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1.

図書

東工大
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図書
東工大
目次DB
T.W. Graham Solomons, Craig B. Fryhle, Robert G. Johnson [著] ; 池田正澄 [ほか] 監訳
出版情報: 東京 : 廣川書店, 2008.4  vii, 279p ; 26cm
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1. 有機化学の基礎 : 化学結合と分子構造 1
2. 代表的な炭素化合物 13
3. 有機化学反応序論 : 酸と塩基 19
4. アルカンとシクロアルカンの命名法と立体配座 27
5. 立体化学 : キラルな分子 39
6. イオン反応 : ハロゲン化アルキルの求核置換反応と脱離反応 51
7. アルケンとアルキンⅠ : 性質と合成.ハロゲン化アルキルの脱離反応 63
8. アルケンとアルキンⅡ : 付加反応 79
9. ラジカル反応 91
10. アルコール,エーテル,およびチオール 97
11. カルボニル化合物からアルコールの合成 : 酸化還元反応と有機金属化合物 109
12. 共役不飽和系 129
13. 芳香族化合物 141
14. 芳香族化合物の反応 147
15. アルデヒドとケトンⅠ : カルボニル基への求核付加 165
16. アルデヒドとケトンⅡ : エノールとエノラート 181
17. カルボン酸とその誘導体 : アシル炭素上の求核付加-脱離反応 197
18. β-ジカルボニル化合物の合成と反応 : エノラートの化学 213
19. アミン 231
20. フェノールとハロゲン化アリール : 芳香族求核置換反応 255
21. 炭水化物 265
22. 脂質 269
23. アミノ酸とタンパク質 273
24. 核酸とタンパク質合成 277
1. 有機化学の基礎 : 化学結合と分子構造 1
2. 代表的な炭素化合物 13
3. 有機化学反応序論 : 酸と塩基 19
2.

図書

図書
Maitland Jones, Jr. and Henry L. Gingrich
出版情報: New York : Norton , 東京 : 東京化学同人(発売), 2001, c2000  x, 787 p. ; 28 cm
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3.

図書

図書
Susan McMurry
出版情報: 東京 : 東京化学同人 (発売), 2000.4  361p ; 24cm
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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:
4.

図書

図書
T.W. Graham Solomons, Craig B. Fryhle, Robert G. Johnson [著] ; 花房昭静, 池田正澄, 上西潤一監訳
出版情報: 東京 : 廣川書店, 2002.10  vii, 262, 55p ; 26cm
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5.

