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1.

図書
図書
1. Organic chemistry. 5th ed (:[text] ; :CD-ROM)
John McMurry
出版情報: Pacific Grove, CA : Brooks/Cole Pub. Co., c2000  xliii, 1284, 56, 28 p. ; 26 cm.
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2.

図書
図書
2. Study guide and solutions manual for McMurry's organic chemistry. 5th ed (: [us. hbk.] ; : [us. pbk.] ; : [Ja. pbk.])
Susan McMurry
出版情報: Pacific Grove, Calif. : Brooks/Cole, c2000 , Tokyo : 東京化学同人 (発売), 2001.4  845 p. ; 28 cm
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3.

図書
図書
3. Industrial organic chemistry. 4th completely revised ed / translated by Charlet R. Lindley and Stephen Hawkins
Klaus Weissermel, Hans-Jürgen Arpe
出版情報: Weinheim : Wiley-VCH, 2003  xix, 491 p. ; 25 cm
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Various Aspects of Energy and Raw Material Supply / 1：
Basic Products of Industrial Syntheses / 2：
Olefins / 3：
Acetylene / 4：
1,3-Diolefins / 5：
Syntheses Involving Carbon Monoxide / 6：
Oxidation Products of Ethylene / 7：
Alcohols / 8：
Vinyl-Halogen and Vinyl-Oxygen Compounds / 9：
Components for Polyamides / 10：
Propene Conversion Products / 11：
Aromatics - Production and Conversion / 12：
Benzene Derivatives / 13：
Oxidation Products of Xylene and Naphthalene / 14：
Appendix / 15：
Index
Various Aspects of Energy and Raw Material Supply / 1：
Basic Products of Industrial Syntheses / 2：
Olefins / 3：
4.

図書
図書
4. Name reactions : a collection of detailed reaction mechanisms. 2nd ed
Jie Jack Li
出版情報: Berlin ; Tokyo : Springer, c2003  xviii, 465 p. ; 25 cm
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Abbreviations
Abnormal Claisen rearrangement / 1：
Alder ene reaction / 2：
Aldol condensation / 3：
Allan-Robinson reaction / 4：
Alper carbonylation / 5：
Amadori rearrangement / 6：
Angeli-Rimini hydroxamic acid synthesis / 7：
ANRORC mechanism / 8：
Arndt-Eistert homologation / 9：
Auwers reaction / 10：
Baeyer-Drewson indigo synthesis / 11：
Baeyer-Villiger oxidation / 12：
Baker-Venkataraman rearrangement / 13：
Bamberger rearrangement / 14：
Bamford-Stevens reaction / 15：
Bargellini reaction / 16：
Bartoli indole synthesis / 17：
Barton decarboxylation / 18：
Barton-McCombie deoxygenation / 19：
Barton nitrite photolysis / 20：
Baylis-Hillman reaction / 21：
Beckmann rearrangement / 22：
Beirut reaction / 23：
Benzilic acid rearrangement / 24：
Benzoin condensation / 25：
Bergman cyclization / 26：
Biginelli pyrimidone synthesis / 27：
Birch reduction / 28：
Bischler-Möhlau indole synthesis / 29：
Bischler-Napieralski reaction / 30：
Blaise reaction / 31：
Blanc chloromethylation reaction / 32：
Boekelheide reaction / 33：
Boger pyridine synthesis / 34：
Boord reaction / 35：
Borsche-Drechsel cyclization / 36：
Boulton-Katritzky rearrangement / 37：
Bouveault aldehyde synthesis / 38：
Bouveault-Blanc reduction / 39：
Boyland-Sims oxidation / 40：
Bradsher reaction / 41：
Brook rearrangement / 42：
Brown hydroboration reaction / 43：
Bucherer carbazole synthesis / 44：
Bucherer reaction / 45：
Bucherer-Bergs reaction / 46：
Buchner-Curtius-Schlotterbeck reaction / 47：
Buchner method of ring expansion / 48：
Buchwald-Hartwig C-N bond and C-O bond formation reactions / 49：
Burgess dehydrating reagent / 50：
Cadiot-Chodkiewicz coupling / 51：
Cannizzaro dispropotionation reaction / 52：
Carroll rearrangement / 53：
Castro-Stephens coupling / 54：
Chapman rearrangement / 55：
Chichibabin amination reaction / 56：
Chichibabin pyridine synthesis / 57：
Chugaev reaction / 58：
Ciamician-Dennsted rearrangement / 59：
Claisen condensation / 60：
Claisen rearrangement / 61：
Clarke-Eschweiler reductive alkylation of amines / 62：
Clemmensen reduction / 63：
Combes quinoline synthesis / 64：
Conrad-Limpach reaction / 65：
Cook-Heilbron thiazole synthesis / 66：
Cope elimination reaction / 67：
Cope, oxy-Cope, and anionic oxy-Cope rearrangements / 68：
Corey-Bakshi-Shibata (CBS) reduction / 69：
Corey-Chaykovsky reaction / 70：
Corey-Fuchs reaction / 71：
Corey-Kim oxidation / 72：
Corey-Winter olefin synthesis / 73：
Cornforth rearrangement / 74：
Criegee glycol cleavage / 75：
Criegee mechanism of ozonolysis / 76：
Curtius rearrangement / 77：
Dakin oxidation / 78：
Dakin-West reaction / 79：
Danheiser annulation / 80：
