications in organic synthesis
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48.

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図書
[edited by] Michael Szwarc
出版情報: New York : Wiley-Interscience, [1972-74]  2 v ; 23 cm
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49.

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Michael J. S. Dewar and Ralph C. Dougherty
出版情報: New York : Plenum Press, c1975  xiii, 576 p. ; 23 cm
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50.

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図書
[by] Michael J.S. Dewar
出版情報: New York : McGraw-Hill, c1969  xiv, 484 p. ; 23 cm
シリーズ名: McGraw-Hill series in advanced chemistry
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51.

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図書
Ernest L. Eliel
出版情報: New York : McGraw-Hill , Tokyo : Kōgakusha, c1962  xv, 486 p. ; 21 cm
シリーズ名: McGraw-Hill series in advanced chemistry
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52.

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Alan H. Haines
出版情報: London : Academic, 1988  xx, 467 p ; 24 cm
シリーズ名: Best synthetic methods
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53.

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図書
[by] R. Foster
出版情報: London ; New York : Academic Press, 1969  xii, 470 p. ; 24 cm
シリーズ名: Organic chemistry : a series of monographs ; v. 15
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54.

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図書
edited by Manuel M. Baizer, Henning Lund
出版情報: New York : M. Dekker, c1983  xviii, 1166 p. ; 27 cm
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55.

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図書
edited by C. H. Bamford and C. F. H. Tipper
出版情報: Amsterdam ; New York : Elsevier Pub. Co., 1972  xv, 615 p. ; 25 cm
シリーズ名: Comprehensive chemical kinetics ; v. 7
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56.

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図書
by H. L. Heys ; with a foreword by E. D. Hughes
出版情報: London : Harrap, 1960  236 p ; 23 cm
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57.

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図書
by Petr Zuman
出版情報: Oxford : Pergamon Press , [Distributed in the Western Hemisphere by Macmillan], 1964  x, 313 p. ; 23 cm
シリーズ名: International series of monographs on analytical chemistry / General editors, R. Belcher and L. Gordon ; v. 12
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58.

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図書
edited by C.H. Bamford and C.F.H. Tipper
出版情報: Amsterdam ; New York : Elsevier Pub. Co., 1972  xvi, 779 p. ; 25 cm
シリーズ名: Comprehensive chemical kinetics ; v. 5
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59.

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図書
Archibald J. Baker ... [et al.]
出版情報: London : Heyden, c1967  25, 60 p. ; 28 cm
シリーズ名: Spectroscopy in education series ; v. 4
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60.

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図書
edited by Saul Patai
出版情報: London : Wiley, 1977  2 v. (xv, 1343 p) ; 24 cm
シリーズ名: The Chemistry of functional groups ; supplement A; 6-1,2
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61.

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John Griffiths
出版情報: London ; New York : Academic Press, 1976  ix, 281 p. ; 24 cm
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62.

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by Bruno Jirgensons
出版情報: Amsterdam : Elsevier, 1958  xiv, 655 p. ; 24 cm
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63.

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図書
by L. M. Jackman and S. Sternhell
出版情報: Oxford ; New York : Pergamon Press, [1969]  xvi, 456 p. ; 27 cm
シリーズ名: International series of monographs on organic chemistry ; v. 5
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64.

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図書
George C. Levy, Robert L. Lichter
出版情報: New York : Wiley, c1979  ix, 221 p. ; 24 cm
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65.

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図書
ed by Sidney Siggia
出版情報: New York : Wiley, 1963  697 p. ; 24 cm
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66.

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図書
Alsoph H. Corwin, Maurice M. Bursey
出版情報: London : Addison-Wesley, 1966  xviii, 746 p. ; 22 cm
シリーズ名: Addison-Wesley world student series
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67.

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J.H. Beynon
出版情報: Amsterdam ; New York : Elsevier, 1960  xii, 640 p. ; 25 cm
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68.