図書

図書
Reinhard Bruckner
出版情報: San Diego : Hercourt/Academic Press, c2002  xxi, 636 p. ; 24 cm
シリーズ名: Advanced organic chemistry series
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Foreword
Preface to the English Edition
Preface to the German Edition
Acknowledgments
Radical Substitution Reactions at the Saturated C Atom / 1:
Bonding and Preferred Geometries in C Radicals, Carbenium Ions and Carbanions / 1.1:
Stability of Radicals / 1.2:
Relative Rates of Analogous Radical Reactions / 1.3:
Radical Substitution Reactions: Chain Reactions / 1.4:
Radical Initiators / 1.5:
Radical Chemistry of Alkylmercury(II) Hydrides / 1.6:
Radical Halogenation of Hydrocarbons / 1.7:
Autoxidations / 1.8:
Defunctionalizations via Radical Substitution Reactions / 1.9:
References
Nucleophilic Substitution Reactions at the Saturated C Atom / 2:
Nucleophiles and Electrophiles; Leaving Groups / 2.1:
Good and Poor Nucleophiles / 2.2:
Leaving Groups and the Quality of Leaving Groups / 2.3:
S[subscript N]2 Reactions: Kinetic and Stereochemical Analysis--Substituent Effects on Reactivity / 2.4:
S[subscript N]1 Reactions: Kinetic and Stereochemical Analysis; Substituent Effects on Reactivity / 2.5:
When Do S[subscript N] Reactions at Saturated C Atoms Take Place According to the S[subscript N]1 Mechanism and When Do They Take Place According to the S[subscript N]2 Mechanism? / 2.6:
Unimolecular S[subscript N] Reactions That Do Not Take Place via Simple Carbenium Ion Intermediates: Neighboring Group Participation / 2.7:
Preparatively Useful S[subscript N]2 Reactions: Alkylations / 2.8:
Additions to the Olefinic C=C Double Bond / 3:
The Concept of cis and trans Addition / 3.1:
Vocabulary of Stereochemistry and Stereoselective Synthesis I / 3.2:
Additions That Take Place Diastereoselectivity as cis Additions / 3.3:
Enantioselective cis Additions to C=C Double Bonds / 3.4:
Additions That Take Place Diastereoselectively as trans Additions (Additions via Onium Intermediates) / 3.5:
Additions That Take Place or Can Take Place without Stereocontrol Depending on the Mechanism / 3.6:
[beta]-Eliminations / 4:
Concepts of Elimination Reactions / 4.1:
[beta]-Eliminations of H/Het via Cyclic Transition States / 4.2:
[beta]-Eliminations of H/Het via Acyclic Transition States: The Mechanistic Alternatives / 4.3:
E2 Eliminations of H/Het and the E2/S[subscript N]2 Competition / 4.4:
E1 Elimination of H/Het from R[subscript tert]--X and the E1/S[subscript N]1 Competition / 4.5:
E1[subscript cb] Eliminations / 4.6:
[beta]-Eliminations of Het[superscript 1]/Het[superscript 2] / 4.7:
Substitution Reactions on Aromatic Compounds / 5:
Electrophilic Aromatic Substitutions via Wheland Complexes ("Ar-S[subscript E] Reactions") / 5.1:
Ar-S[subscript E] Reactions via Wheland Complexes: Individual Reactions / 5.2:
Electrophilic Substitution Reactions on Metallated Aromatic Compounds / 5.3:
Nucleophilic Substitution Reactions in Aryldiazonium Salts / 5.4:
Nucleophilic Substitution Reactions via Meisenheimer Complexes / 5.5:
Nucleophilic Aromatic Substitution via Arynes, cine Substitution / 5.6:
Nucleophilic Substitution Reactions on the Carboxyl Carbon (Except through Enolates) / 6:
C=O-Containing Substrates and Their Reactions with Nucleophiles / 6.1:
Mechanisms, Rate Laws, and Rate of Nucleophilic Substitution Reactions at the Carboxyl Carbon / 6.2:
Activation of Carboxylic Acids and of Carboxylic Acid Derivatives / 6.3:
Selected S[subscript N] Reactions of Heteroatom Nucleophiles on the Carboxyl Carbon / 6.4:
