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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 Alder ene reaction
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    Chapter 2 Aldol condensation
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    Chapter 3 Algar-Flynn-Oyamada Reaction
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    Chapter 5 Appel reaction
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    Chapter 6 Arndt-Eistert homologation
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    Chapter 7 Baeyer-Villiger oxidation
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    Chapter 8 Baker-Venkataraman rearrangement
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    Chapter 9 Bamberger rearrangement
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    Chapter 10 Bamford-Stevens reaction
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    Chapter 11 Barbier coupling reaction
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    Chapter 12 Bargellini reaction
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    Chapter 13 Bartoli indole synthesis
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    Chapter 14 Barton radical decarboxylation
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    Chapter 15 Barton-McCombie deoxygenation
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    Chapter 16 Barton nitrite photolysis
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    Chapter 17 Barton-Zard reaction
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    Chapter 18 Batcho-Leimgruber indole synthesis
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    Chapter 19 Baylis-Hillman reaction
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    Chapter 20 Beckmann rearrangement
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    Chapter 21 Beirut reaction
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    Chapter 22 Benzilic acid rearrangement
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    Chapter 23 Benzoin condensation
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    Chapter 24 Bergman cyclization
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    Chapter 25 Biginelli pyrimidone synthesis
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    Chapter 28 Bischler-Napieralski reaction
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    Chapter 29 Blaise reaction
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    Chapter 30 Blanc chloromethylation
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    Chapter 31 Blum aziridine synthesis
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    Chapter 32 Boekelheide reaction
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    Chapter 33 Boger pyridine synthesis
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    Chapter 34 Borch reductive amination
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    Chapter 35 Borsche-Drechsel cyclization
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    Chapter 36 Boulton-Katritzky rearrangement
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    Chapter 37 Bouveault aldehyde synthesis
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    Chapter 38 Bouveault-Blanc reduction
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    Chapter 39 Boyland-Sims oxidation
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    Chapter 40 Bradsher reaction
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    Chapter 41 Brook rearrangement
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    Chapter 42 Brown hydroboration
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    Chapter 43 Bucherer carbazole synthesis
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    Chapter 45 Bucherer-Bergs reaction
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    Chapter 46 Büchner-Curtius-Schlotterbeck reaction
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    Chapter 47 Büchner method of ring expansion
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    Chapter 48 Buchwald-Hartwig C-N and C-O bond formation reactions
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    Chapter 49 Burgess dehydrating reagent
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    Chapter 50 Cadiot-Chodkiewicz coupling
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    Chapter 51 Camps quinolinol synthesis
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    Chapter 52 Cannizzaro disproportionation
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    Chapter 53 Carroll rearrangement
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    Chapter 54 Castro-Stephens coupling
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    Chapter 55 Chan alkyne reduction
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    Chapter 57 Chapman rearrangement
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    Chapter 58 Chichibabin pyridine synthesis
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    Chapter 59 Chugaev elimination
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    Chapter 60 Ciamician-Dennsted rearrangement
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    Chapter 61 Claisen condensation
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    Chapter 62 Claisen isoxazole synthesis
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    Chapter 63 Claisen rearrangements
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    Chapter 64 Clemmensen reduction
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    Chapter 65 Combes quinoline synthesis
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    Chapter 66 Conrad-Limpach reaction
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    Chapter 67 Cope elimination reaction
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    Chapter 68 Cope rearrangement
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    Chapter 70 Corey-Chaykovsky reaction
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    Chapter 71 Corey-Fuchs reaction
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    Chapter 72 Corey-Kim oxidation
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    Chapter 73 Corey-Nicolaou macrolactonization
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    Chapter 74 Corey-Seebach reaction
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    Chapter 75 Corey-Winter olefin synthesis
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    Chapter 76 Criegee glycol cleavage
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    Chapter 77 Criegee mechanism of ozonolysis
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    Chapter 79 Dakin oxidation
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    Chapter 80 Dakin-West reaction
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    Chapter 81 Danheiser annulation
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    Chapter 82 Darzens glycidic ester condensation
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    Chapter 83 Davis chiral oxaziridine reagents
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    Chapter 84 Delépine amine synthesis
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    Chapter 85 de Mayo reaction
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    Chapter 87 Dess-Martin periodinane oxidation
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    Chapter 88 Dieckmann condensation