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図書
edited by P. Zuman
出版情報: London : Plenum Publishing Co., 1970  ix, 530 p. ; 25 cm
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69.

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図書
Lionel Salem
出版情報: Reading, Mass. : W.A. Benjamin, 1966  xvi, 576 p. ; 24 cm
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70.

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図書
Petr Zuman, With foreword by J. Heyrovsky
出版情報: New York : Plenum Press, 1967  xvi, 384 p. ; 24 cm
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71.

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図書
[by] C. David Gutsche [and] Daniel J. Pasto
出版情報: Englewood Cliffs, N.J. : Prentice-Hall, [1975]  viii, 1240 p. ; 25 cm
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72.

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図書
by Fritz Feigl ; translated by Ralph E. Oesper
出版情報: Amsterdam ; New York : Elsevier Pub. Co , Tokyo : Maruzen, 1961  675 p. ; 22 cm
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73.

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図書
Miloš Hudlický
出版情報: Washington, DC : American Chemical Society, 1990  xx, 433 p. ; 24 cm
シリーズ名: ACS monograph ; no. 186
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目次情報: 続きを見る
Oxidation Agents
Dehydrogenations
Oxidations
Preparative Procedures
Oxidation Agents
Dehydrogenations
Oxidations
74.

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図書
Wolfgang J. Kirsten
出版情報: New York : Academic Press, 1983  xii, 146 p. ; 24 cm
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75.

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図書
Alexander McKillop
出版情報: New York : Pergamon, 1997  xix, 153 p. ; 25 cm
シリーズ名: Tetrahedron organic chemistry series ; v. 16
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Selected Problems: A tandem route to 1,2,3,4-tetrasubstituted naphthalenes
The Hooker oxidation
Benzopyrene synthesis - by accident
Lactone ammonolysis
Acid-catalysed condensation of indole with acetone
Flash vacuum pyrolysis of o-xylylene dimers
A ""stable enol"" that doesn't exist
Reaction of benzothiazole with DMAD
Ring contractions of a dibenzothiepinone
Rearrangement of 6-hydroxyprotopine to dihydrosanguinarine
An intramolecular Wittig reaction
Easy contruction of a tricyclic indole related to
Selected Problems: A tandem route to 1,2,3,4-tetrasubstituted naphthalenes
The Hooker oxidation
Benzopyrene synthesis - by accident
76.

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図書
T. W. Graham Solomons, Craig B. Fryhle, Scott A. Snyder
出版情報: Hoboken, N.J. : John Wiley & Sons, c2016  xxviii, 1124, 8, 22, 23 p. ; 28 cm
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77.

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Leroy G. Wade, Jr. ; contributing author, Jan William Simek
出版情報: Harlow : Pearson, c2017  1394 p. ; 28 cm
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78.

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Frederick A. Bettelheim ... [et al.]
出版情報: Boston, MA : Cengage Learning, c2016  1 v. (various pagings) ; 29 cm
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79.

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William H. Brown, Thomas Poon
出版情報: Hoboken, N.J. : Wiley, c2014  xxiv, 673, 4, 9, 11 p. ; 28 cm
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80.

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図書
A. I. Kitaigorodskii
出版情報: New York : Consultants Bureau, c1961  x, 541 p. ; 26 cm
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81.