S[subscript N] Reactions of Hydride Donors, Organometallics, and Heteroatom-Stabilized "Carbanions" on the Carboxyl Carbon / 6.5:
Additions of Heteroatom Nucleophiles to Heterocumulenes. Additions of Heteroatom Nucleophiles to Carbonyl Compounds and Follow-up Reactions / 7:
Additions of Heteroatom Nucleophiles to Heterocumulenes / 7.1:
Additions of Heteroatom Nucleophiles to Carbonyl Compounds / 7.2:
Addition of Heteroatom Nucleophiles to Carbonyl Compounds in Combination with Subsequent S[subscript N]1 Reactions: Acetalizations / 7.3:
Addition of Nitrogen Nucleophiles to Carbonyl Compounds in Combination with Subsequent E1 Eliminations: Condensation Reactions of Nitrogen Nucleophiles with Carbonyl Compounds / 7.4:
Addition of Hydride Donors and Organometallic Compounds to Carbonyl Compounds / 8:
Suitable Hydride Donors and Organometallic Compounds and a Survey of the Structure of Organometallic Compounds / 8.1:
Chemoselectivity of the Addition of Hydride Donors to Carbonyl Compounds / 8.2:
Diastereoselectivity of the Addition of Hydride Donors to Carbonyl Compounds / 8.3:
Enantioselective Addition of Hydride Donors to Carbonyl Compounds / 8.4:
Addition of Organometallic Compounds to Carbonyl Compounds / 8.5:
1,4-Additions of Organometallic Compounds to [alpha],[beta]-Unsaturated Ketones / 8.6:
Reaction of Ylides with Saturated or [alpha],[beta]-Unsaturated Carbonyl Compounds / 9:
Ylides/Ylenes / 9.1:
Reactions of S Ylides with Saturated Carbonyl Compounds or with Michael Acceptors: Three-Membered Ring Formation / 9.2:
Condensation of P Ylides with Carbonyl Compounds: Wittig Reaction / 9.3:
Horner-Wadsworth-Emmons Reaction / 9.4:
Chemistry of the Alkaline Earth Metal Enolates / 10:
Basic Considerations / 10.1:
Alkylation of Quantitatively Prepared Enolates and Aza-Enolates; Chain-Elongating Syntheses of Carbonyl Compounds and Carboxylic Acid Derivatives / 10.2:
Hydroxyalkylation of Enolates with Carbonyl Compounds ("Aldol Addition"): Synthesis of [beta]-Hydroxyketones and [beta]-Hydroxyesters / 10.3:
Condensation of Enolates with Carbonyl Compounds: Synthesis of Michael Acceptors / 10.4:
Acylation of Enolates / 10.5:
Michael Additions of Enolates / 10.6:
Rearrangements / 11:
Nomenclature of Sigmatropic Shifts / 11.1:
Molecular Origins for the Occurrence of [1,2]-Rearrangements / 11.2:
[1,2]-Rearrangements in Species with a Valence Electron Sextet / 11.3:
[1,2]-Rearrangements without the Occurrence of a Sextet Intermediate / 11.4:
Claisen Rearrangement / 11.5:
Thermal Cycloadditions / 12:
Driving Force and Feasibility of One-Step [2 + 4]- and [2 + 2]-Cycloadditions / 12.1:
Transition State Structures of Selected One-Step [2 + 4]- and [2 + 2]-Cycloadditions / 12.2:
Diels-Alder Reactions / 12.3:
[2 + 2]-Cycloadditions with Dichloroketene / 12.4:
1,3-Dipolar Cycloadditions / 12.5:
Transition Metal-Mediated Alkenylations, Arylations, and Alkynylations / 13:
Alkenylation and Arylation of Copper-Bound Organyl Groups / 13.1:
Alkenylation and Arylation of Grignard Compounds / 13.2:
Palladium-Catalyzed Alkenylation and Arylation of Organometallic Compounds / 13.3:
Alkynylation of Copper Acetylides / 13.4:
Heck Reactions / 13.5:
Oxidations and Reductions / 14:
Oxidation States of Organic Chemical Compounds, Oxidation Numbers in Organic Chemical Compounds, and Organic Chemical Redox Reactions / 14.1:
Cross-References to Redox Reactions Already Discussed in Chapters 1-13 / 14.2:
Oxidations / 14.3:
Reductions / 14.4:
Index
Foreword
Preface to the English Edition
Preface to the German Edition
6.

