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1.

図書

図書
Jag Mohan
出版情報: New Delhi : Narosa, 2001, c2000  viii, 512 p. ; 23 cm
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2.

図書

図書
Kin-ya Akiba
出版情報: Hoboken, N.J. : Wiley, c2011  xi, 275 p. ; 24 cm
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3.

図書

図書
T.W. Graham Solomons, Craig B. Fryhle
出版情報: Hoboken, N.J. : John Wiley & Sons, c2011  xxxiii, 1164, 9, 22, 21 p. ; 28 cm
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The Basics: Bonding And Molecular Structure / 1:
Families Of Carbon Compounds: Functional Groups, Intermolecular Forces, And Infrared (Ir) Spectroscopy / 2:
An Introduction To Organic Reactions And Their Mechanisms: Acids And Bases / 3:
Nomenclature And Conformations Of Alkanes And Cycloalkanes / 4:
Stereochemistry: Chiral Molecules / 5:
Ionic Reactions: Nucleophilic Substitution And Elimination Reactions Of Alkyl Halides / 6:
Alkenes And Alkynes I: Properties And Synthesis. Elimination Reactions Of Alkyl Halides / 7:
Alkenes And Alkynes Ii: Addition Reactions / 8:
Nuclear Magnetic Resonance And Mass Spectrometry: Tools For Structure Determination / 9:
Radical Reactions / 10:
Alcohols And Ethers / 11:
Alcohols From Carbonyl Compounds: Oxidation-Reduction And Organometallic Compounds / 12:
Answers To Selected Problems
Glossary
Photo Credits
Index
The Basics: Bonding And Molecular Structure / 1:
Families Of Carbon Compounds: Functional Groups, Intermolecular Forces, And Infrared (Ir) Spectroscopy / 2:
An Introduction To Organic Reactions And Their Mechanisms: Acids And Bases / 3:
4.