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図書
Bernard Miller
出版情報: Upper Saddle River, N.J. : Prentice Hall, 2004  xvi, 411 p. ; 25 cm
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目次情報: 続きを見る
Introduction / 1:
Mechanisms of Reactions. Electron Delocalization and Resonance
Electrocyclic Reactions / 2:
Conrotatory and Disrotatory Processes
Explanations for the Woodward-Hoffman Rules
Electrocyclic Reactions with Odd Numbers of Atoms
Photochemical Cyclizations
Cycloaddiction and Cycloreversion Reactions / 3:
Suprafacial and Antarafacial Addition
Selection Rules for Cycloaddition and Cycloreversion Reactions
Examples of Thermal Cycloaddition Reactions
Photochemical Cycloadditions
Sigmatropic Reactions / 4:
Theory of Sigmatropic Shifts
Experimental Observations
Sigmatropic Rearrangements of Charged Systems
Linear Free-Energy Relationships / 5:
The Hammett Equation
Separation of Polar, Resonance, and Steric Effects
Migrations to Electron-Deficient Centers / 6:
Migrations to Electron-Deficient Carbons
The Nature of the Migrating Groups
Rearrangements of Carbocations. Long-Distance Migrations
Migrations to Nitrogen and Oxygen
Neighboring-Group Effects and Nonclassical Cations / 7:
Substitution with Retention of Configuration
Cyclic Halonium Ions
Sulfur and Nitrogen Mustards
Trans/Cis Rate Ratios. Neighboring Acetoxy Groups
Cyclic Phenonium Ions. Double Bonds as Neighboring Groups
Cyclopropane Rings as Neighboring Groups
Neighboring Alkyl Groups: 2-Norbornyl Cations
Rearrangements of Carbanions and Free Radicals / 8:
Carbanion Rearrangements
Rearrangements of Free Radicals
Carbenes, Carbenoids, and Nitrenes / 9:
Formation of Carbenes and Nitrenes
Singlet and Triplet Carbenes. Additions to Double Bonds
Insertion Reactions. Rearrangements
Six-Membered Heterocyclic Rings / 10:
Aromatic Heterocyclic Molecules
Reactions of Pyridine and Its Analogs
Synthesis of Six-Membered Heterocyclic Rings
Five-Membered Heterocyclic Rings / 11:
Electron Delocalization and Aromaticity
Reactions of Five-Membered Heterocyclic Rings
Synthesis of Five-Membered Heteroaromatic Rings
Index
Introduction / 1:
Mechanisms of Reactions. Electron Delocalization and Resonance
Electrocyclic Reactions / 2:
82.

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図書
Toshio Fuchigami and Shinsuke Inagi, Mahito Atobe
出版情報: Chichester, West Sussex : Wiley, 2015  xii, 226 p. ; 24 cm
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83.

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図書
出版情報: London : Chemical Society, c1968-  v. ; 23 cm
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84.

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図書
Klaus Weissermel, Hans-Jürgen Arpe
出版情報: Weinheim : Wiley-VCH, 2003  xix, 491 p. ; 25 cm
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Various Aspects of Energy and Raw Material Supply / 1:
Basic Products of Industrial Syntheses / 2:
Olefins / 3:
Acetylene / 4:
1,3-Diolefins / 5:
Syntheses Involving Carbon Monoxide / 6:
Oxidation Products of Ethylene / 7:
Alcohols / 8:
Vinyl-Halogen and Vinyl-Oxygen Compounds / 9:
Components for Polyamides / 10:
Propene Conversion Products / 11:
Aromatics - Production and Conversion / 12:
Benzene Derivatives / 13:
Oxidation Products of Xylene and Naphthalene / 14:
Appendix / 15:
Index
Various Aspects of Energy and Raw Material Supply / 1:
Basic Products of Industrial Syntheses / 2:
Olefins / 3:
85.

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図書
edited by C.H. Bamford and C.F.H. Tipper
出版情報: Amsterdam ; New York : Elsevier Pub. Co., 1972  xv, 517 p. ; 25 cm
シリーズ名: Comprehensive chemical kinetics ; v. 6
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86.

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図書
Neil E. Schore
出版情報: New York : W.H. Freeman, c2007  x, 485 p. ; 28 cm
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87.