図書

図書
editor, Robert W. Taft
出版情報: New York : J. Wiley, c19-  v. ; 24 cm
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Hammett Memorial Lecture / J. Shorter
Thermodynamics of Molecular Species / E. Grunwald
Reaction Coordinates and Structure-Energy Relationships
Theoretical Studies of the Effects of Hydration on Organic Equilibria / R. Topsom
Y x Scales of Solvent Ionizing Power / T. Bentley ; G. Llewellyn
Correlation Analysis of Acidity and Basicity: From the Solution to the Gas Phase / J-F Gal ; P-C Maria
Correlation Analysis in Organic Crystal Chemistry / T. Krygowski
Author Index
Subject Index
Cumulative Index, Volumes 1 to 17
Hammett Memorial Lecture / J. Shorter
Thermodynamics of Molecular Species / E. Grunwald
Reaction Coordinates and Structure-Energy Relationships
7.

図書

図書
Ray Q. Brewster, William McEwen
出版情報: Englewood Cliffs, N.J. : Prentice-Hall, c1961  x, 854 p. ; 24 cm
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8.

図書

図書
ed. by Saul G. Cohen, Andrew Streitwieser, Robert W. Taft
出版情報: New York : Interscience, 1963-  v. ; 24 cm
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9.

図書

図書
O'Donnell, Martin J. ; Scriven, Eric F. V. ; Turnbull, Kenneth ; Ketcha, Daniel M. ; Weintraub, Philip M. ; Wade, L. G., 1947- ; Gross, Raymond S. ; Morrow, Gary W. ; Pinhas, Allan R. ; McMurry, John ; Miller, R. Bryan ; Hegedus, Louis S. ; Wilson, Stephen R. (Stephen Ross), 1946-
出版情報: Orlando ; Tokyo : Academic Press, 1970-  v. ; 23 cm
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Carbon-Carbon Bond Forming Reactions
Oxidations
Reductions
Synthesis of Heterocycles
Protecting Groups
Useful Synthetic Preparations
Reviews
Author Index
Useful Synthesis Preparations
Selected Topical Areas
Preface
List of Journals Abstracted
Glossary of Abbreviations
Carbon-Carbon Single Bonds (see also: I.E., I.F., I.G., I.H.) / I.:
Alkylations of Aldehydes, Ketones, and their Derivatives / 1.:
Alkylations of Nitriles, Acids and Acid Derivatives / 2.:
Alkylations of [beta]-Dicarbonyl, [beta]-Cyanocarbonyl Systems, and Other Active Methylene Compounds / 3.:
Alkylations of N-, P-, S-, Se & Similar Stabilized Carbanions / 4.:
Alkylations of Organometallic Reagents (see also: I.B.3., I.B.4., I.F., I.G.) / 5.:
Other Alkylation Procedures / 6.:
Nucleophilic Addition to Electrophilic Carbon / 7.:
1,2-Additions / a.:
Aldol-Type 1,2 Additions / (1):
Addition of N, P, S, Se & Similar Stabilized Carbanions / (2):
Addition of Organometallic and Related Species / (3):
Other 1,2-Additions / (4):
Conjugate Additions / b.:
Enolate-Type Carbanions
Organometallic and Related Reagents
Other Conjugate Additions
Other Carbon-Carbon Single Bond Forming Reactions / 8.:
Carbon-Carbon Double Bonds (See also: I.E.1) / B.:
Wittig-Type Olefination Reactions
Eliminations
Alcohols and Derivatives
Halides
Other Eliminations / c.:
Olefin Metatheses
Other Carbon-Carbon Double Bond Forming Reactions
Vinylations
Allene Forming Reactions
Carbon-Carbon Triple Bonds / C.:
Cyclopropanations / D.:
Carbene or Carbenoid Additions to a Multiple Bond
Other Cyclopropanations
Thermal and Photochemical Reactions / E.:
Cycloadditions
Other Thermal Reactions
Photochemical Reactions
Aromatic Substitutions Forming a New Carbon-Carbon Bond / F.:
Friedel-Crafts Type Aromatic Substitution Reactions
Coupling Reactions to Form an Aromatic Carbon-Aromatic Carbon Bond
Other Aromatic Substitutions and Preparations
Synthesis via Organometallics / G.:
Synthesis via Organoboranes
Carbonylation Reactions
Other Syntheses via Organometallics
Rearrangements / H.:
Claisen, Cope and Similar Processes
Other Rearrangements
C-O Oxidations / II.:
Alcohol to Ketones, Aldehydes
Alcohols, Aldehydes to Acids, Esters
C-H Oxidations
C-H to C-O
C-H to C-Hal
C-N Oxidations
Amine Oxidations