Darzens glycidic ester condensation / 81：
Davis chiral oxaziridine reagent / 82：
de Mayo reaction / 83：
Demjanov rearrangement / 84：
Dess-Martin periodinane oxidation / 85：
Dieckmann condensation / 86：
Diels-Alder reaction / 87：
Dienone-phenol rearrangement / 88：
Di-?-methane rearrangement / 89：
Doebner reaction / 90：
Doebner-von Miller reaction / 91：
Doering-LaFlamme allene synthesis / 92：
Dornow-Wiehler isoxazole synthesis / 93：
Dötz reaction / 94：
Dowd ring expansion / 95：
Dutt-Wormall reaction / 96：
Eglinton reaction / 97：
Eschenmoser coupling reaction / 98：
Eschenmoser-Tanabe fragmentation / 99：
Étard reaction / 100：
Evans aldol reaction / 101：
Favorskii rearrangement and Quasi-Favorskii rearrangement / 102：
Feist-Bénary furan synthesis / 103：
Ferrier rearrangement / 104：
Finkelstein reaction / 105：
Fischer-Hepp rearrangement / 106：
Fischer indole synthesis / 107：
Fischer-Speier esterification / 108：
Fleming oxidation / 109：
Forster reaction / 110：
Frater-Seebach alkylation / 111：
Friedel-Crafts reaction / 112：
Friedländer synthesis / 113：
Fries rearrangement / 114：
Fritsch-Buttenberg-Wiechell rearrangement / 115：
Fujimoto-Belleau reaction / 116：
Fukuyama amine synthesis / 117：
Gabriel synthesis / 118：
Gassman indole synthesis / 119：
Gattermann-Koch reaction / 120：
Gewald aminothiophene synthesis / 121：
Glaser coupling / 122：
Gomberg-Bachmann reaction / 123：
Gribble indole reduction / 124：
Gribble reduction of diaryl ketones / 125：
Grignard reaction / 126：
Grob fragmentation / 127：
Guareschi-Thorpe condensation / 128：
Hajos-Wiechert reaction / 129：
Haller-Bauer reaction / 130：
Hantzsch pyridine synthesis / 131：
Hantzsch pyrrole synthesis / 132：
Haworth reaction / 133：
Hayashi rearrangement / 134：
Heck reaction / 135：
Hegedus indole synthesis / 136：
Hell-Volhardt-Zelinsky reaction / 137：
Henry reaction (nitroaldol reaction) / 138：
Herz reaction / 139：
Heteroaryl Heck reaction / 140：
Hiyama cross-coupling reaction / 141：
Hoch-Campbell aziridine synthesis / 142：
Hodges-Vedejs metallation of oxazoles / 143：
Hofmann rearrangement (Hofmann degradation reaction) / 144：
Hofmann-Löffler-Freytag reaction / 145：
Hofmann-Martius reaction (Reilly-Hickinbottom rearrangement) / 146：
Hooker oxidation / 147：
Horner-Wadsworth-Emmons reaction / 148：
Houben-Hoesch synthesis / 149：
Hunsdiecker reaction / 150：
Ing-Manske procedure / 151：
Jacobsen-Katsuki epoxidation / 152：
Jacobsen rearrangement / 153：
Japp-Klingemann hydrazone synthesis / 154：
Julia-Lythgoe olefination / 155：
Kahne glycosidation / 156：
Keck stereoselective allylation / 157：
Keck macrolactonization / 158：
Kemp elimination / 159：
Kennedy oxidative cyclization / 160：
Kharasch addition reaction / 161：
Knoevenagel condensation / 162：
Knorr pyrrole synthesis / 163：
Koch carbonylation reaction (Koch-Haaf carbonylation reaction) / 164：
Koenig-Knorr glycosidation / 165：
Kolbe electrolytic coupling / 166：
Kolbe-Schmitt reaction / 167：
Kostanecki reaction / 168：
Krapcho decarboxylation / 169：
Kröhnke reaction (pyridine synthesis) / 170：
Kumada cross-coupling reaction / 171：
Larock indole synthesis / 172：
Lawesson's reagent / 173：
Leuckart-Wallach reaction / 174：
Lieben haloform reaction / 175：
Liebeskind-Srogl coupling / 176：
Lossen rearrangement / 177：
Luche reduction / 178：
McFadyen-Stevens reduction / 179：
McLafferty rearrangement / 180：
McMurry coupling / 181：
Madelung indole synthesis / 182：
Mannich reaction / 183：
Marshall boronate fragmentation / 184：
Martin's sulfurane dehydrating reagent / 185：
Masamune-Roush conditions / 186：
Meerwein arylation / 187：
Meerwein-Ponndorf-Verley reduction / 188：
Meinwald rearrangement / 189：
Meisenheimer complex / 190：
Meisenheimer rearrangement / 191：
Meyer-Schuster rearrangement / 192：
Michael addition / 193：
Michaelis-Arbuzov phosphonate synthesis / 194：
Midland reduction / 195：
Miller-Loudon-Snyder nitrile synthesis / 196：
Mislow-Evans rearrangement / 197：
Mitsunobu reaction / 198：
Miyaura boration reaction / 199：
Moffatt oxidation / 200：
Morgan-Walls reaction (Pictet-Hubert reaction) / 201：
Mori-Ban indole synthesis / 202：
Morin rearrangement / 203：
Mukaiyama aldol reaction / 204：
Mukaiyama esterification / 205：
Myers-Saito cyclization / 206：