図書

図書
Jie Jack Li
出版情報: Berlin : Springer, c2006  xx, 652 p. ; 24 cm
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Abbreviations
Alder ene reaction
Aldol condensation / 1:
Abnormal Claisen rearrangement
Algar-Flynn-Oyamada reaction / 2:
Allan-Robinson reaction
Appel reaction / 3:
Arndt-Eistert homologation / 4:
Baeyer-Villiger oxidation
Baker-Venkataraman rearrangement / 5:
Alper carbonylation
Bamberger rearrangement / 6:
Amadori rearrangement
Bamford-Stevens reaction
Barbier coupling reaction / 7:
Angeli-Rimini hydroxamic acid synthesis
Bargellini reaction / 8:
ANRORC mechanism
Bartoli indole synthesis
Barton radical decarboxylation / 9:
Barton-McCombie deoxygenation / 10:
Auwers reaction
Barton nitrite photolysis
Barton-Zard reaction / 11:
Baeyer-Drewson indigo synthesis
Batcho-Leimgruber indole synthesis / 12:
Baylis-Hillman reaction
Beckmann rearrangement / 13:
Beirut reaction / 14:
Benzilic acid rearrangement
Benzoin condensation / 15:
Bergman cyclization / 16:
Biginelli pyrimidone synthesis
Birch reduction / 17:
Bischler-Mohlau indole synthesis / 18:
Barton decarboxylation
Bischler-Napieralski reaction
Blaise reaction / 19:
Blanc chloromethylation / 20:
Blum aziridine synthesis
Boekelheide reaction / 21:
Boger pyridine synthesis / 22:
Borch reductive amination
Borsche-Drechsel cyclization / 23:
Boulton-Katritzky rearrangement / 24:
Bouveault aldehyde synthesis
Bouveault-Blanc reduction / 25:
Boyland-Sims oxidation / 26:
Bradsher reaction
Brook rearrangement / 27:
Brown hydroboration / 28:
Bucherer carbazole synthesis
Bucherer reaction / 29:
Bischler-Möhlau indole synthesis
Bucherer-Bergs reaction / 30:
Buchner-Curtius-Schlotterbeck reaction
Buchner method of ring expansion / 31:
Buchwald-Hartwig C-N bond and C-O bond formation reactions / 32:
Blanc chloromethylation reaction
Burgess dehydrating reagent
Cadiot-Chodkiewicz coupling / 33:
Camps quinolinol synthesis / 34:
Cannizzaro dispropotionation
Carroll rearrangement / 35:
Boord reaction
Castro-Stephens coupling / 36:
Chan alkyne reduction
Chan-Lam coupling reaction / 37:
Chapman rearrangement / 38:
Chichibabin pyridine synthesis
Chugaev reaction / 39:
Ciamician-Dennsted rearrangement / 40:
Claisen condensation
Claisen isoxazole synthesis / 41:
Claisen rearrangement / 42:
Eschenmoser-Claisen amide acetal rearrangement / 43:
Brown hydroboration reaction
Ireland-Claisen (silyl ketene acetal) rearrangement / 44:
Johnson-Claisen (orthoester) rearrangement
Clemmensen reduction / 45:
Combes quinoline synthesis / 46:
Conrad-Limpach reaction
Cope elimination reaction / 47:
Cope rearrangement / 48:
Oxy-Cope rearrangement
Anionic oxy-Cope rearrangement / 49:
Corey-Bakshi-Shibata (CBS) reduction / 50:
Corey-Chaykovsky reaction
Corey-Fuchs reaction / 51:
Corey-Kim oxidation / 52:
Cannizzaro dispropotionation reaction
Corey-Nicolaou macrolactonization
Corey-Seebach dithiane reaction / 53:
Corey-Winter olefin synthesis / 54:
Criegee glycol cleavage
Criegee mechanism of ozonolysis / 55:
Curtius rearrangement / 56:
Chichibabin amination reaction
Dakin oxidation
Dakin-West reaction / 57:
Danheiser annulation / 58:
Darzens glycidic ester condensation
Davis chiral oxaziridine reagent / 59:
Delepine amine synthesis / 60:
de Mayo reaction
Demjanov rearrangement / 61:
Tiffeneau-Demjanov rearrangement / 62:
Clarke-Eschweiler reductive alkylation of amines
Dess-Martin oxidation
Dieckmann condensation / 63:
Diels-Alder reaction / 64:
Dienone-phenol rearrangement
Di-[pi]-methane rearrangement / 65:
Doebner quinoline synthesis / 66:
Cook-Heilbron thiazole synthesis
Dotz reaction
Dowd-Beckwith ring expansion / 67:
Erlenmeyer-Plochl azlactone synthesis / 68:
Cope, oxy-Cope, and anionic oxy-Cope rearrangements
Eschenmoser-Tanabe fragmentation
Eschweiler-Clarke reductive alkylation of amines / 69:
Evans aldol reaction / 70:
Favorskii rearrangement and quasi-Favorskii rearrangement
Feist-Benary furan synthesis / 71:
Ferrier carbocyclization / 72:
Ferrier glycal allylic rearrangement
Fiesselmann thiophene synthesis / 73:
Fischer indole synthesis / 74:
Cornforth rearrangement
Fischer oxazole synthesis
Fleming-Tamao oxidation / 75:
Tamao-Kumada oxidation / 76:
Friedel-Crafts reaction
Friedlander quinoline synthesis / 77:
Fries rearrangement / 78:
Fukuyama amine synthesis
Fukuyama reduction / 79:
Gabriel synthesis / 80:
Ing-Manske procedure
Gabriel-Colman rearrangement / 81:
Gassman indole synthesis / 82:
Gattermann-Koch reaction
Gewald aminothiophene synthesis / 83:
Glaser coupling / 84:
Eglinton coupling
Gomberg-Bachmann reaction / 85:
