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Name Reactions

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Table of Contents

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    Book Overview
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    Chapter 1 Abnormal Claisen rearrangement
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    Chapter 2 Alder ene reaction
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    Chapter 3 Aldol condensation
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    Chapter 4 Allan-Robinson reaction
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    Chapter 5 Alper carbonylation
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    Chapter 6 Amadori rearrangement
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    Chapter 8 ANRORC mechanism
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    Chapter 9 Arndt-Eistert homologation
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    Chapter 10 Auwers reaction
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    Chapter 11 Baeyer-Drewson indigo synthesis
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    Chapter 12 Baeyer-Villiger oxidation
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    Chapter 13 Baker-Venkataraman rearrangement
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    Chapter 14 Bamberger rearrangement
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    Chapter 15 Bamford-Stevens reaction
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    Chapter 16 Bargellini reaction
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    Chapter 17 Bartoli indole synthesis
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    Chapter 18 Barton decarboxylation
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    Chapter 19 Barton-McCombie deoxygenation
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    Chapter 20 Barton nitrite photolysis
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    Chapter 24 Benzilic acid rearrangement
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    Chapter 25 Benzoin condensation
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    Chapter 26 Bergman cyclization
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    Chapter 28 Birch reduction
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    Chapter 29 Bischler-Möhlau indole synthesis
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    Chapter 31 Blaise reaction
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    Chapter 32 Blanc chloromethylation reaction
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    Chapter 33 Boekelheide reaction
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    Chapter 34 Boger pyridine synthesis
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    Chapter 35 Boord reaction
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    Chapter 36 Borsche-Drechsel cyclization
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    Chapter 37 Boulton-Katritzky rearrangement
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    Chapter 41 Bradsher reaction
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    Chapter 43 Brown hydroboration reaction
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    Chapter 44 Bucherer carbazole synthesis
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    Chapter 45 Bucherer reaction
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    Chapter 46 Bucherer-Bergs reaction
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    Chapter 48 Buchner method of ring expansion
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    Chapter 49 Buchwald-Hartwig C-N bond and C-O bond formation reactions
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    Chapter 53 Carroll rearrangement
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    Chapter 54 Castro-Stephens coupling
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    Chapter 55 Chapman rearrangement
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    Chapter 56 Chichibabin amination reaction
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    Chapter 58 Chugaev elimination
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    Chapter 60 Claisen condensation
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    Chapter 63 Clemmensen reduction
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    Chapter 64 Combes quinoline synthesis
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    Chapter 65 Conrad-Limpach reaction
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    Chapter 66 Cook-Heilbron thiazole synthesis
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    Chapter 68 Cope, oxy-Cope, and anionic oxy-Cope rearrangements
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    Chapter 69 Corey-Bakshi-Shibata (CBS) reduction
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    Chapter 71 Corey-Fuchs reaction
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    Chapter 73 Corey-Winter olefin synthesis
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    Chapter 74 Cornforth rearrangement
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    Chapter 75 Criegee glycol cleavage
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    Chapter 76 Criegee mechanism of ozonolysis
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    Chapter 78 Dakin oxidation
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    Chapter 79 Dakin-West reaction
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    Chapter 80 Danheiser annulation
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    Chapter 81 Darzens glycidic ester condensation
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    Chapter 82 Davis chiral oxaziridine reagents
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    Chapter 84 Demjanov rearrangement
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    Chapter 86 Dieckmann condensation
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    Chapter 87 Diels-Alder reaction
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    Chapter 89 Di- π -methane rearrangement
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    Chapter 90 Doebner reaction
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    Chapter 91 Doebner–von Miller reaction
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    Chapter 92 Doering–LaFlamme allene synthesis
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    Chapter 93 Dornow–Wiehler isoxazole synthesis
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    Chapter 94 Dötz reaction
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    Chapter 95 Dowd ring expansion
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    Chapter 96 Dutt-wormall reaction
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    Chapter 97 Eglinton reaction
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    Chapter 99 Eschenmoser-Tanabe fragmentation
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    Chapter 100 Étard reaction
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    Chapter 101 Evans aldol reaction
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    Chapter 102 Favorskii rearrangement and Quasi-Favorskii rearrangement
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    Chapter 103 Feist-Bénary furan synthesis
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    Chapter 104 Ferrier rearrangement
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    Chapter 105 Finkelstein reaction
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    Chapter 106 Fischer-Hepp rearrangement
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    Chapter 108 Fischer-Speier esterification
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    Chapter 110 Forster reaction
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    Chapter 111 Frater-Seebach alkylation
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    Chapter 112 Friedel-Crafts reaction
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    Chapter 113 Friedländer synthesis
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    Chapter 114 Fries rearrangement
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    Chapter 115 Fritsch-Buttenberg-Wiechell rearrangement
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    Chapter 117 Fukuyama amine synthesis
