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1.

図書
図書
1. Advanced problems in organic reaction mechanisms. 1st ed (: hardcover ; : flexicover)
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
2.

図書
図書
2. Handbook of palladium catalysed organic reactions : synthetic aspects and catalytic cycles
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)
3.

図書
図書
3. Oxidations in organic chemistry (: pbk)
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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Oxidation Agents
Dehydrogenations
Oxidations
Preparative Procedures
Oxidation Agents
Dehydrogenations
Oxidations
4.

図書
図書
4. Organic chemistry
Marye Anne Fox, James K. Whitesell
出版情報: Boston : Jones and Bartlett, c1994  xxvi, 870 p. ; 29 cm
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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：
5.

図書
図書
5. Fundamentals of organic chemistry. 3rd ed
John McMurry
出版情報: Pacific Grove, Calif. : Brooks/Cole Pub. Co., c1994  xx, 536, 16 p. ; 25 cm
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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：
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