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    Chapter 89 Diels-Alder reaction
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    Chapter 90 Dienone-phenol rearrangement
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    Chapter 92 Doebner quinoline synthesis
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    Chapter 93 Dötz reaction
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    Chapter 94 Dowd-Beckwith ring expansion
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    Chapter 95 Erlenmeyer-Plöchl azlactone synthesis
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    Chapter 97 Eschweiler-Clarke reductive alkylation of amines
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    Chapter 98 Evans aldol reaction
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    Chapter 99 Favorskii rearrangement and quasi-Favorskii rearrangement
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    Chapter 100 Feist-Bénary furan synthesis
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    Chapter 101 Ferrier carbocyclization
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    Chapter 102 Ferrier glycal allylic rearrangement
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    Chapter 103 Fiesselmann thiophene synthesis
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    Chapter 106 Fleming-Kumada oxidation
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    Chapter 109 Fries rearrangement
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    Chapter 110 Fukuyama amine synthesis
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    Chapter 111 Fukuyama reduction
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    Chapter 112 Gabriel synthesis
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    Chapter 113 Gabriel-Colman rearrangement
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    Chapter 114 Gassman indole synthesis
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    Chapter 115 Gattermann-Koch reaction
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    Chapter 116 Gewald aminothiophene synthesis
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    Chapter 117 Glaser coupling
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    Chapter 118 Gomberg-Bachmann reaction
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    Chapter 119 Gould-Jacobs reaction
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    Chapter 120 Grignard reaction
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    Chapter 121 Grob fragmentation
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    Chapter 123 Hajos-Wiechert reaction
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    Chapter 124 Haller-Bauer reaction
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    Chapter 125 Hantzsch dihydropyridine synthesis
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    Chapter 126 Hantzsch pyrrole synthesis
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    Chapter 127 Heck reaction
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    Chapter 128 Hegedus indole synthesis
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    Chapter 129 Hell-Volhard-Zelinsky reaction
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    Chapter 130 Henry nitroaldol reaction
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    Chapter 131 Hinsberg synthesis of thiophene derivatives
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    Chapter 133 Hofmann rearrangement
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    Chapter 135 Horner-Wadsworth-Emmons reaction
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    Chapter 136 Houben-Hoesch reaction
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    Chapter 137 Hunsdiecker-Borodin reaction
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    Chapter 138 Hurd-Mori 1,2,3-thiadiazole synthesis
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    Chapter 140 Japp-Klingemann hydrazone synthesis
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    Chapter 141 Jones oxidation
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    Chapter 142 Julia-Kocienski olefination
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    Chapter 143 Julia-Lythgoe olefination
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    Chapter 144 Kahne-Crich glycosidation
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    Chapter 145 Keck macrolactonization
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    Chapter 146 Knoevenagel condensation
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    Chapter 147 Knorr pyrazole synthesis
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    Chapter 148 Koch-Haaf carbonylation
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    Chapter 149 Koenig-Knorr glycosidation
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    Chapter 150 Kolbe-Schmitt reaction
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    Chapter 151 Kostanecki reaction
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    Chapter 152 Kröhnke pyridine synthesis
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    Chapter 153 Kumada cross-coupling reaction
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    Chapter 154 Lawesson’s reagent
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    Chapter 155 Leuckart-Wallach reaction
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    Chapter 156 Lossen rearrangement
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    Chapter 157 McFadyen-Stevens reduction
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    Chapter 158 McMurry coupling
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    Chapter 159 MacMillan catalyst
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    Chapter 160 Mannich reaction
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    Chapter 161 Marshall boronate fragmentation
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    Chapter 162 Martin’s sulfurane dehydrating reagent
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    Chapter 163 Masamune-Roush conditions
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    Chapter 164 Meerwein-Ponndorf-Verley reduction
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    Chapter 166 [1,2]-Meisenheimer rearrangement
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    Chapter 167 [2,3]-Meisenheimer rearrangement
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    Chapter 168 Meth-Cohn quinoline synthesis
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    Chapter 169 Meyers oxazoline method
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    Chapter 170 Meyer-Schuster rearrangement
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    Chapter 171 Michael addition
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    Chapter 172 Michaelis-Arbuzov phosphonate synthesis
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    Chapter 173 Midland reduction
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    Chapter 174 Mislow-Evans rearrangement
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    Chapter 175 Mitsunobu reaction
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    Chapter 176 Miyaura borylation
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    Chapter 177 Moffatt oxidation