Nametkin rearrangement (retropinacol rearrangement) / 207：
Nazarov cyclization / 208：
Neber rearrangement / 209：
Nef reaction / 210：
Negishi cross-coupling reaction / 211：
Nenitzescu indole synthesis / 212：
Nicholas reaction / 213：
Noyori asymmetric hydrogenation / 214：
Nozaki-Hiyama-Kishi reaction / 215：
Oppenauer oxidation / 216：
Orton rearrangement / 217：
Overman rearrangement / 218：
Paal-Knorr furan synthesis / 219：
Paal-Knorr pyrrole synthesis / 220：
Parham cyclization / 221：
Passerini reaction / 222：
Paterno-Büchi reaction / 223：
Pauson-Khand cyclopentenone synthesis / 224：
Payne rearrangement / 225：
Pechmann condensation (coumarin synthesis) / 226：
Pechmann pyrazole synthesis / 227：
Perkin reaction (cinnamic acid synthesis) / 228：
Perkow vinyl phosphate synthesis / 229：
Peterson olefination / 230：
Pfau-Plattner azulene synthesis / 231：
Pfitzinger quinoline synthesis / 232：
Pictet-Gams isoquinoline synthesis / 233：
Pictet-Spengler tetrahydroisoquinoline synthesis / 234：
Pinacol rearrangement / 235：
Pinner synthesis / 236：
Polonovski reaction / 237：
Polonovski-Potier rearrangement / 238：
Pomeranz-Fritsch reaction / 239：
Prévost trans-dihydroxylation / 240：
Prilezhaev reaction / 241：
Prins reaction / 242：
Pschorr ring closure / 243：
Pummerer rearrangement / 244：
Ramberg-Bäcklund olefin synthesis / 245：
Reformatsky reaction / 246：
Regitz diazo synthesis / 247：
Reimer-Tiemann reaction / 248：
Reissert reaction (aldehyde synthesis) / 249：
Riley oxidation (selenium dioxide oxidation) / 250：
Ring-closing metathesis (RCM) using Grubbs and Schrock catalysts / 251：
Ritter reaction / 252：
Robinson annulation / 253：
Robinson-Schöpf reaction / 254：
Rosenmund reduction / 255：
Roush allylboronate reagent / 256：
Rubottom oxidation / 257：
Rupe rearrangement / 258：
Rychnovsky polyol synthesis / 259：
Sakurai allylation reaction (Hosomi-Sakurai reaction) / 260：
Sandmeyer reaction / 261：
Sarett oxidation / 262：
Schiemann reaction (Balz-Schiemann reaction) / 263：
Schlosser modification of the Wittig reaction / 264：
Schmidt reaction / 265：
Schmidt's trichloroacetimidate glycosidation reaction / 266：
Scholl reaction / 267：
Schöpf reaction / 268：
Schotten-Baumann reaction / 269：
Shapiro reaction / 270：
Sharpless asymmetric amino hydroxylation / 271：
Sharpless asymmetric epoxidation / 272：
Sharpless dihydroxylation / 273：
Shi asymmetric epoxidation / 274：
Simmons-Smith reaction / 275：
Simonini reaction / 276：
Simonis chromone cyclization / 277：
Skraup quinoline synthesis / 278：
Smiles rearrangement / 279：
Sommelet reaction / 280：
Sommelet-Hauser (ammonium ylide) rearrangement / 281：
Sonogashira reaction / 282：
Staudinger reaction / 283：
Stetter reaction (Michael-Stetter reaction) / 284：
Stevens rearrangement / 285：
Stieglitz rearrangement / 286：
Still-Gennari phosphonate reaction / 287：
Stille coupling / 288：
Stille-Kelly reaction / 289：
Stobbe condensation / 290：
Stollé synthesis / 291：
Stork enamine reaction / 292：
Strecker amino acid synthesis / 293：
Suzuki coupling / 294：
Swern oxidation / 295：
Tamao-Kumada oxidation / 296：
Tebbe olefination (Petasis alkenylation) / 297：
Thorpe-Ziegler reaction / 298：
Tiemann rearrangement / 299：
Tiffeneau-Demjanov rearrangement / 300：
Tishchenko reaction / 301：
Tollens reaction / 302：
Tsuji-Trost allylation / 303：
Ueno-Stork cyclization / 304：
Ugi reaction / 305：
Ullmann reaction / 306：
Vilsmeier-Haack reaction / 307：
von Braun reaction / 308：
von Richter reaction / 309：
Wacker oxidation / 310：
Wagner-Meerwein rearrangement / 311：
Wallach rearrangement / 312：
Weinreb amide / 313：
Weiss reaction / 314：
Wenker aziridine synthesis / 315：
Wharton oxygen transposition reaction / 316：
Willgerodt-Kindler reaction / 317：
Williamson ether synthesis / 318：
Wittig reaction / 319：
[1,2]-Wittig rearrangement / 320：
[2,3]-Wittig rearrangement / 321：
Wohl-Ziegler reaction / 322：
Wolff rearrangement / 323：
Wolff-Kishner reduction / 324：
Woodward cis-dihydroxylation / 325：
Wurtz reaction / 326：
Yamada coupling reagent / 327：
Yamaguchi esterification / 328：
Zaitsev elimination / 329：
Zincke reaction / 330：
Zinin benzidine rearrangement (semidine rearrangement) / 331：
Subject Index
Abbreviations
Abnormal Claisen rearrangement / 1：
Alder ene reaction / 2：
5.

