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1.

図書
図書
1. Seminars in organic synthesis : XXVI Summer School "A. Corbella" : June 18-22, 2001 Palazzo Feltrinelli Università degi Studi di Milano Gargnano(BS)
Società Chimica Italiana Divisione di Chimica Organica
出版情報: [Milano] : Società Chimica Italiana, 2001  695 p. ; 24 cm
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Giancarlo Jommi Memorial Lectures
Dipole-stabilized Carbanions. The Complex Induced Proximity Effect. The Endocyclic Restriction Test. Dynamic Thermodynamic Resolution / P. Beak
Carbohydrates for the Life Science
Glycal of Common Monosaccharides: Useful Intermediates for the Synthesis of Rare Bioactive Carbohydrates / G. Catelani ; F. D'andrea
Glycidic Scaffolds in Peptidomimetics Synthesis / F. Nicotra ; F. Peri ; L. Cipolla ; E. Forni ; B. La Ferla ; E. Caneva
Methods for Carbon-Linked Glycosyl Amino Acid Synthesis. The Gateway to Artificial Glycopeptides / A. Dondoni
NMR Spectroscopic Methods for the Determination of Stereogenic Elements
Selected NMR Techniques for the Determination of Absolute Configuration / Donatella Potenza
Relative Configuration Analysis of Flexible Systems by NMR Spectroscopy / L. Gomez-Paloma ; G. Bifulco ; C. Bassanello ; P. Cimino
Special Organometallic Bases in Organic Synthesis
Organometallic Bases Induced Rearrangements / A. Mordini ; M. Valacchi
Oxiranyl and Aziridinyl Anions: Applications in Synthesis / S. Florio
Low Environmental Impact Processes
Low Environmental Impact Processes in the Pharmaceutical Industry / T. Rossi
Recent Advances in Polymer Assisted Solution Phase Synthesis / L. Raveglia
Ethics of Research
Critical Surveys Covering the Year 2000 / G. Marino
Introduction and Transformation of Functional Groups / A. Marra
Solid Supported Synthesis / E. Perrotta
Total Synthesis of Natural Products / L. Lay ; F. Compostella
Compounds in Organic Synthesis / M. Comes-Franchini
Giancarlo Jommi Memorial Lectures
Dipole-stabilized Carbanions. The Complex Induced Proximity Effect. The Endocyclic Restriction Test. Dynamic Thermodynamic Resolution / P. Beak
Carbohydrates for the Life Science
2.

図書
図書
2. Organic chemistry
Jonathan Clayden ... [et al.]
出版情報: New York : Oxford University Press, 2001  1512 p. ; 28 cm
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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：
3.

図書
図書
3. Photoinduced charge transfer : proceedings of the 10th annual symposium of the NSF center, University of Rochester, Rochester, New York, 26-29 July 1999
editor, Lewis Rothberg ; [sponsored by the National Science Foundation Center]
出版情報: Singapore : World Scientific, c2000  ix, 232 p. ; 23 cm
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4.

図書
図書
4. 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
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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
5.

図書
図書
5. Seminars in organic synthesis : XXV Summer School "A. Corbella" : June 12-16, 2000 Palazzo Feltrinelli Università degi Studi di Milano Gargnano(BS)
Società chimica italiana Divisione di chimica organica
出版情報: [Milano] : Società chimica italiana, 2001  1 v. (various pagings) ; 24 cm
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6.