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図書
Paula Yurkanis Bruice
出版情報: Upper Saddle River : Pearson Prentice Hall, c2007  xxxviii, 1319, 35, 14, 1, 27 p., plates. [3] p. ; 27 cm
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目次情報: 続きを見る
An Introduction to the Study of Organic Chemistry / Part I:
Electronic Structure and Bonding middot; Acids and Bases / Chapter 1:
The Structure of an Atom / 1.1:
How the Electrons in an Atom are Distributed / 1.2:
Ionic and Covalent Bonds / 1.3:
Ionic Bonds are Formed by the Transfer of Electrons
Covalent Bonds are Formed by Sharing Electrons
Polar Covalent Bonds
How the Structure of a Compound is Represented / 1.4:
Lewis Structures
Kekule Structures
Condensed Structures
Atomic Orbitals / 1.5:
An Introduction to Molecular Orbital Theory / 1.6:
How Single Bonds are Formed in Organic Compounds / 1.7:
The Bonds in Methane
An Introduction to the Study of Organic Chemistry / Part I:
Electronic Structure and Bonding middot; Acids and Bases / Chapter 1:
The Structure of an Atom / 1.1:
88.

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図書
editors: David Fox, Mortimer M. Labes and Arnold Weissberger
出版情報: New York : Interscience Publishers, 1963-1967  3 v. ; 24 cm
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89.

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図書
by W. Mansfield Clark
出版情報: Baltimore : Williams & Wilkins, c1960  xi, 584 p. ; 24 cm
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90.

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図書
Andrew Streitwieser, Jr
出版情報: New York : Wiley, c1961  xvi, 489 p. ; 24 cm
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91.

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図書
Jonathan Clayden, Nick Greeves, Stuart Warren
出版情報: Oxford : Oxford University Press, c2012  xxv, 1234 p. ; 28 cm
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目次情報: 続きを見る
What Is Organic Chemistry? / 1:
Organic Structures / 2:
Determining Organic Structures / 3:
Structure of Molecules / 4:
Organic Reactions / 5:
Nucleophilic Addition to the Carbonyl Group / 6:
Delocalization and Conjugation / 7:
Acidity, Basicity, and Pka / 8:
Using Organometallic Reagents to Make C-C Bonds / 9:
Nucleophilic Substitution at the Carbonyl Group / 10:
Nucleophilic Substitution at C=O with Loss of Carbonyl Oxygen / 11:
Equilibria, Rates, and Mechanisms / 12:
1H NMR: Proton Nuclear Magnetic Resonance / 13:
Stereochemistry / 14:
Nucleophilic Substitution at Saturated Carbon / 15:
Conformational Analysis / 16:
Elimination Reactions / 17:
Review of Spectroscopic Methods / 18:
Electrophilic Addition to Alkenes / 19:
Formation and Reactions of Enols and Enolates / 20:
Electrophilic Aromatic Substitution / 21:
Conjugate Addition and Nucleophilic Aromatic Substitution / 22:
Chemoselectivity and Protecting Groups / 23:
Regioselectivity / 24:
Alkylation of Enolates / 25:
Reactions of Enolates with Carbonyl Compounds: The Aldol and Claisen Reactions / 26:
Sulfur, Silicon, and Phosphorus in Organic Chemistry / 27:
Retrosynthetic Analysis / 28:
Aromatic Heterocycles 1: Structures and Reactions / 29:
Aromatic Heterocycles 2: Synthesis / 30:
Saturated Heterocycles and Stereoelectronics / 31:
Stereoselectivity in Cyclic Molecules / 32:
Diastereoselectivity / 33:
Pericyclic Reactions 1: Cycloadditions / 34:
Pericyclic Reactions 2: Sigmatropic and Electrocyclic Reactions / 35:
Participation, Rearrangement, and Fragmentation / 36:
Radical Reactions / 37:
Synthesis and Reactions of Carbenes / 38:
Determining Reaction Mechanisms / 39:
Organometallic Chemistry / 40:
Asymmetric Synthesis / 41:
Organic Chemistry of Life / 42:
Organic Chemistry Today / 43:
What Is Organic Chemistry? / 1:
Organic Structures / 2:
Determining Organic Structures / 3:
92.

図書

図書
W.A. Waters
出版情報: London : Methuen , New York : Wiley, 1964  152 p. ; 23 cm
シリーズ名: Methuen's monographs on chemical subjects
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