図書
図書
5. Advanced organic chemistry : reactions and mechanisms. 2nd ed.
Bernard Miller
出版情報: Upper Saddle River, N.J. : Prentice Hall, 2004  xvi, 411 p. ; 25 cm
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Introduction / 1：
Mechanisms of Reactions. Electron Delocalization and Resonance
Electrocyclic Reactions / 2：
Conrotatory and Disrotatory Processes
Explanations for the Woodward-Hoffman Rules
Electrocyclic Reactions with Odd Numbers of Atoms
Photochemical Cyclizations
Cycloaddiction and Cycloreversion Reactions / 3：
Suprafacial and Antarafacial Addition
Selection Rules for Cycloaddition and Cycloreversion Reactions
Examples of Thermal Cycloaddition Reactions
Photochemical Cycloadditions
Sigmatropic Reactions / 4：
Theory of Sigmatropic Shifts
Experimental Observations
Sigmatropic Rearrangements of Charged Systems
Linear Free-Energy Relationships / 5：
The Hammett Equation
Separation of Polar, Resonance, and Steric Effects
Migrations to Electron-Deficient Centers / 6：
Migrations to Electron-Deficient Carbons
The Nature of the Migrating Groups
Rearrangements of Carbocations. Long-Distance Migrations
Migrations to Nitrogen and Oxygen
Neighboring-Group Effects and Nonclassical Cations / 7：
Substitution with Retention of Configuration
Cyclic Halonium Ions
Sulfur and Nitrogen Mustards
Trans/Cis Rate Ratios. Neighboring Acetoxy Groups
Cyclic Phenonium Ions. Double Bonds as Neighboring Groups
Cyclopropane Rings as Neighboring Groups
Neighboring Alkyl Groups: 2-Norbornyl Cations
Rearrangements of Carbanions and Free Radicals / 8：
Carbanion Rearrangements
Rearrangements of Free Radicals
Carbenes, Carbenoids, and Nitrenes / 9：
Formation of Carbenes and Nitrenes
Singlet and Triplet Carbenes. Additions to Double Bonds
Insertion Reactions. Rearrangements
Six-Membered Heterocyclic Rings / 10：
Aromatic Heterocyclic Molecules
Reactions of Pyridine and Its Analogs
Synthesis of Six-Membered Heterocyclic Rings
Five-Membered Heterocyclic Rings / 11：
Electron Delocalization and Aromaticity
Reactions of Five-Membered Heterocyclic Rings
Synthesis of Five-Membered Heteroaromatic Rings
Index
Introduction / 1：
Mechanisms of Reactions. Electron Delocalization and Resonance
Electrocyclic Reactions / 2：
6.

図書
図書
6. Organic chemistry. 8th ed (: pbk)
T.W. Graham Solomons, Craig B. Fryhle
出版情報: Hoboken, N.J. : Wiley, c2004  xxxii, 1255, 8, 14, 4, 27 p. ; 26 cm.
シリーズ名: Wiley international editions
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目次情報: 続きを見る
Carbon Compounds and Chemical Bonds / Chapter 1：
Representative Carbon Compounds: Functional Groups, Intermolecular Forces, and Infrared (IR) Spectroscopy / Chapter 2：
An Introduction to Organic Reactions: Acids and Bases / Chapter 3：
Alkanes: Nomenclature, Conformational Analysis, and an Introduction to Synthesis / Chapter 4：
Stereochemistry: Chiral Molecules / Chapter 5：
Ionic Reactions-Nucleophilic Substitution and Elimination Reactions of Alkyl Halides / Chapter 6：
Alkenes and Alkynes I: Properties and Synthesis, Elimination Reactions of Alkyl Halides / Chapter 7：
Alkenes and Alkynes II: Addition Reactions / Chapter 8：
Nuclear Magnetic Resonance and Mass Spectrometry: Tools for Structure Determination / Chapter 9：
Radical Reactions / Chapter 10：
Alcohols and Ethers / Chapter 11：
Alcohols from Carbonyl Compounds / Chapter 12：
Oxidation-Reduction and Organometallic Compounds
Conjugated Unsaturated Systems / Chapter 13：
Aromatic Compounds / Chapter 14：
Reactions of Aromatic Compounds / Chapter 15：
Aldehydes and Ketones I: Nucleoph ilic Addition to the Carbonyl Group / Chapter 16：
Aldehydes and Ketones II: Aldol Reactions / Chapter 17：
Carboxylic Acids and Their Derivatives / Chapter 18：
Nucleophilic Addition-Elimination at the Acyl Carbon
Synthesis and Reactions of ?-Dicarbonyl Compounds: More Chemistry of Enolate Ions / Chapter 19：
Amines / Chapter 20：
Phenols and Aryl Halides: Nucleophilic Aromatic Substitution / Chapter 21：
Carbohydrates / Chapter 22：
Lipids / Chapter 23：
Amino Acids and Proteins / Chapter 24：
Nucleic Acids and Protein Synthesis / Chapter 25：
Answers to Selected Problems
Glossary
Photo and Illustration Credits
Index
Carbon Compounds and Chemical Bonds / Chapter 1：
Representative Carbon Compounds: Functional Groups, Intermolecular Forces, and Infrared (IR) Spectroscopy / Chapter 2：
An Introduction to Organic Reactions: Acids and Bases / Chapter 3：
7.

図書
図書
7. Dean's handbook of organic chemistry. 2nd ed. / George Gokel
Gokel, George W., 1946- ; Dean, John Aurie, 1921-
出版情報: New York : McGraw-Hill Education , London : McGraw-Hill[m], 2003  800 p ; 23cm
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8.