図書
図書
6. Systematic nomenclature of organic, organometallic and coordination chemistry : chemical-abstracts guidelines with IUPAC recommendations and many trivial names ([EPFL Press] ; [CRC Press])
Ursula Bünzli-Trepp
出版情報: Lausanne : EPFL Press, c2007  ix, 636 p. ; 30 cm.
シリーズ名: Fundamental sciences ; Chemistry
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Directions for Use of the Book / 1：
Fundamentals / 2：
Nomenclature terms and definitions used in the Book / 2.1：
Conventions for enclosing marks and vowels in names / 2.2：
Enclosing marks / 2.2.1：
Vowels / 2.2.2：
Guide to Name Construction and Name Interpretation / 3：
General procedure and choice of the senior compound class (choice of the principal group) / 3.1：
Nomenclature types / 3.2：
Substitutive nomenclature / 3.2.1：
Conjunctive nomenclature / 3.2.2：
Multiplicative nomenclature: compounds with identical structural units / 3.2.3：
Additive nomenclature / 3.2.4：
Subtractive nomenclature / 3.2.5：
Functional-class nomenclature / 3.2.6：
Determination of the molecular-skeleton parent / 3.3：
Numbering of the molecular-skeleton parent and of other structure components / 3.4：
Alphabetical order of prefixes or parent-substituent names / 3.5：
Molecular-Skeleton Parents / 4：
Preliminary notes / 4.1：
Hydrocarbon chains / 4.2：
Heterochains / 4.3：
Heterochains with irregularly placed heteroatoms: replacement nomenclature ('a' nomenclature) / 4.3.1：
Heterochains with regularly placed heteroatoms: homogeneous and heterogeneous heterochains / 4.3.3：
Carbomonocycles / 4.4：
Heteromonocycles / 4.5：
Heteromonocycles with compulsory trivial names / 4.5.1：
Heteromonocycles with ten or fewer ring members: extended Hantzsch-Widman nomenclature / 4.5.3：
Heteromonocycles with more than ten ring members: replacement nomenclature ('a' nomenclature) / 4.5.4：
Silicon-containing heteromonocycles / 4.5.5：
Fused polycycles (carbo- and heterocycles) / 4.6：
Fused polycycles with compulsory semitrivial or trivial names / 4.6.1：
Fused polycycles consisting of a parent component and attached components: fusion names / 4.6.3：
Fused polycycles with replacement names ('a' names) / 4.6.4：
Von Baeyer bridged polycycles (carbo- and heterocycles) / 4.7：
Bridged fused polycycles (carbo- and heterocycles) / 4.8：
Spiropolycycles (carbo- and heterocycles) / 4.9：
Spiropolycycles with carbomonocycle or heteromonocycle components / 4.9.1：
Spiropolycycles with at least one fused-polycycle component or one von Baeyer bridged-polycycle component / 4.9.3：
Ring assemblies of identical ring components (carbo- and heterocycles) / 4.10：
Substituent Prefixes / 5：
Prefixes of mononuclear substituents / 5.1：
Prefixes of hydrocarbon-chain substituents / 5.3：
Prefixes of heterochain substituents / 5.4：
Prefixes of carbocycle substituents / 5.5：
Prefixes of heterocycle substituents / 5.6：
Prefixes of ring-assembly substituents / 5.7：
Prefixes of composite substituents: choice of the parent substituent / 5.8：
Prefixes of carbonyl-containing substituents and analogs / 5.9：
Compound Classes / 6：
Radicals / 6.1：
Radical center at a molecular-skeletal parent / 6.2.1：
Radical center at a characteristic group / 6.2.3：
Polyradicals / 6.2.4：
Cations / 6.3：
Cation center by the formal addition of electrophiles E[superscript +] / 6.3.1：
Cation center by the formal removal of hydride ions H[superscript -] / 6.3.3：