Sulfur Oxidations
Oxidative Additions to C-C Multiple Bonds
Epoxidations
Hydroxylations
Other Oxidative Additions to C-C Multiple Bonds
Phenol-Quinone Oxidation
Dehydrogenations
Other Oxidations
C=O Reductions (see also III.F.1) / III.:
Aldehydes, Ketones to Alcohols
Acids, Esters, Amides to Aldehydes
Acids, Esters, Amides to Alcohols
Acids, Esters, Anhydrides to Other
C-N Multiple Bond Reductions
Imine Reductions
Reduction of Heterocycles
Reduction of Sulfur Compounds
N-O Reductions
C-C Multiple Bond Reductions
C=C Reductions
C[identical with]C Reductions
Hetero Bond Reductions
C-O to C-H
C-Hal to C-H
C-S to C-H
Reductive Cleavages
Oxiranes
N-O Cleavages
Other Reductive Cleavages
Reduction of Azides
Other Reductions
Oxiranes, Aziridines, and Thiiranes / IV.:
Oxetanes, Azetidines, and Thietanes
Lactams
Lactones
Furans and Thiophenes
Pyrroles, Indoles, etc
Pyridines, Quinolines, etc
Pyrans, Pyrones, and Sulfur Analogues
Other Heterocycles with One Heteroatom
Heterocycles with a Bridgehead Heteroatom / J.:
Heterocycles with Two or More Heteroatoms / K.:
Heterocycles with 2 N's
5-Membered
6-Membered
7-Membered
Heterocycles with 2 O's or 2 S's
Heterocycles with 1 N and 1 O
Heterocycles with 1 N and 1 S
Heterocycles with 1 O and 1 S
Heterocycles with 3 or more N's
Heterocycles with 2 N's and 1 O
Heterocycles with 2 N's and 1 S
Other Heterocycles / L.:
Aldehyde and Ketone Protecting Groups / M.:
Amino Acid Protecting Groups
Amine Protecting Groups
Carboxyl Protecting Groups
Hydroxyl Protecting Groups
Other Protecting Groups
Functional Group Preparations / VI.:
Acetals and Ketals
Acids and Anhydrides
Alcohols and Related Species (see also: II.B.1, III.A., V.E., VI.A.9)
Aldehydes and Ketones (see also: I.A.1., I.G.2., II.A.1)
Amides and Related Species
Amines
Amino Acid Derivatives
Azides
Carbohydrates / 9.:
Esters (see also: I.G.2., IV.D., V.D., VI.A.3) / 10.:
Ethers / 11.:
Halides (see also: II.B.2.) / 12.:
Nitriles and Imines / 13.:
Other N-Containing Functional Groups / 14.:
Additions to Alkenes and Alkynes
Boron Compounds
Nucleosides, Nucleotides, etc
Phosphorus, Selenium and Tellurium Compounds
Silicon Compounds
Sulfur Compounds
Tin Compounds
Techniques / VII.:
Asymmetric Synthesis and Molecular Recognition
Reactions
Reactive Intermediates
Organometallics and Metalloids
Halogen Compounds and Halogenation (see also: VI.A.11.)
Natural Products
Others (see also: IV.M, VIII.A.5, VIII.C.6, VIII.F.7)
Fullerene Chemistry / VIII.:
Diels-Alder Type Cycloadditions
Other Cycloadditions
Other Fullerene Chemistry
Taxol and Related Taxane Chemistry
Dendrimers, Calixarenes and Other Unnatural Products
Dendrimers
Dendrimer Synthesis
Dendrimer Catalysts
Hetero-Containing & Miscellaneous Dendrimers
Calixeranes
Calixarene Receptors
Synthesis of Calixirane
Synthesis on Calixiranes
Calixirane Isolation, Conformation, etc / d.:
Rotaxanes
Supramolecules
Cyclophanes
Other
Total Syntheses of Selected Natural Products (see also: VIII.B and VIII.C)
Reactions in Polar Media
Reactions in Aqueous Media
Reactions in Ionic Media
Combinatorial Chemistry
Supports, Linkers and Protecting Groups
Supported Reagents, Catalysts, Ligands and Scavengers
Solid-Phase Heterocyclic Synthesis
Solid-Supported Organic Reaction Processes
Targeted Library Synthesis
Novel Techniques in Combinatorial Chemistry
Journals Abstracted
Synthesis Of Heterocycles
Selected TopicalAreas
(Chapter Titles) Carbon-Carbon Bond Forming Reactions
AuthorIndex
Carbon-Carbon Bond Forming Reactions
Oxidations
Reductions
10.

図書

図書
American Chemical Society ; Mayo, Frank R.
出版情報: Washington : American Chemical Society, 1968  xv, 364 p. ; 24 cm
シリーズ名: Advances in chemistry series ; 75 . Oxidation of organic compounds ; v. 1
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