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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
by László Kürti and Barbara Czakó ; [foreword by E.J. Corey] ; [introduction by K.C. Nicolaou]
出版情報: Amsterdam ; Tokyo : Elsevier, c2005  lii, 758 p. ; 28 cm
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Foreword / E.J. CoreyI:
Introduction / K.C. NicolaouII:
Preface / III:
Explanation of the Use of Colors in the Schemes and Text / IV:
List of Abbreviations / V:
List of Named Organic Reactions / VI:
Named Organic Reactions in Alphabetical Order / VII:
Appendix: Listing of the Named Reactions by Synthetic Type and by their Utility / VIII:
Brief explanation of the organization of this section / 8.1:
List of named reactions in chronological order of their discovery / 8.2:
Reaction categories - Categorization of named reactions in tabular format / 8.3:
Affected functional groups - Listing of transformations in tabular format / 8.4:
Preparation of functional groups - Listing of transformations in tabular format / 8.5:
References / IX:
Index / X:
Foreword / E.J. CoreyI:
Introduction / K.C. NicolaouII:
Preface / III:
3.

図書

図書
Laura Frost, Todd Deal, Karen C. Timberlake
出版情報: Upper Saddle River, NJ : Prentice Hall, c2011  xvi, 475 p. ; 28 cm
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4.

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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5.

図書

図書
Caroline Cooper
出版情報: Boca Raton, Fla. : CRC Press, Taylor & Francis Group, c2011  xv, 268 p. ; 26 cm
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6.

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:
7.

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:
8.

図書

図書
Michael B. Smith, Jerry March
出版情報: Hoboken, N.J. : John Wiley & Sons, c2007  xx, 2357 p. ; 25 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
9.

