close
1.

図書
図書
1. Organic chemistry
Jonathan Clayden ... [et al.]
出版情報: New York : Oxford University Press, 2001  1512 p. ; 28 cm
所蔵情報: loading…
目次情報: 続きを見る
List
What is Organic Chemistry? / 1：
Organic Structures / 2：
Determining Organic Structures / 3：
Structure of Molecules / 4：
Organic Reactions / 5：
Nucleophilic Addition to the C=O Group / 6：
Conjugation/Delocalisation and UV spectra / 7：
Acidity and Basicity of Organic Molecules / 8：
Formation of C-C fromC=O Bonds by Organo-Metallic reagents / 9：
Conjugate Addition and Substitution / 10：
Proton NMR Spectroscopy / 11：
Nucleophilic Substitution at the C=O Group / 12：
Review Chapter: Summary of Mechanistic Principles / 13：
Addition to C=O with Loss of Carbonyl Oxygen / 14：
Review Chapter on SpectroscopicMethods / 15：
Stereochemistry / 16：
Nucleophilic Substitution at Saturated Carbon / 17：
Conformational Analysis / 18：
Elimination Reactions / 19：
Electrophilic Addition to Alkenes / 20：
Formation and Reactions of Enolates / 21：
Electrophilic Aromatic Substitution / 22：
Electrophilic Alkenes: ConjugateAddition, Allylic Systems and Nucleophilic Aromatic Substitution / 23：
Chemoselectivity, Protection, Oxidation and Reductio / 24：
List
What is Organic Chemistry? / 1：
Organic Structures / 2：
2.

図書
図書
2. Advanced organic chemistry : reaction mechanisms
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
所蔵情報: loading…
目次情報: 続きを見る
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
3.

図書
図書
3. Study guide/solutions manual for Jones's Organic Chemistry. 2nd ed
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
所蔵情報: loading…
4.

図書
図書
4. Study guide and solutions manual for fundamentals of organic chemistry. 4th ed
Susan McMurry
出版情報: 東京 : 東京化学同人 (発売), 2000.4  361p ; 24cm
所蔵情報: loading…
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：
文献の複写および貸借の依頼を行う
 文献複写・貸借依頼