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    Chapter 119 Gassman indole synthesis
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    Chapter 121 Gewald aminothiophene synthesis
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    Chapter 123 Gomberg-Bachmann reaction
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    Chapter 125 Gribble reduction of diaryl ketones
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    Chapter 126 Grignard reaction
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    Chapter 127 Grob fragmentation
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    Chapter 128 Guareschi-Thorpe condensation
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    Chapter 129 Hajos-Wiechert reaction
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    Chapter 130 Haller-Bauer reaction
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    Chapter 131 Hantzsch pyridine synthesis
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    Chapter 132 Hantzsch pyrrole synthesis
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    Chapter 133 Haworth reaction
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    Chapter 134 Hayashi rearrangement
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    Chapter 135 Heck reaction
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    Chapter 136 Hegedus indole synthesis
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    Chapter 137 Hell-Volhardt-Zelinsky reaction
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    Chapter 138 Henry reaction (nitroaldol reaction)
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    Chapter 139 Herz reaction
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    Chapter 140 Heteroaryl Heck reaction
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    Chapter 142 Doering–LaFlamme allene synthesis
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    Chapter 143 Hodges-Vedejs metallation of oxazoles
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    Chapter 144 Hofmann rearrangement (Hofmann degradation reaction)
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    Chapter 146 Hofmann-Martius reaction
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    Chapter 148 Horner-Wadsworth-Emmons reaction
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    Chapter 149 Houben-Hoesch reaction
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    Chapter 151 Ing-Manske procedure
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    Chapter 152 Jacobsen-Katsuki epoxidation
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    Chapter 153 Jacobsen rearrangement
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    Chapter 155 Julia-Lythgoe olefination
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    Chapter 157 Keck stereoselective allylation
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    Chapter 158 Keck macrolactonization
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    Chapter 159 Kemp elimination
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    Chapter 160 Kennedy oxidative cyclization
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    Chapter 161 Kharasch addition reaction
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    Chapter 162 Knöevenagel condensation
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    Chapter 163 Knorr pyrrole synthesis
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    Chapter 164 Koch carbonylation reaction (Koch-Haaf carbonylation reaction)
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    Chapter 165 Koenig-Knorr glycosidation
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    Chapter 166 Kolbe electrolytic coupling
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    Chapter 167 Kolbe-Schmitt reaction
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    Chapter 168 Kostanecki reaction
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    Chapter 170 Kröhnke reaction (pyridine synthesis)
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    Chapter 171 Kumada cross-coupling reaction
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    Chapter 172 Larock indole synthesis
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    Chapter 173 Lawesson’s reagent
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    Chapter 174 Leuckart-Wallach reaction
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    Chapter 175 Lieben haloform reaction
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    Chapter 176 Liebeskind-Srogl coupling
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    Chapter 178 Luche reduction
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    Chapter 179 McFadyen-Stevens reduction
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    Chapter 180 McLafferty fragmentation
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    Chapter 181 McMurry coupling
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    Chapter 182 Madelung indole synthesis
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    Chapter 183 Mannich reaction
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    Chapter 185 Martin’s sulfurane dehydrating reagent
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    Chapter 187 Meerwein arylation
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    Chapter 188 Meerwein-Ponndorf-Verley reduction
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    Chapter 189 Meinwald rearrangement
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    Chapter 191 Meisenheimer rearrangement
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    Chapter 193 Michael addition
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    Chapter 194 Michaelis-Arbuzov phosphonate synthesis
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    Chapter 195 Midland reduction
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    Chapter 196 Miller-Loudon-Snyder nitrile synthesis
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    Chapter 197 Mislow-Evans rearrangement
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    Chapter 198 Mitsunobu reaction
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    Chapter 199 Miyaura boration reaction
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    Chapter 200 Moffatt oxidation
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    Chapter 201 Morgan-Walls reaction (Pictet-Hubert reaction)
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    Chapter 202 Mori-Ban indole synthesis
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    Chapter 203 Morin rearrangement
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    Chapter 204 Mukaiyama aldol reaction
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    Chapter 205 Mukaiyama esterification
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    Chapter 207 Nametkin rearrangement (Retropinacol rearrangement)
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    Chapter 209 Neber rearrangement
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    Chapter 210 Nef reaction
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    Chapter 211 Negishi cross-coupling reaction
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    Chapter 212 Nenitzescu indole synthesis
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    Chapter 213 Nicholas reaction
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    Chapter 215 Nozaki-Hiyama-Kishi reaction
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    Chapter 217 Orton rearrangement
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    Chapter 219 Paal-Knorr furan synthesis
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    Chapter 220 Paal-Knorr pyrrole synthesis
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    Chapter 222 Passerini reaction
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    Chapter 224 Pauson-Khand cyclopentenone synthesis
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    Chapter 225 Payne rearrangement
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    Chapter 226 Pechmann condensation (coumarin synthesis)
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    Chapter 228 Perkin reaction (cinnamic acid synthesis)
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    Chapter 230 Peterson olefination
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    Chapter 231 Pfau-Plattner azulene synthesis