図書
図書
8. Structure and mechanisms. 4th ed (: hard ; : pbk)
Francis A. Carey and Richard J. Sundberg
出版情報: New York : Kluwer Academic/Plenum Publishers, c2000  xii, 823 p. ; 26 cm
シリーズ名: Advanced organic chemistry / Francis A. Carey and Richard J. Sundberg ; pt. A
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目次情報: 続きを見る
Chemical Bonding and Structure / Chapter 1.：
Valence Bond Description of Chemical Bonding / 1.1.：
Orbital Hybridization / 1.1.1.：
Resonance / 1.1.2.：
Bond Energy, Polarity, and Polarizability / 1.2.：
Bond Energies / 1.2.1.：
Electronegativity and Polarity / 1.2.2.：
Polarizability--Hardness and Softness / 1.2.3.：
Molecular Orbital Theory and Methods / 1.3.：
Huckel Molecular Orbital Theory / 1.4.：
Qualitative Application of Molecular Orbital Theory / 1.5.：
Application of Molecular Orbital Theory to Reactivity / 1.6.：
Interactions between [sigma] and [pi] Systems--Hyperconjugation / 1.7.：
Other Quantitative Descriptions of Molecular Structure / 1.8.：
Atoms in Molecules / 1.8.1.：
Electron Density Functionals / 1.8.2.：
Modern Valence Bond Approaches / 1.8.3.：
General References
Problems
Principles of Stereochemistry / Chapter 2.：
Enantiomeric Relationships / 2.1.：
Diastereomeric Relationships / 2.2.：
Stereochemistry of Reactions / 2.3.：
Prochiral Relationships / 2.4.：
Conformational, Steric, and Stereoelectronic Effects / Chapter 3.：
Strain and Molecular Mechanics / 3.1.：
Conformations of Acyclic Molecules / 3.2.：
Conformations of Cyclohexane Derivatives / 3.3.：
Carbocyclic Rings Other Than Six-Membered / 3.4.：
The Effect of Heteroatoms on Conformational Equilibria / 3.5.：
The Anomeric Effect / 3.6.：
Conformational Effects on Reactivity / 3.7.：
Angle Strain and Its Effect on Reactivity / 3.8.：
Relationships between Ring Size and Rate of Cyclization / 3.9.：
Torsional and Stereoelectronic Effects on Reactivity / 3.10.：
Study and Description of Organic Reaction Mechanismns / Chapter 4.：
Thermodynamic Data / 4.1.：
Kinetic Data / 4.2.：
Substituent Effects and Linear Free-Energy Relationships / 4.3.：
Basic Mechanistic Concepts: Kinetic versus Thermodynamic Control, Hammond's Postulate, the Curtin-Hammett Principle / 4.4.：
Kinetic versus Thermodynamic Control / 4.4.1.：
Hammond's Postulate / 4.4.2.：
The Curtin-Hammett Principle / 4.4.3.：
Isotope Effects / 4.5.：
Isotopes in Labeling Experiments / 4.6.：
Characterization of Reaction Intermediates / 4.7.：
Catalysis by Bronsted Acids and Bases / 4.8.：
Lewis Acid Catalysis / 4.9.：
Solvent Effects / 4.10.：
Substituent Effects in the Gas Phase / 4.11.：
Stereochemistry / 4.12.：
Conclusion / 4.13.：
Nucleophilic Substitution / Chapter 5.：
The Limiting Cases--Substitution by the Ionization (S[subscript N]1) Mechanism / 5.1.：
The Limiting Cases--Substitution by the Direct Displacement (S[subscript N]2) Mechanism / 5.2.：
Detailed Mechanistic Description and Borderline Mechanisms / 5.3.：
Carbocations / 5.4.：
Nucleophilicity and Solvent Effects / 5.5.：
Leaving-Group Effects / 5.6.：
Steric and Strain Effects on Substitution and Ionization Rates / 5.7.：
Effects of Conjugation on Reactivity / 5.8.：
Stereochemistry of Nucleophilic Substitution / 5.9.：
Neighboring-Group Participation / 5.10.：
Mechanism of Rearrangements of Carbocations / 5.11.：
The Norbornyl Cation and Other Nonclassical Carbocations / 5.12.：
Polar Addition and Elimination Reactions / Chapter 6.：
Addition of Hydrogen Halides to Alkenes / 6.1.：
Acid-Catalyzed Hydration and Related Addition Reactions / 6.2.：
Addition of Halogens / 6.3.：
Electrophilic Additions Involving Metal Ions / 6.4.：
Additions to Alkynes and Allenes / 6.5.：
The E2, E1, and E1cb Mechanisms / 6.6.：
Regiochemistry of Elimination Reactions / 6.7.：
Stereochemistry of E2 Elimination Reactions / 6.8.：
Dehydration of Alcohols / 6.9.：
Eliminations Not Involving C--H Bonds / 6.10.：
Carbanions and Other Nucleophilic Carbon Species / Chapter 7.：
Acidity of Hydrocarbons / 7.1.：
Carbanions Stabilized by Functional Groups / 7.2.：
Enols and Enamines / 7.3.：
Carbanions as Nucleophiles in S[subscript N]2 Reactions / 7.4.：
Reactions of Carbonyl Compounds / Chapter 8.：
Hydration and Addition of Alcohols to Aldehydes and Ketones / 8.1.：
Addition-Elimination Reactions of Ketones and Aldehydes / 8.2.：
Addition of Carbon Nucleophiles to Carbonyl Groups / 8.3.：
