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
Stereochemical and synthetic studies of the intramolecular diels-alder reaction / W.R. Roush
Thermal reaction of cyclpropenone ketals, key mechanistic features, scope and application of the cycloaddition reactions of cyclopropene ketals and p - delocalized singlet vinyl carbenes; three crabon 1,1-/ 1,3-dipoles / D.L. Boger ; C.E. Brotherton-Pleiss
Index
Introduction to the series: an editor's foreword / A. Padwa
The Ramberg-Blacklund Rearrangement / Nicolas Agenet ; Leo A. Paquette ; H. Gschwend ; G. A. Boswell, Jr. ; D. Caine ; A. J. Birch ; B. Castro ; S. Areniyadis et al. ; Sara Jane Rhoads ; Olivier BuisineChapter 1：
Reduction and Related Reactions of gamma,B-Unsaturated Compounds with Metals in Liquid Ammonia / R. Rodriguez ; W. C. Ripka
Replacement of Alcoholic Hydroxyl Groups by Halogens and Other Nucleophiles Via Oxyphosphonium Intermediates / D. H. Williamson
Addition and Substitution Reactions of Nitrile-Stabilized Carbanions
Author Index, Volumes 1-31 / William S. Wadsworth Jr. ; N. Rebecca Raulins ; J. J. Bloomfield ; R. Nayori
Homogeneous Hydrogenation Catalysts in Organic Synthesis / R. M. Scribner
Chapter and Topic Index, Volumes 1-31
Synthetic Application of Phosphoryl-Stabilized Anons
The Claisen and Cope Rearrangements / S. Burke
Subject Index, Volume 31 / D. C. Owsley ; J. E. McMurry ; Y. Hayakawa
Ester Cleavages via SN 2-Type Dealkylation / Vincent Gandon ; Wataru Nagata ; C. W. Tullock ; P. Grieco ; Gary H. Posner ; J. M. Nelke2：
Reductive Dehalogenation of Polyhalo Ketones with Low-Valent Metals and Related Reducing Agents
Fluorination by Sulfur Tetrafluorid / Corinne Aubert ; Mitsuru Yoshioka
Intramolecular Reactions of Diazocarbonyl Compounds / C. S. Rondestvedt, Jr. ; J. Crandall
Substitution Reactions Using Organocopper Reagents / Clay M. Sharts
The Acyloin Condensation
Hydrocyanation of Conjugated Carbonyl Compounds / Max Malacria
Author Index, Volumes 1-26
Arylation of Unsaturated Compounds by Diazonium Salts (The Meerwein Arylation Reaction / R. H. Shapiro3：
Author Index, Volumes 1-25 / M. Apparu
Chapter and Topic Index, Volumes 1-26
Chapter and Topic Index, Volumes 1-25 / William A. Sheppard ; E. Vedejs ; N. Rabjohn
Subject Index, Volume 26
Alkenes from Tosylhydrazones
Base Isomerizations of Epoxides
Cotrimerizations of Acetylenic Compounds
Subject Index? Volume 25
Modern Methods to Prepare Monofluoroaliphatic Compounds
Clemmensen Reduction of Ketones in Anhydrous Organic Solvents
Selenium Dioxide Oxidation
Author Index, Volumes 1-29
Author Index, Volumes 1-21 / Chapter 2：
Chapter and Topic Index, Volumes 1-29 / 4：
Chapter Index, Volumes 1-21 / Simone Bufali
Subject Index, Volume 29 / Michael W. Rathke?
Subject Index, Volume 21
The Reformatsky Reaction / Peter H. Seeberger
Author Index, Volumes 1-22?
Chapter and Topic Index, Volumes 1-22?
Glycosylation on Polymer Supports
Subject Index, Volume 22
Cumulative Chapter Titles by Volume
Author Index, Volumes 1-68
Chapter and Topic Index, Volumes 1-68
Chiral Synthons by Ester Hydrolysis Calalyzed by Pig Liver Esterase / M. Ohno ; M. Otsuka
The Electrophilic Substitution of Allylsilanes and Vinylsilanes / I. Fleming et al.