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    Chapter 232 Pfitzinger quinoline synthesis
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    Chapter 233 Pictet-Gams isoquinoline synthesis
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    Chapter 234 Pictet-Spengler tetrahydroisoquinoline synthesis
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    Chapter 235 Pinacol rearrangement
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    Chapter 236 Pinner synthesis
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    Chapter 237 Polonovski reaction
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    Chapter 238 Polonovski-Potier reaction
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    Chapter 239 Pomeranz-Fritsch reaction
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    Chapter 241 Prilezhaev reaction
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    Chapter 242 Prins reaction
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    Chapter 243 Pschorr ring closure
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    Chapter 245 Ramberg—Bäcklund olefin synthesis
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    Chapter 246 Reformatsky reaction
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    Chapter 247 Regitz diazo synthesis
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    Chapter 249 Reissert reaction (aldehyde synthesis)
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    Chapter 250 Riley oxidation (selenium dioxide oxidation)
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    Chapter 251 Ring-closing metathesis (RCM) using Grubbs and Schrock catalysts
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    Chapter 253 Robinson annulation
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    Chapter 254 Robinson-Schöpf reaction
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    Chapter 255 Rosenmund reduction
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    Chapter 256 Roush allylboronate reagent
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    Chapter 257 Rubottom oxidation
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    Chapter 259 Rychnovsky polyol synthesis
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    Chapter 260 Sakurai allylation reaction (Hosomi-Sakurai reaction)
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    Chapter 262 Sarett oxidation
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    Chapter 263 Schiemann reaction (Balz-Schiemann reaction)
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    Chapter 264 Schlosser modification of the Wittig reaction
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    Chapter 265 Schmidt reaction
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    Chapter 266 Schmidt’s trichloroacetimidate glycosidation reaction
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    Chapter 267 Scholl reaction
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    Chapter 268 Schöpf reaction
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    Chapter 269 Schotten-Baumann reaction
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    Chapter 270 Shapiro reaction
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    Chapter 271 Sharpless asymmetric amino hydroxylation
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    Chapter 272 Sharpless asymmetric epoxidation
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    Chapter 273 Sharpless dihydroxylation
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    Chapter 274 Shi asymmetric epoxidation
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    Chapter 275 Simmons-Smith reaction
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    Chapter 277 Simonis chromone cyclization
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    Chapter 279 Smiles rearrangement
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    Chapter 281 Sommelet-Hauser (ammonium ylide) rearrangement
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    Chapter 282 Sonogashira reaction
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    Chapter 283 Staudinger reaction
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    Chapter 284 Stetter reaction (Michael-Stetter reaction)
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    Chapter 285 Stevens rearrangement
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    Chapter 286 Stieglitz rearrangement
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    Chapter 287 Still-gennari phosphonate reaction
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    Chapter 288 Stille coupling
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    Chapter 289 Stille-kelly reaction
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    Chapter 290 Stobbe condensation
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    Chapter 292 Stork enamine reaction
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    Chapter 294 Suzuki coupling
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    Chapter 295 Swern oxidation
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    Chapter 296 Tamao-Kumada oxidation
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    Chapter 297 Tebbe olefination (Petasis alkenylation)
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    Chapter 298 Thorpe-Ziegler reaction
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    Chapter 299 Tiemann rearrangement
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    Chapter 300 Tiffeneau-Demjanov Rearrangement
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    Chapter 301 Tishchenko reaction
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    Chapter 302 Tollens reaction
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    Chapter 303 Tsuji-Trost reaction
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    Chapter 304 Ueno-Stork cyclization
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    Chapter 305 Ugi reaction
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    Chapter 307 Vilsmeier—Haack reaction
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    Chapter 309 Von Richter reaction
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    Chapter 310 Wacker oxidation
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    Chapter 311 Wagner-Meerwein rearrangement
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    Chapter 314 Weiss reaction
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    Chapter 316 Wharton oxygen transposition reaction
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    Chapter 318 Williamson ether synthesis
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    Chapter 320 [1,2]-Wittig rearrangement
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    Chapter 321 [2,3]-Wittig rearrangement
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    Chapter 322 Wohl-Ziegler reaction
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    Chapter 324 Wolff-Kishner reduction
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    Chapter 326 Wurtz reaction
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    Chapter 327 Yamada coupling reagent
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    Chapter 328 Yamaguchi esterification
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    Chapter 329 Zaitsev elimination
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    Chapter 331 Zinin benzidine rearrangement (semidine rearrangement)
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Title
Name Reactions
Published by
Springer-Verlag Berlin Heidelberg, January 2003
DOI 10.1007/978-3-662-05336-2
ISBNs
978-3-66-205336-2, 978-3-66-205338-6
Authors

Jie Jack Li, Li, Jie Jack

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The data shown below were compiled from readership statistics for 39 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Belgium 1 3%
Unknown 38 97%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 7 18%
Student > Master 6 15%
Student > Bachelor 4 10%
Researcher 4 10%
Student > Doctoral Student 3 8%
Other 2 5%
Unknown 13 33%
Readers by discipline Count As %
Chemistry 21 54%
Biochemistry, Genetics and Molecular Biology 1 3%
Pharmacology, Toxicology and Pharmaceutical Science 1 3%
Medicine and Dentistry 1 3%
Materials Science 1 3%
Other 0 0%
Unknown 14 36%