Reactivity of Carbonyl Compounds toward Addition / 8.4.：
Ester Hydrolysis / 8.5.：
Aminolysis of Esters / 8.6.：
Amide Hydrolysis / 8.7.：
Acylation of Nucleophilic Oxygen and nitrogen Groups / 8.8.：
Intramolecular Catalysis / 8.9.：
Aromaticity / Chapter 9.：
The Concept of Aromaticity / 9.1.：
The Annulenes / 9.2.：
Aromaticity in Charged Rings / 9.3.：
Homoaromaticity / 9.4.：
Fused-Ring Systems / 9.5.：
Heterocyclic Rings / 9.6.：
Aromatic Substitution / Chapter 10.：
Electrophilic Aromatic Substitution Reactions / 10.1.：
Structure-Reactivity Relationships / 10.2.：
Reactivity of Polycyclic and Heteroaromatic Compounds / 10.3.：
Specific Substitution Mechanisms / 10.4.：
Nitration / 10.4.1.：
Halogenation / 10.4.2.：
Protonation and Hydrogen Exchange / 10.4.3.：
Friedel-Crafts Alkylation and Related Reactions / 10.4.4.：
Friedel-Crafts Acylation and Related Reactions / 10.4.5.：
Coupling with Diazonium Compounds / 10.4.6.：
Substitution of Groups Other Than Hydrogen / 10.4.7.：
Nucleophilic Aromatic Substitution by the Addition-Elimination Mechanism / 10.5.：
Nucleophilic Aromatic Substitution by the Elimination-Addition Mechanism / 10.6.：
Concerted Pericyclic Reactions / Chapter 11.：
Electrocyclic Reactions / 11.1.：
Sigmatropic Rearrangements / 11.2.：
Cycloaddition Reactions / 11.3.：
Free-Radical Reactions / Chapter 12.：
Generation and Characterization of Free Radicals / 12.1.：
Background / 12.1.1.：
Stable and Persistent Free Radicals / 12.1.2.：
Direct Detection of Radical Intermediates / 12.1.3.：
Sources of Free Radicals / 12.1.4.：
Structural and Stereochemical Properties of Radical Intermediates / 12.1.5.：
Charged Radical Species / 12.1.6.：
Characteristics of Reaction Mechanisms Involving Radical Intermediates / 12.2.：
Kinetic Characteristics of Chain Reactions / 12.2.1.：
Free-Radical Substitution Reactions / 12.2.2.：
Oxidation / 12.3.1.：
Free-Radical Addition Reactions / 12.4.：
Addition of Hydrogen Halides / 12.4.1.：
Addition of Halomethanes / 12.4.2.：
Addition of Other Carbon Radicals / 12.4.3.：
Addition of Thiols and Thiocarboxylic Acids / 12.4.4.：
Halogen, Sulfur, and Selenium Group Transfer Reactions / 12.5.：
Intramolecular Free-Radical Reactions / 12.6.：
Rearrangement and Fragmentation Reactions of Free Radicals / 12.7.：
Rearrangement Reactions / 12.7.1.：
Fragmentation / 12.7.2.：
Electron-Transfer Reactions Involving Transition-Metal Ions / 12.8.：
S[subscript RN]1 Substitution Processes / 12.9.：
Photochemistry / Chapter 13.：
General Principles / 13.1.：
Orbital Symmetry Considerations Related to Photochemical Reactions / 13.2.：
Photochemistry of Carbonyl Compounds / 13.3.：
Photochemistry of Alkenes and Dienes / 13.4.：
Photochemistry of Aromatic Compounds / 13.5.：
References to Problems
Index
Chemical Bonding and Structure / Chapter 1.：
Valence Bond Description of Chemical Bonding / 1.1.：
Orbital Hybridization / 1.1.1.：
9.

図書
図書
9. Organic spectroscopy : principles and applications
Jag Mohan
出版情報: New Delhi : Narosa, 2001, c2000  viii, 512 p. ; 23 cm
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10.

図書
図書
10. Reactions and synthesis. 4th ed (: hard ; : pbk)
Francis A. Carey and Richard J. Sundberg
出版情報: New York : Kluwer Academic/Plenum Publishers, c2001  xii, 965 p. ; 26 cm
シリーズ名: Advanced organic chemistry / Francis A. Carey and Richard J. Sundberg ; pt. B
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目次情報: 続きを見る
Alkylation of Nucleophilic Carbon Intermediates / Chapter 1.：
Generation of Carbanions by Deprotonation / 1.1.：
Regioselectivity and Stereoselectivity in Enolate Formation / 1.2.：
Other Means of Generating Enolates / 1.3.：
Alkylation of Enolates / 1.4.：
Generation and Alkylation of Dianions / 1.5.：
Medium Effects in the Alkylation of Enolates / 1.6.：
Oxygen versus Carbon as the Site of Alkylation / 1.7.：
Alkylation of Aldehydes, Esters, Amides, and Nitriles / 1.8.：
The Nitrogen Analogs of Enols and Enolates--Enamines and Imine Anions / 1.9.：
Alkylation of Carbon Nucleophiles by Conjugate Addition / 1.10.：
General References
Problems
Reaction of Carbon Nucleophiles with Carbonyl Groups / Chapter 2.：
Aldol Addition and Condensation Reactions / 2.1.：
The General Mechanism / 2.1.1.：
Mixed Aldol Condensations with Aromatic Aldehydes / 2.1.2.：