Dess-Martin periodinane oxidation
Gould-Jacobs reaction / 86:
Grignard reaction
Grob fragmentation / 87:
Guareschi-Thorpe condensation / 88:
Hajos-Wiechert reaction
Haller-Bauer reaction / 89:
Di-?-methane rearrangement
Hantzsch dihydropyridine synthesis / 90:
Doebner reaction
Hantzsch pyrrole synthesis
Heck reaction / 91:
Doebner-von Miller reaction
Heteroaryl Heck reaction / 92:
Doering-LaFlamme allene synthesis
Hegedus indole synthesis
Hell-Volhard-Zelinsky reaction / 93:
Dornow-Wiehler isoxazole synthesis
Henry nitroaldol reaction / 94:
Dötz reaction
Hinsberg synthesis of thiophene derivatives
Hiyama cross-coupling reaction / 95:
Dowd ring expansion
Hiyama-Denmark cross-coupling reaction / 96:
Dutt-Wormall reaction
Hofmann rearrangement
Hofmann-Loffler-Freytag reaction / 97:
Eglinton reaction
Horner-Wadsworth-Emmons reaction / 98:
Eschenmoser coupling reaction
Houben-Hoesch synthesis
Hunsdiecker-Borodin reaction / 99:
Hurd-Mori 1,2,3-thiadiazole synthesis / 100:
Étard reaction
Jacobsen-Katsuki epoxidation
Japp-Klingemann hydrazone synthesis / 101:
Jones oxidation / 102:
Favorskii rearrangement and Quasi-Favorskii rearrangement
Julia-Kocienski olefination
Julia-Lythgoe olefination / 103:
Feist-Bénary furan synthesis
Kahne-Crich glycosidation / 104:
Ferrier rearrangement
Keck macrolactonization
Knoevenagel condensation / 105:
Finkelstein reaction
Knorr pyrazole synthesis / 106:
Fischer-Hepp rearrangement
Paal-Knorr pyrrole synthesis
Koch-Haaf carbonylation / 107:
Koenig-Knorr glycosidation / 108:
Fischer-Speier esterification
Kolbe-Schmitt reaction
Kostanecki reaction / 109:
Fleming oxidation
Krohnke pyridine synthesis / 110:
Forster reaction
Kumada cross-coupling reaction
Lawesson's reagent / 111:
Frater-Seebach alkylation
Leuckart-Wallach reaction / 112:
Lossen rearrangement
McFadyen-Stevens reduction / 113:
Friedländer synthesis
McMurry coupling / 114:
MacMillan catalyst
Mannich reaction / 115:
Fritsch-Buttenberg-Wiechell rearrangement
Marshall boronate fragmentation / 116:
Fujimoto-Belleau reaction
Martin's sulfurane dehydrating reagent
Masamune-Roush conditions / 117:
Meerwein-Ponndorf-Verley reduction / 118:
Meisenheimer complex
[1,2]-Meisenheimer rearrangement / 119:
[2,3]-Meisenheimer rearrangement / 120:
Meth-Cohn quinoline synthesis
Meyers oxazoline method / 121:
Meyer-Schuster rearrangement / 122:
Michael addition
Michaelis-Arbuzov phosphonate synthesis / 123:
Midland reduction / 124:
Gribble indole reduction
Mislow-Evans rearrangement
Mitsunobu reaction / 125:
Gribble reduction of diaryl ketones
Miyaura borylation / 126:
Moffatt oxidation
Montgomery coupling / 127:
Morgan-Walls reaction / 128:
Pictet-Hubert reaction
Mori-Ban indole synthesis / 129:
Mukaiyama aldol reaction / 130:
Mukaiyama Michael addition
Mukaiyama reagent / 131:
Hantzsch pyridine synthesis
Myers-Saito cyclization / 132:
Nazarov cyclization
Neber rearrangement / 133:
Haworth reaction
Nef reaction / 134:
Hayashi rearrangement
Negishi cross-coupling reaction
Nenitzescu indole synthesis / 135:
Nicholas reaction / 136:
Nicolaou dehydrogenation
Nicolaou hydroxy-dithioketal cyclization / 137:
Hell-Volhardt-Zelinsky reaction
Nicolaou hydroxy-ketone reductive cyclic ether formation / 138:
Henry reaction (nitroaldol reaction)
Nicolaou oxyselenation
Noyori asymmetric hydrogenation / 139:
Herz reaction
Nozaki-Hiyama-Kishi reaction / 140:
Oppenauer oxidation
Overman rearrangement / 141:
Paal thiophene synthesis / 142:
Hoch-Campbell aziridine synthesis
Paal-Knorr furan synthesis
Parham cyclization / 143:
Hodges-Vedejs metallation of oxazoles
Passerini reaction / 144:
Hofmann rearrangement (Hofmann degradation reaction)
Paterno-Buchi reaction
Pauson-Khand cyclopentenone synthesis / 145:
Hofmann-Löffler-Freytag reaction
Payne rearrangement / 146:
Hofmann-Martius reaction (Reilly-Hickinbottom rearrangement)
Pechmann coumarin synthesis
Perkin reaction / 147:
Hooker oxidation
Petasis reaction / 148:
Peterson olefination
Pictet-Gams isoquinoline synthesis / 149:
Pictet-Spengler tetrahydroisoquinoline synthesis / 150:
Hunsdiecker reaction
Pinacol rearrangement
Pinner reaction / 151:
Polonovski reaction / 152:
Polonovski-Potier rearrangement
Pomeranz-Fritsch reaction / 153:
Jacobsen rearrangement
Schlittler-Muller modification / 154:
Prevost trans-dihydroxylation
Woodward cis-dihydroxylation / 155:
Prins reaction / 156:
Kahne glycosidation
Pschorr cyclization
Pummerer rearrangement / 157:
Keck stereoselective allylation
Ramberg-Backlund reaction / 158:
Reformatsky reaction
Regitz diazo synthesis / 159:
Kemp elimination