図書

図書
edited by Bernd Plietker
出版情報: Weinheim : Wiley-VCH, c2008  xv, 279 p. ; 25 cm
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Preface
List of Contributors
Iron Complexes in Organic Chemistry / Ingmar Bauer ; Hans-Joachim Knolker1:
Introduction / 1.1:
General Aspects of Iron Complex Chemistry / 1.2:
Electronic Configuration, Oxidation States, Structures / 1.2.1:
Fundamental Reactions / 1.2.2:
Organoiron Complexes and Their Applications / 1.3:
Binary Carbonyl-Iron Complexes / 1.3.1:
Alkene-Iron Complexes / 1.3.2:
Allyl- and Trimethylenemethane-Iron Complexes / 1.3.3:
Acyl- and Carbene-Iron Complexes / 1.3.4:
Diene-Iron Complexes / 1.3.5:
Ferrocenes / 1.3.6:
Arene-Iron Complexes / 1.3.7:
Catalysis Using Iron Complexes / 1.4:
Iron Complexes as Substrates and/or Products in Catalytic Reactions / 1.4.1:
Iron Complexes as Ligands for Other Transition Metal Catalysts / 1.4.2:
Iron Complexes as Catalytically Active Species / 1.4.3:
References
Iron Catalysis in Biological and Biomimetic Reactions / 2:
Non-heme Iron Catalysts in Biological and Biomimetic Transformations / Jens Muller2.1:
Introduction: Iron in Biological Processes / 2.1.1:
Non-heme Iron Proteins / 2.1.2:
Mononuclear Iron Sites / 2.1.2.1:
Dinuclear Iron Sites / 2.1.2.2:
Summary / 2.1.3:
Organic Reactions Catalyzed by Heme Proteins / Martin Broring2.2:
Classification and General Reactivity Schemes of Heme Proteins Used in Organic Synthesis / 2.2.1:
Organic Reactions Catalyzed by Cytochromes P450 / 2.2.2:
Organic Reactions Catalyzed by Heme Peroxidases / 2.2.3:
Dehydrogenations ("Peroxidase Reactivity") / 2.2.3.1:
Sulfoxidations ("Peroxygenase Reactivity") / 2.2.3.2:
Peroxide Disproportionation ("Catalase Reactivity") / 2.2.3.3:
Halogenation ("Haloperoxidase Reactivity") / 2.2.3.4:
Epoxidations ("Monoxygenase Activity") / 2.2.3.5:
Iron-catalyzed Oxidation Reactions / 3:
Oxidations of C-H and C=C Bonds / Agathe Christine Mayer ; Carsten Bolm3.1:
Gif Chemistry / 3.1.1:
Alkene Epoxidation / 3.1.2:
Alkene Dihydroxylation / 3.1.3:
The Kharasch Reaction and Related Reactions / 3.1.4:
Aziridination and Diamination / 3.1.5:
Oxidative Allylic Oxygenation and Amination / Sabine Laschat ; Volker Rabe ; Angelika Baro3.2:
Iron-catalyzed Allylic Oxidations / 3.2.1:
Simple Iron Salts / 3.2.2.1:
Fe(III) Complexes with Bidentate Ligands / 3.2.2.2:
Fe[superscript 3+]/Fe[superscript 2+] Porphyrin and Phthalocyanine Complexes / 3.2.2.3:
Iron(III) Salen Complexes / 3.2.2.4:
Non-heme Iron Complexes with Tetra- and Pentadentate Ligands / 3.2.2.5:
Oxidative Allylic Aminations / 3.2.3:
Conclusion / 3.2.4:
Oxidation of Heteroatoms (N and S) / Olga Garcia Mancheno3.3:
Oxidation of Nitrogen Compounds / 3.3.1:
Oxidation of Hydroxylamines to Nitroso Compounds / 3.3.1.1:
Oxidation of Arylamines / 3.3.1.2:
Other N-Oxidations / 3.3.1.3:
Oxidation of Sulfur Compounds / 3.3.2:
Oxidation of Thiols to Disulfides / 3.3.2.1:
Oxidation of Sulfides / 3.3.2.2:
Oxidative Imination of Sulfur Compounds / 3.3.2.3:
Reduction of Unsaturated Compounds with Homogeneous Iron Catalysts / Stephan Enthaler ; Kathrin Junge ; Matthias Beller4:
Hydrogenation of Carbonyl Compounds / 4.1:
Hydrogenation of Carbon-Carbon Double Bonds / 4.3:
Hydrogenation of Imines and Similar Compounds / 4.4:
Catalytic Hydrosilylations / 4.5:
Iron-catalyzed Cross-coupling Reactions / Andreas Leitner4.6:
Cross-coupling Reactions of Alkenyl Electrophiles / 5.1:
Cross-coupling Reactions of Aryl Electrophiles / 5.3:
Cross-coupling Reactions of Alkyl Electrophiles / 5.4:
Cross-coupling Reactions of Acyl Electrophiles / 5.5:
Iron-catalyzed Carbometallation Reactions / 5.6:
Iron-catalyzed Aromatic Substitutions / Jette Kischel ; Kristin Mertins ; Irina Jovel ; Alexander Zapf5.7:
General Aspects / 6.1:
Electrophilic Aromatic Substitutions / 6.2:
Halogenation Reactions / 6.2.1:
Nitration Reactions / 6.2.2:
Sulfonylation Reactions / 6.2.3:
Friedel-Crafts Acylations / 6.2.4:
Friedel-Crafts Alkylations / 6.2.5:
Alkylation with Alcohols, Ethers and Esters / 6.2.5.1:
Alkylation with Alkenes / 6.2.5.2:
Nucleophilic Aromatic Substitutions / 6.3:
Iron-catalyzed Substitution Reactions / Bernd Plietker7:
Iron-catalyzed Nucleophilic Substitutions / 7.1:
Nucleophilic Substitutions of Non-activated C-X Bonds / 7.2.1:
Nucleophilic Substitutions Using Lewis Acidic Fe Catalysts / 7.2.1.1:
Substitutions Catalyzed by Ferrate Complexes / 7.2.1.3:
Nucleophilic Substitution of Allylic and Propargylic C-X Bonds / 7.2.2:
Reactions Catalyzed by Lewis Acidic Fe Salts / 7.2.2.1:
Nucleophilic Substitutions Involving Ferrates / 7.2.2.2:
Addition and Conjugate Addition Reactions to Carbonyl Compounds / Jens Christoffers ; Herbert Frey ; Anna Rosiak7.3:
Additions to Aldehydes and Ketones / 8.1:
Oxygen Nucleophiles / 8.2.1:
Carbon Nucleophiles / 8.2.2:
Additions to Imines and Iminium Ions / 8.3:
Additions to Carboxylic Acids and Their Derivatives / 8.4:
Conjugate Addition to [alpha],[beta]-Unsaturated Carbonyl Compounds / 8.4.1:
Michael Reactions / 8.5.1:
Vinylogous Michael Reactions / 8.5.1.2:
Asymmetric Michael Reactions / 8.5.1.3:
Michael Reactions in Ionic Liquids and Heterogeneous Catalysis / 8.5.1.4:
Nitrogen Nucleophiles / 8.5.2:
Synthesis of Heterocycles / 8.6:
Pyridine and Quinoline Derivatives / 8.6.1:
Pyrimidine and Pyrazine Derivatives / 8.6.2:
Benzo- and Dibenzopyrans / 8.6.3:
Iron-catalyzed Cycloadditions and Ring Expansion Reactions / Gerhard Hilt ; Judith Janikowski9:
Cycloisomerization and Alder-Ene Reaction / 9.1:
[2+1]-Cycloadditions / 9.3:
Iron-catalyzed Aziridine Formation / 9.3.1:
Iron-catalyzed Epoxide Formation / 9.3.2:
Iron-catalyzed Cyclopropane Formation / 9.3.3:
[2+2]-Cycloaddition / 9.4:
[4+1]-Cycloadditions / 9.5:
[4+2]-Cycloadditions / 9.6:
Diels-Alder Reactions with Normal Electron Demand / 9.6.1:
Diels-Alder Reactions with Neutral Electron Demand / 9.6.2:
Diels-Alder Reactions with Inverse Electron Demand / 9.6.3:
Cyclotrimerization / 9.7:
[3+2]-Cycloadditions / 9.8:
[3+3]-Cycloadditions / 9.9:
Ring Expansion Reactions / 9.10:
Index / 9.11:
Preface
List of Contributors
Iron Complexes in Organic Chemistry / Ingmar Bauer ; Hans-Joachim Knolker1:
10.

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
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