Cation center resulting from skeletal bonding of a heteroatom / 6.3.4：
Cation center in spiropolycycles / 6.3.5：
Cation substituents (prefixes) / 6.3.6：
Polycations / 6.3.7：
Anions / 6.4：
Anion center by the formal removal of protons H[superscript +] / 6.4.1：
Anion center by the formal addition of hydride ions H[superscript -] / 6.4.3：
Anion substituents (prefixes) / 6.4.4：
Polyanions / 6.4.5：
Zwitterions / 6.5：
Radical ions / 6.6：
Carboxylic, carbothioic, carboselenoic, carbotelluroic, carbohydrazonic, carboximidic, and corresponding carboperoxoic acids and salts / 6.7：
Carboxylic acids / 6.7.1：
Carbothioic, carboselenoic, carbotelluroic, carbohydrazonic, and carboximidic acids / 6.7.3：
Carboperoxoic acids (peroxy acids) and their chalcogeno, hydrazono, and imido replacement analogs / 6.7.4：
Salts of carboxylic acids and of their chalcogeno, hydrazono, imido, and peroxy replacement analogs / 6.7.5：
Sulfonic, sulfinic, and sulfenic acids, selenonic, seleninic, and selenenic acids, telluronic, tellurinic, and tellurenic acids, their chalcogeno, hydrazono, imido, and peroxy replacement analogs, and corresponding salts / 6.8：
C-Oxoacids: carbonic and formic acid and their replacement analogs and corresponding salts / 6.9：
S-, Se-, Te-, and N-Oxoacids / 6.10：
P- and As-Oxoacids / 6.11：
Sb-, Bi-, Si-, and B-Oxoacids / 6.12：
Anhydrides / 6.13：
Esters and lactones / 6.14：
Acid halides / 6.15：
Amides, lactams, cyclic imides, and amidines / 6.16：
Hydrazides / 6.17：
Nitriles / 6.18：
Aldehydes and their oxime and hydrazone derivatives / 6.19：
Ketones and their oxime and hydrazone derivatives / 6.20：
Alcohols and phenols / 6.21：
Hydroperoxides / 6.22：
Amines / 6.23：
Imines / 6.24：
Nitrogen compounds / 6.25：
Phosphorus and arsenic compounds / 6.26：
Antimony and bismuth compounds / 6.27：
Boron compounds / 6.28：
Silicon, germanium, tin, and lead compounds / 6.29：
Oxygen compounds / 6.30：
Sulfur, selenium, and tellurium compounds / 6.31：
Carbon compounds / 6.32：
Halogen compounds / 6.33：
Organometallic and coordination compounds / 6.34：
Appendixes
Specialist nomenclatures / A.1：
Alkaloids / A.1.1：
Amino acids and peptides / A.1.3：
Carbohydrates / A.1.4：
Cyclitols / A.1.5：
Nucleosides, nucleotides, and nucleic acids / A.1.6：
Steroids / A.1.7：
Terpenes, carotenoids, and retinoids / A.1.8：
Vitamins / A.1.9：
Porphyrins and bile pigments / A.1.10：
Polymers / A.1.11：
References for specific compound classes, Internet addresses, and nomenclature software / A.1.12：
Multiplying affixes / A.2：
Modifying syllables / A.3：
Heteroatom syllables and element names / A.4：
Indicated H atom 'H' (indicated hydrogen) / A.5：
Configuration descriptors in names / A.6：
Definitions / A.6.1：
The CIP system for the specification of the configuration of a stereogenic center, axis or plane, or double bond / A.6.2：
Stereodescriptors for the denotation of the absolute and relative configuration in names / A.6.3：
Configuration of organometallic and coordination compounds / A.6.4：
Lambda ([lambda]) convention / A.7：
Isotopically modified compounds / A.8：
Isotopically modified compounds: IUPAC Recommendations / A.8.1：
Isotopically modified compounds: CA Guidelines / A.8.3：
Index
Directions for Use of the Book / 1：
Fundamentals / 2：
Nomenclature terms and definitions used in the Book / 2.1：
7.