Reimer-Tiemann reaction / 160:
Kennedy oxidative cyclization
Reissert aldehyde synthesis
Reissert indole synthesis / 161:
Kharasch addition reaction
Ring-closing metathesis / 162:
Ritter reaction
Robinson annulation / 163:
Knorr pyrrole synthesis
Robinson-Gabriel synthesis / 164:
Koch carbonylation reaction (Koch-Haaf carbonylation reaction)
Robinson-Schopf reaction
Rosenmund reduction / 165:
Rubottom oxidation / 166:
Kolbe electrolytic coupling
Rupe rearrangement
Saegusa oxidation / 167:
Sakurai allylation reaction / 168:
Sandmeyer reaction
Schiemann reaction / 169:
Krapcho decarboxylation
Schmidt reaction / 170:
Kröhnke reaction (pyridine synthesis)
Schmidt's trichloroacetimidate glycosidation reaction
Shapiro reaction / 171:
Sharpless asymmetric amino hydroxylation / 172:
Larock indole synthesis
Sharpless asymmetric epoxidation
Sharpless asymmetric dihydroxylation / 173:
Sharpless olefin synthesis / 174:
Simmons-Smith reaction
Skraup quinoline synthesis / 175:
Lieben haloform reaction
Liebeskind-Srogl coupling / 176:
Smiles rearrangement
Newman-Kwart reaction / 177:
Truce-Smile rearrangement / 178:
Luche reduction
Sommelet reaction
Sommelet-Hauser rearrangement / 179:
Sonogashira reaction / 180:
McLafferty rearrangement
Staudinger ketene cycloaddition
Staudinger reduction / 181:
Stembach benzodiazepine synthesis / 182:
Madelung indole synthesis
Stetter reaction
Still-Gennari phosphonate reaction / 183:
Stille coupling / 184:
Stille-Kelly reaction
Stobbe condensation / 185:
Stork enamine reaction / 186:
Strecker amino acid synthesis
Suzuki coupling / 187:
Meerwein arylation
Swern oxidation / 188:
Takai iodoalkene synthesis
Tebbe olefination / 189:
Meinwald rearrangement
Petasis alkenylation / 190:
TEMPO-mediated oxidation
Thorpe-Ziegler reaction / 191:
Meisenheimer rearrangement
Tsuji-Trost allylation / 192:
Ugi reaction
Ullmann reaction / 193:
van Leusen oxazole synthesis / 194:
Vilsmeier-Haack reaction
Vilsmeier mechanism for acid chloride formation / 195:
Vinylcyclopropane-cyclopentene rearrangement / 196:
Miller-Loudon-Snyder nitrile synthesis
von Braun reaction
Wacker oxidation / 197:
Wagner-Meerwein rearrangement / 198:
Weiss-Cook reaction
Wharton oxygen transposition reaction / 199:
Miyaura boration reaction
Willgerodt-Kindler reaction / 200:
Wittig reaction
Schlosser modification of the Wittig reaction / 201:
Morgan-Walls reaction (Pictet-Hubert reaction)
[1,2]-Wittig rearrangement / 202:
[2,3]-Wittig rearrangement
Wohl-Ziegler reaction / 203:
Morin rearrangement
Wolff rearrangement / 204:
Wolff-Kishner reduction
Yamaguchi esterification / 205:
Mukaiyama esterification
Zincke reaction / 206:
Subject Index
Nametkin rearrangement (retropinacol rearrangement) / 207:
Orton rearrangement / 208:
Paterno-Büchi reaction / 218:
Pechmann condensation (coumarin synthesis) / 224:
Pechmann pyrazole synthesis / 227:
Perkin reaction (cinnamic acid synthesis) / 228:
Perkow vinyl phosphate synthesis / 229:
Pfau-Plattner azulene synthesis / 230:
Pfitzinger quinoline synthesis / 232:
Pinner synthesis / 233:
Prévost trans-dihydroxylation / 237:
Prilezhaev reaction / 241:
Pschorr ring closure / 242:
Ramberg-Bäcklund olefin synthesis / 244:
Reissert reaction (aldehyde synthesis) / 246:
Riley oxidation (selenium dioxide oxidation) / 250:
Ring-closing metathesis (RCM) using Grubbs and Schrock catalysts / 251:
Robinson-Schöpf reaction / 252:
Roush allylboronate reagent / 255:
Rychnovsky polyol synthesis / 257:
Sakurai allylation reaction (Hosomi-Sakurai reaction) / 260:
Sarett oxidation / 261:
Schiemann reaction (Balz-Schiemann reaction) / 263:
Scholl reaction / 264:
Schöpf reaction / 268:
Schotten-Baumann reaction / 269:
Sharpless dihydroxylation / 270:
Shi asymmetric epoxidation / 274:
Simonini reaction / 275:
Simonis chromone cyclization / 277:
Sommelet-Hauser (ammonium ylide) rearrangement / 278:
Staudinger reaction / 282:
Stetter reaction (Michael-Stetter reaction) / 284:
Stevens rearrangement / 285:
Stieglitz rearrangement / 286:
Stollé synthesis / 287:
Tebbe olefination (Petasis alkenylation) / 292:
Tiemann rearrangement / 298:
Tishchenko reaction / 300:
Tollens reaction / 302:
Ueno-Stork cyclization / 303:
von Richter reaction / 305:
Wallach rearrangement / 310:
Weinreb amide / 313:
Weiss reaction / 314:
Wenker aziridine synthesis / 315:
Williamson ether synthesis / 316:
Wurtz reaction / 319:
Yamada coupling reagent / 327:
Zaitsev elimination / 328:
Zinin benzidine rearrangement (semidine rearrangement) / 330:
Abbreviations
Alder ene reaction
Aldol condensation / 1:
5.