Control of Regiochemistry and Stereochemistry of Mixed Aldol Reactions of Aliphatic Aldehydes and Ketones / 2.1.3.：
Intramolecular Aldol Reactions and the Robinson Annulation / 2.1.4.：
Addition Reactions of Imines and Iminium Ions / 2.2.：
The Mannich Reaction / 2.2.1.：
Amine-Catalyzed Condensation Reactions / 2.2.2.：
Acylation of Carbanions / 2.3.：
The Wittig and Related Reactions of Phosphorus-Stabilized Carbon Nucleophiles / 2.4.：
Reactions of Carbonyl Compounds with [alpha]-Trimethylsilylcarbanions / 2.5.：
Sulfur Ylides and Related Nucleophiles / 2.6.：
Nucleophilic Addition--Cyclization / 2.7.：
Functional Group Interconversion by Nucleophilic Substitution / Chapter 3.：
Conversion of Alcohols to Alkylating Agents / 3.1.：
Sulfonate Esters / 3.1.1.：
Halides / 3.1.2.：
Introduction of Functional Groups by Nucleophilic Substitution at Saturated Carbon / 3.2.：
General Solvent Effects / 3.2.1.：
Nitriles / 3.2.2.：
Azides / 3.2.3.：
Oxygen Nucleophiles / 3.2.4.：
Nitrogen Nucleophiles / 3.2.5.：
Sulfur Nucleophiles / 3.2.6.：
Phosphorus Nucleophiles / 3.2.7.：
Summary of Nucleophilic Substitution at Saturated Carbon / 3.2.8.：
Nucleophilic Cleavage of Carbon-Oxygen Bonds in Ethers and Esters / 3.3.：
Interconversion of Carboxylic Acid Derivatives / 3.4.：
Preparation of Reactive Reagents for Acylation / 3.4.1.：
Preparation of Esters / 3.4.2.：
Preparation of Amides / 3.4.3.：
Electrophilic Additions to Carbon--Carbon Multiple Bonds / Chapter 4.：
Addition of Hydrogen Halides / 4.1.：
Hydration and Other Acid-Catalyzed Additions of Oxygen Nucleophiles / 4.2.：
Oxymercuration / 4.3.：
Addition of Halogens to Alkenes / 4.4.：
Electrophilic Sulfur and Selenium Reagents / 4.5.：
Addition of Other Electrophilic Reagents / 4.6.：
Electrophilic Substitution Alpha to Carbonyl Groups / 4.7.：
Additions to Allenes and Alkynes / 4.8.：
Addition at Double Bonds via Organoborane Intermediates / 4.9.：
Hydroboration / 4.9.1.：
Reactions of Organoboranes / 4.9.2.：
Enantioselective Hydroboration / 4.9.3.：
Hydroboration of Alkynes / 4.9.4.：
Reduction of Carbonyl and Other Functional Groups / Chapter 5.：
Addition of Hydrogen / 5.1.：
Catalytic Hydrogenation / 5.1.1.：
Other Hydrogen-Transfer Reagents / 5.1.2.：
Group III Hydride-Donor Reagents / 5.2.：
Reduction of Carbonyl Compounds / 5.2.1.：
Stereoselectivity of Hydride Reduction / 5.2.2.：
Reduction of Other Functional Groups by Hydride Donors / 5.2.3.：
Group IV Hydride Donors / 5.3.：
Hydrogen-Atom Donors / 5.4.：
Dissolving-Metal Reductions / 5.5.：
Reductive Removal of Functional Groups / 5.5.1.：
Reductive Carbon--Carbon Bond Formation / 5.5.3.：
Reductive Deoxygenation of Carbonyl Groups / 5.6.：
Reductive Elimination and Fragmentation / 5.7.：
Cycloadditions, Unimolecular Rearrangements, and Thermal Eliminations / Chapter 6.：
Cycloaddition Reactions / 6.1.：
The Diels--Alder Reaction: General Features / 6.1.1.：
The Diels--Alder Reaction: Dienophiles / 6.1.2.：
The Diels--Alder Reaction: Dienes / 6.1.3.：
Asymmetric Diels--Alder Reactions / 6.1.4.：
Intramolecular Diels--Alder Reactions / 6.1.5.：
Dipolar Cycloaddition Reactions / 6.2.：
[2 + 2] Cycloadditions and Other Reactions Leading to Cyclobutanes / 6.3.：
Photochemical Cycloaddition Reactions / 6.4.：
[3,3] Sigmatropic Rearrangements / 6.5.：
Cope Rearrangements / 6.5.1.：
Claisen Rearrangements / 6.5.2.：
[2,3] Sigmatropic Rearrangements / 6.6.：
Ene Reactions / 6.7.：
Unimolecular Thermal Elimination Reactions / 6.8.：
Cheletropic Elimination / 6.8.1.：
Decomposition of Cyclic Azo Compounds / 6.8.2.：
[beta] Eliminations Involving Cyclic Transition States / 6.8.3.：
Organometallic Compounds of the Group I, II, and III Metals / Chapter 7.：
Preparation and Properties / 7.1.：
Reactions of Organomagnesium and Organolithium Compounds / 7.2.：
Reactions with Alkylating Agents / 7.2.1.：
Reactions with Carbonyl Compounds / 7.2.2.：
Organic Derivatives of Group IIB and Group IIIB Metals / 7.3.：
Organozinc Compounds / 7.3.1.：
Organocadmium Compounds / 7.3.2.：
Organomercury Compounds / 7.3.3.：
Organoindium Reagents / 7.3.4.：
Organolanthanide Reagents / 7.4.：
Reactions Involving the Transition Metals / Chapter 8.：
Organocopper Intermediates / 8.1.：
Preparation and Structure of Organocopper Reagents / 8.1.1.：
Reactions Involving Organocopper Reagents and Intermediates / 8.1.2.：