図書
図書
7. Study guide and student solutions manual for McMurry's Organic chemistry. 第7版
Susan McMurry [著]
出版情報: Belmont, Calif. : Brooks/Cole , 東京 : 東京化学同人 (発売), c2008  900 p ; 28cm
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8.

図書
図書
8. Study guide/solutions manual for Jones's Organic chemistry. 3rd ed (: [ja] ; : [us])
Maitland Jones, Jr. and Henry L. Gingrich
出版情報: New York : Norton , 東京 : 東京化学同人(発売), 2006, c2005  x, 803 p. ; 28 cm
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9.

図書
図書
9. Transition metal carbonyl cluster chemistry
Paul J. Dyson and J. Scott Mclndoe
出版情報: Amsterdam : Gordon and Breach Science, c2000  xi, 166 p. ; 26 cm
シリーズ名: Advanced chemistry texts ; v. 2
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Foreword
Preface
Introduction / Chapter 1：
Definition and Scope / 1.1：
Transition Metal Carbonyl Clusters / 1.2：
When Does a Cluster Become Metal-like? / 1.2.1：
Growth in Transition Metal Carbonyl Cluster Chemistry / 1.2.2：
Electron Counting and Metal-Metal Bonding / Chapter 2：
The Ligands / 2.1：
The Eighteen-Electron Rule / 2.2：
The Effective Atomic Number (EAN) Rule / 2.3：
Wade's Rules / 2.4：
The Isolobal Principle / 2.5：
Polyhedral Skeletal Electron Pair Theory (PSEPT) / 2.6：
The Capping Principle / 2.7：
Condensed Polyhedra / 2.8：
Structure / Chapter 3：
Mononuclear and Dinuclear Complexes / 3.1：
Trinuclear and Tetranuclear Clusters / 3.2：
Pentanuclear and Hexanuclear Clusters / 3.3：
Capped Polyhedra / 3.4：
Coupled and Condensed Polyhedra / 3.5：
Open and Planar Clusters / 3.6：
Larger Clusters / 3.7：
Clusters with Metal-Metal Multiple Bonds / 3.8：
Ligands / Chapter 4：
Carbon Monoxide / 4.1：
Bonding Modes of CO / 4.1.1：
Other Effects / 4.1.2：
Ligands Related to CO / 4.2：
Phosphorus Ligands / 4.3：
Interstitial Main Group Atoms / 4.4：
Hydride Ligands / 4.5：
Unsaturated Organic Ligands / 4.6：
Alkene and Alkyne Ligands / 4.6.1：
Unsaturated Rings / 4.6.2：
Other Ligands / 4.7：
Characterisation Techniques / Chapter 5：
Infrared Spectroscopy / 5.1：
Mass Spectrometry / 5.2：
Nuclear Magnetic Resonance Spectroscopy / 5.3：
[superscript 1]H NMR Spectroscopy / 5.3.1：
Variable-temperature NMR Spectroscopy / 5.3.2：
[superscript 13]C NMR Spectroscopy / 5.3.3：
X-ray Crystallography / 5.4：
Representations of X-ray Structures / 5.4.1：
Disorder / 5.4.2：
Neutron Diffraction / 5.4.3：
Miscellaneous Characterisation Techniques / 5.5：
Electron Paramagnetic Resonance Spectroscopy / 5.5.1：
UV-visible Spectroscopy / 5.5.2：
Mossbauer Spectroscopy / 5.5.3：
Cluster-surface Analogy / 5.6：
Synthesis / Chapter 6：
Simple Homoleptic Carbonyls / 6.1：
High Nuclearity Carbonyl Clusters / 6.2：
Preparation from Salts / 6.2.1：
Thermolysis and Pyrolysis / 6.2.2：
Reduction and Oxidation / 6.2.3：
Redox Condensation Reactions / 6.2.4：
Cluster Build-up Reactions from Preformed High Nuclearity Clusters / 6.2.5：
Reactivity / Chapter 7：
Reduction / 7.1：
Protonation / 7.2：
Substitution / 7.3：
Association and Dissociation / 7.4：
Oxidative Addition and Reductive Elimination / 7.5：
Carbide Formation / 7.6：
Cluster Decomposition Reactions / 7.7：
Reactions with Organic Ligands / Chapter 8：
Alkyl and Alkylidyne Clusters / 8.1：
Alkenes, Alkynes and Allyls / 8.2：
C[subscript 5]-Rings / 8.3：
C[subscript 6]-Rings / 8.4：
C[subscript 7] and C[subscript 8]-Rings / 8.5：
Heterocycles / 8.6：
Heteronuclear Carbonyl Clusters / Chapter 9：
Condensation Reactions / 9.1：
Ligand Displacement / 9.1.2：
Addition Reactions / 9.1.3：
Redox Condensation / 9.1.4：
Bridging Ligands / 9.1.5：
Condensation with Electrophilic Capping Groups / 9.1.6：
Serendipitous Syntheses / 9.1.7：
Heterosite Reactivity / 9.2：
Organic Transformations Using Stoichiometric and Catalytic Quantities of Clusters / Chapter 10：
Establishing Catalysis by Clusters / 10.1：
Hydrogenation Reactions / 10.2：
Hydroformylation / 10.3：
The Water-Gas Shift Reaction / 10.4：
C-H Bond Activation and C-C Bond Formation / 10.5：
Mixed-metal Clusters in Catalysis / 10.6：
Supported Cluster Catalysis and Use of Non-organic Solvents / 10.7：
Solid Supported Clusters / 10.7.1：
Biphasic 'Liquid-liquid' Supports / 10.7.2：
Further Reading
Index
Cluster Formula Index
Foreword
Preface
Introduction / Chapter 1：
10.

図書
図書
10. 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
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