図書

図書
edited by Raphael Ikan
出版情報: Singapore ; Hackensack, N.J. : World Scientific, c2008  xix, 604 p. ; 24 cm
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Preface
Acknowledgments
Contributors
The Origin and the Nature of Natural Products / Raphael IkanChapter 1:
Plant-Derived Natural Products in Drug Discovery and Development: An Overview / Mark Bahar ; Ye Deng ; Joshua N. Fletcher ; A. Douglas KinghornChapter 2:
Plant and Brain Cannabinoids: The Chemistry of Major New Players in Physiology / Lumir Hanus ; Raphael MechoulamChapter 3:
Natural Products as Biomarker Tracers in Environmental and Geological Processes / Bernd R. T. SimoneitChapter 4:
Toxins of Marine Invertebrates and Microorganisms / Yoel Kashman ; Yehuda BenayahuChapter 5:
Enantiomeric Distribution of Odorous Oxygenated Monoterpenes in Aromatic Plants / Uzi RavidChapter 6:
Recent Trends of Some Natural Sweet Substances from Plants / Bernard CrammerChapter 7:
Natural Products for Pest Management / Stephen O. Duke ; Agnes M. Rimando ; Kevin K. Schrader ; Charles Cantrell ; Kumudini M. Meepagala ; David E. Wedge ; Nurhayat Tabanca ; Franck E. DayanChapter 8:
Natural Products in Mycelial Microorganisms: Impact of Morphology / Sergei BraunChapter 9:
Recent Advances in the Chemistry of Insect Pheromones / Mangesh J. Goundalkar ; Francis X. WebsterChapter 10:
Nature Derived Antibiotics / Srinivas Kodali ; Jun WangChapter 11:
Natural Products and Related Compounds of Realized and Potential Use in Treating Neurodegenerative Disease / Peter J. Houghton ; Melanie-Jayne HowesChapter 12:
Phytotoxic Compounds with Calmodulin Inhibitor Properties from Selected Mexican Fungi and Plants / Rachel Mata ; Sergio-Martinez Luis ; Araceli Perez-VasquesChapter 13:
Potential Anticancer Natural Products from Plant-Associated Fungi / Marilyn T. Marron ; A. A. Leslie GunatilakaChapter 14:
Plant Fungal Endophytes: Interactions, Metabolites and Biosyntheses / John R. PorterChapter 15:
Index
Preface
Acknowledgments
Contributors
6.