Reactions Involving Organopalladium Intermediates / 8.2.：
Palladium-Catalyzed Nucleophilic Substitution and Alkylation / 8.2.1.：
The Heck Reaction / 8.2.2.：
Palladium-Catalyzed Cross Coupling / 8.2.3.：
Carbonylation Reactions / 8.2.4.：
Reactions Involving Organonickel Compounds / 8.3.：
Reactions Involving Rhodium and Cobalt / 8.4.：
Organometallic Compounds with [pi] Bonding / 8.5.：
Carbon--Carbon Bond-Forming Reactions of Compounds of Boron, Silicon, and Tin / Chapter 9.：
Organoboron Compounds / 9.1.：
Synthesis of Organoboranes / 9.1.1.：
Carbon--Carbon Bond-Forming Reactions of Organoboranes / 9.1.2.：
Organosilicon Compounds / 9.2.：
Synthesis of Organosilanes / 9.2.1.：
Carbon--Carbon Bond-Forming Reactions / 9.2.2.：
Organotin Compounds / 9.3.：
Synthesis of Organostannanes / 9.3.1.：
Reactions Involving Carbocations, Carbenes, and Radicals as Reactive Intermediates / 9.3.2.：
Reactions Involving Carbocation Intermediates / 10.1.：
Carbon-Carbon Bond Formation Involving Carbocations / 10.1.1.：
Rearrangement of Carbocations / 10.1.2.：
Related Rearrangements / 10.1.3.：
Fragmentation Reactions / 10.1.4.：
Reactions Involving Carbenes and Nitrenes / 10.2.：
Structure and Reactivity of Carbenes / 10.2.1.：
Generation of Carbenes / 10.2.2.：
Addition Reactions / 10.2.3.：
Insertion Reactions / 10.2.4.：
Generation and Reactions of Ylides by Carbenoid Decomposition / 10.2.5.：
Rearrangement Reactions / 10.2.6.：
Related Reactions / 10.2.7.：
Nitrenes and Related Intermediates / 10.2.8.：
Rearrangements to Electron-Deficient Nitrogen / 10.2.9.：
Reactions Involving Free-Radical Intermediates / 10.3.：
Sources of Radical Intermediates / 10.3.1.：
Introduction of Functionality by Radical Reactions / 10.3.2.：
Addition Reactions of Radicals to Substituted Alkenes / 10.3.3.：
Cyclization of Free-Radical Intermediates / 10.3.4.：
Fragmentation and Rearrangement Reactions / 10.3.5.：
Aromatic Substitution Reactions / Chapter 11.：
Electrophilic Aromatic Substitution / 11.1.：
Nitration / 11.1.1.：
Halogenation / 11.1.2.：
Friedel-Crafts Alkylations and Acylations / 11.1.3.：
Electrophilic Metalation / 11.1.4.：
Nucleophilic Aromatic Substitution / 11.2.：
Aryl Diazonium Ions as Synthetic Intermediates / 11.2.1.：
Substitution by the Addition-Elimination Mechanism / 11.2.2.：
Substitution by the Elimination-Addition Mechanism / 11.2.3.：
Transition-Metal-Catalyzed Substitution Reactions / 11.2.4.：
Aromatic Radical Substitution Reactions / 11.3.：
Substitution by the S[subscript RN]1 Mechanism / 11.4.：
Oxidations / Chapter 12.：
Oxidation of Alcohols to Aldehydes, Ketones, or Carboxylic Acids / 12.1.：
Transition-Metal Oxidants / 12.1.1.：
Other Oxidants / 12.1.2.：
Addition of Oxygen at Carbon-Carbon Double Bonds / 12.2.：
Epoxides from Alkenes and Peroxidic Reagents / 12.2.1.：
Transformations of Epoxides / 12.2.3.：
Reaction of Alkenes with Singlet Oxygen / 12.2.4.：
Cleavage of Carbon-Carbon Double Bonds / 12.3.：
Oxonolysis / 12.3.1.：
Selective Oxidative Cleavages at Other Functional Groups / 12.4.：
Cleavage of Glycols / 12.4.1.：
Oxidative Decarboxylation / 12.4.2.：
Oxidation of Ketones and Aldehydes / 12.5.：
Oxidation of Ketones and Aldehydes by Oxygen and Peroxidic Compounds / 12.5.1.：
Oxidation with Other Reagents / 12.5.3.：
Allylic Oxidation / 12.6.：
Oxidations at Unfunctionalized Carbon / 12.6.1.：
Planning and Execution of Multistep Syntheses / Chapter 13.：
Protective Groups / 13.1.：
Hydroxyl-Protecting Groups / 13.1.1.：
Amino-Protecting Groups / 13.1.2.：
Carbonyl-Protecting Groups / 13.1.3.：
Carboxylic Acid-Protecting Groups / 13.1.4.：
Synthetic Equivalent Groups / 13.2.：
Synthetic Analysis and Planning / 13.3.：
Control of Stereochemistry / 13.4.：
Illustrative Syntheses / 13.5.：
Juvabione / 13.5.1.：
Longifolene / 13.5.2.：
Prelog-Djerassi Lactone / 13.5.3.：
Taxol / 13.5.4.：
Epothilone A / 13.5.5.：
Solid-Phase Synthesis / 13.6.：
Solid-Phase Synthesis of Polypeptides / 13.6.1.：
Solid-Phase Synthesis of Oligonucleotides / 13.6.2.：
Combinatorial Synthesis / 13.7.：
References for Problems
Index
Alkylation of Nucleophilic Carbon Intermediates / Chapter 1.：
Generation of Carbanions by Deprotonation / 1.1.：
Regioselectivity and Stereoselectivity in Enolate Formation / 1.2.：
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