Author Index, Volumes 1-37
Chapter and Topic Index, Volumes 1-37
The Ramberg-Blacklund Rearrangement / Nicolas Agenet ; Leo A. Paquette ; H. Gschwend ; G. A. Boswell, Jr. ; D. Caine ; A. J. Birch ; B. Castro ; S. Areniyadis et al. ; Sara Jane Rhoads ; Olivier BuisineChapter 1：
Reduction and Related Reactions of gamma,B-Unsaturated Compounds with Metals in Liquid Ammonia / R. Rodriguez ; W. C. Ripka
Replacement of Alcoholic Hydroxyl Groups by Halogens and Other Nucleophiles Via Oxyphosphonium Intermediates / D. H. Williamson
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：
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：
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：
Carbon-Bridged Ferrocenophanes / J. Park ; T. Lee5：
Endohedral Metal Complexes of Cyclophanes / R. Gleiter, et al.6：
Intramolecular Reactions in Cyclophanes / H. Hopf7：
Reactive Intermediates from Cyclophanes / W. Sander8：
X-Ray Crystal Structures of Porphyrinophanes as Model Compounds for Photoinduced Electron Transfer / H. Irngartinger ; T. Oeser9：
Ultraviolet Photoelectron Spectra of Cyclophanes / H. Muchall10：
UV/Vis Spectra of Cyclophanes / P. Rademacher11：
Electronic Circular Dichroism of Cyclophanes / S. Grimme ; A. Bahlmann12：
Fully Conjugated Beltenes (Belt-Like and Tubular Aromatics / R. Herges13：
Molecular Electrochemistry of Cyclophanes / B. Speiser14：
NMR Spectra of Cyclophanesn / L. Ernst and K.Ibrom15：
Strained Heteroatom-Bridged Metallocenophanes / I. Manners ; U. Vogel16：
Cyclophanes as Templates in Stereoselective Synthesis / V. Rozenberg, et al.17：
Vapor-Based Polymerization of Functionalized [2.2] Paracyclophanes: A Unique Approach towards Surface-Engineered Microenvironments / D. Kell, et al.18：
From Cyclophanes to Molecular Machines / A. Flood, et al.19：
Molecular Recognition Studies with Cyclophane Receptors in Aqueous Solutions / F. Diederich20：
Hetera / Cyclo-)phanes ; F. Vgtle ; et alSubject Index：
Asymmetric Synthesis Of Epoxides And Aziridines From Aldehydes And Imines
Asymmetric Epoxidation of Carbonyl Compounds Asymmetric Aziridination of Imines Vinylaziridines In Organic Synthesis
Direct Synthesis of Vinylaziridines Ring-opening Reactions with Nucleophiles Isomerization Including Rearrangement Cycloaddition Electron Transfer to Vinylaziridines
Asymmetric Syntheses With Aziridinecarboxylate And Aziridinephosphonate Building Blocks
Preparation of Aziridine-2-carboxylates and Aziridine-2-phosphonates Reactions of Aziridine-2-carboxylates and Aziridine-2-phosphonates Applications in Natural Product Syntheses
Synthesis Of Aziridines
Overview and General Features
Metalated Epoxides And Aziridines In Synthesis
Metalated Epoxides Metalated Aziridines
Metal-Catalyzed Synthesis Of Epoxides
Oxidants Available for Selective Transition Metal-catalyzed Epoxidation
Epoxidations of Olefins Catalyzed by Early Transition Metals Chromium
Enantioselective Nucleophilic Addition to Meso-Epoxides
Kinetic Resolution of Racemic Epoxides Enantioselective Rearrangements of Epoxides
Epoxides In Complex Molecule Synthesis
Synthesis of Complex Molecules by Intramolecular Ring-opening of Epoxides with Heteronucleophiles
Synthesis of Complex Molecules by Ring-opening of Epoxides with C-Nucleophiles Epoxy Glycals Synthesis of Complex Molecules by Rearrangement Reactions of Epoxides
Vinylepoxides In Organic Synthesis
Synthesis of Vinylepoxides Transformations of Vinylepoxides
The Biosynthesis Of Epoxides
Cytochrome P450 Monooxygenases Flavin-dependent Epoxidases Dioxygenases Epoxidation through Dehydrogenation Dehalogenases
Aziridine Natural Products
Discovery, Biological Activity And Biosynthesis
Mitomycins and Related Natural Products
The Azinomycins Other Aziridine Natural Products
Epoxides And Aziridines In Click Chemistry
Epoxides in Click Chemistry Aziridines in Click Chemistry
Aziridinium Ions in Click Chemistry
Asymmetric Synthesis Of Epoxides And Aziridines From Aldehydes And Imines
Asymmetric Epoxidation of Carbonyl Compounds Asymmetric Aziridination of Imines Vinylaziridines In Organic Synthesis
Direct Synthesis of Vinylaziridines Ring-opening Reactions with Nucleophiles Isomerization Including Rearrangement Cycloaddition Electron Transfer to Vinylaziridines
図書
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