図書

図書
Michael B. Smith, Jerry March
出版情報: New York : John Wiley, 2001  xviii, 2083 p. ; 24 cm
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Preface
Biographical Note
Abbreviations
Localized Chemical Bonding / Part 1:
Delocalized Chemical Bonding / Chapter 2:
Bonding Weaker than Covalent / Chapter 3:
Stereochemistry / Chapter 4:
Carbocations, Carbanions, Free Radicals, Carbenes, and Nitrenes / Chapter 5:
Mechanisms and Methods of Determining Them / Chapter 6:
Irradiation Processes in Organic Chemistry / Chapter 7:
Acids and Bases / Chapter 8:
Effects of Structure on Reactivity / Chapter 9:
Aliphatic Substitution: Nucleophilic and Organometallic / Part 2:
Aromatic Substituion, Electrophilic / Chapter 11:
Aliphatic, Alkenyl, and Alkynyl Substitution, Electrophilic and Organometallic / Chapter 12:
Aromatic Substitution, Nucleophilic and Organometallic / Chapter 13:
Substitution Reactions: Free Radicals / Chapter 14:
Addition to Carbon-Carbon Multiple Bonds / Chapter 15:
Addition to Carbon-Hetero Multiple Bonds / Chapter 16:
Eliminations / Chapter 17:
Rearrangements / Chapter 18:
Oxidations and Reductions / Chapter 19:
The Literature of Organic Chemistry / Appendix A:
Classification of Reactions by Type of Compound Synthesized / Appendix B:
Indexes
Author Index
Subject Index
Preface
Biographical Note
Abbreviations
7.

図書

図書
T.W. Graham Solomons
出版情報: New York : John Wiley & Sons, c1996  xxvii, 1218, 10, 19, 43 p. ; 26 cm
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Carbon Compounds and Chemical Bonds / 1:
Representative Carbon Compounds: Functional Groups, Infrared Spectroscopy, & Intermolecular Force / 2:
An Introduction to Organic Reactions: Acids and Bases / 3:
Alkanes: Nomenclature, Conformational Analysis, & An Intro to Synthesis / 4:
Stereochemistry: Chiral Molecules / 5:
Ionic Reactions - Nucleophilic Substitution & Elimination Reactions: Alkyl Halides / 6:
Alkenes & Alkynes: Properties & Synthesis, Elimination Reactions of Alkyl Halides / 7:
Alkenes & Alkynes II: Addition Reaction / 8:
Spectroscopic Methods of Structure Determination / 9:
Radical Reactions / 10:
Alcohols & Ethers / 11:
Alcohols from Carbonyl Compounds, Oxidation-Reduction & Organometallic Compounds / 12:
Conjugated Unsaturated Systems / 13:
Aromatic Compounds / 14:
Reactions of Aromatic Compounds / 15:
Aldehydes & Ketones I: Nucleophilic Additions to the Carbonyl Group / 16:
Aldehydes & Ketones II: Enolates & Enols / 17:
Aldol & Alkylation Reactions
Carboxylic Acids & Their Derivatives: Nucleophilic Substitution at the Acyl Carbon / 18:
Synthesis & Reactions of a-Dicarbonyl Compounds: More Chemistry of Enolate Ions / 19:
Amines / 20:
Phenols & Aryl Halides: Nucleophilic Aromatic Substitution / 21:
Carbohydrates / 22:
Lipids / 23:
Amino Acids & Proteins / 24:
Nucleic Acids & Protein Synthesis / 25:
Carbon Compounds and Chemical Bonds / 1:
Representative Carbon Compounds: Functional Groups, Infrared Spectroscopy, & Intermolecular Force / 2:
An Introduction to Organic Reactions: Acids and Bases / 3:
8.

図書

図書
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:
9.

図書

図書
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:
10.

図書

図書
translated [from the German] by F. Sterne; technical editor for English edition K. Littlewood
出版情報: London : Butterworths, 1968  xix, 572 p ; 25 cm
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