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    Chapter 178 Montgomery coupling
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    Chapter 179 Morgan-Walls reaction
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    Chapter 180 Mori-Ban indole synthesis
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    Chapter 181 Mukaiyama aldol reaction
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    Chapter 182 Mukaiyama Michael addition
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    Chapter 183 Mukaiyama reagent
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    Chapter 184 Myers-Saito cyclization
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    Chapter 185 Nazarov cyclization
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    Chapter 186 Neber rearrangement
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    Chapter 187 Nef reaction
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    Chapter 188 Negishi cross-coupling reaction
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    Chapter 189 Nenitzescu indole synthesis
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    Chapter 190 Nicholas reaction
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    Chapter 191 Nicolaou dehydrogenation
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    Chapter 192 Nicolaou hydroxy-dithioketal cyclization
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    Chapter 194 Nicolaou oxyselenation
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    Chapter 195 Noyori asymmetric hydrogenation
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    Chapter 196 Nozaki-Hiyama-Kishi reaction
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    Chapter 197 Oppenauer oxidation
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    Chapter 199 Paal thiophene synthesis
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    Chapter 200 Paal-Knorr furan synthesis
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    Chapter 201 Parham cyclization
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    Chapter 202 Passerini reaction
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    Chapter 203 Paternó-Büchi reaction
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    Chapter 205 Payne rearrangement
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    Chapter 206 Pechmann coumarin synthesis
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    Chapter 207 Perkin reaction
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    Chapter 208 Petasis reaction
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    Chapter 210 Pictet-Gams isoquinoline synthesis
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    Chapter 211 Pictet-Spengler tetrahydroisoquinoline synthesis
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    Chapter 212 Pinacol rearrangement
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    Chapter 213 Pinner reaction
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    Chapter 214 Polonovski reaction
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    Chapter 215 Polonovski-Potier reaction
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    Chapter 216 Pomeranz-Fritsch reaction
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    Chapter 217 Prévost trans -dihydroxylation
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    Chapter 219 Pschorr cyclization
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    Chapter 220 Pummerer rearrangement
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    Chapter 221 Ramberg-Bäcklund reaction
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    Chapter 223 Regitz diazo synthesis
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    Chapter 224 Reimer-Tiemann reaction
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    Chapter 225 Reissert aldehyde synthesis
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    Chapter 226 Reissert indole synthesis
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    Chapter 227 Ring-closing metathesis (RCM)
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    Chapter 228 Ritter reaction
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    Chapter 230 Robinson-Gabriel synthesis
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    Chapter 231 Robinson-Schöpf reaction
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    Chapter 232 Rosenmund reduction
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    Chapter 233 Rubottom oxidation
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    Chapter 234 Rupe rearrangement
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    Chapter 235 Saegusa oxidation
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    Chapter 236 Sakurai allylation reaction
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    Chapter 237 Sandmeyer reaction
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    Chapter 238 Schiemann reaction
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    Chapter 239 Schmidt reaction
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    Chapter 240 Schmidt’s trichloroacetimidate glycosidation reaction
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    Chapter 241 Shapiro reaction
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    Chapter 242 Sharpless asymmetric amino hydroxylation
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    Chapter 243 Sharpless asymmetric epoxidation
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    Chapter 246 Simmons-Smith reaction
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    Chapter 247 Skraup quinoline synthesis
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    Chapter 249 Sommelet reaction
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    Chapter 250 Sommelet-Hauser rearrangement
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    Chapter 251 Sonogashira reaction
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    Chapter 252 Staudinger ketene cycloaddition
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    Chapter 254 Sternbach benzodiazepine synthesis
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    Chapter 255 Stetter reaction
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    Chapter 256 Still-Gennari phosphonate reaction
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    Chapter 257 Stille coupling
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    Chapter 258 Stille-Kelly reaction
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    Chapter 259 Stobbe condensation
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    Chapter 260 Stork enamine reaction
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    Chapter 261 Strecker amino acid synthesis
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    Chapter 262 Suzuki coupling
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    Chapter 263 Swern oxidation
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    Chapter 264 Takai iodoalkene synthesis
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    Chapter 265 Tebbe olefination
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    Chapter 266 TEMPO-mediated oxidation
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    Chapter 267 Thorpe-Ziegler reaction
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    Chapter 268 Tsuji-Trost reaction
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    Chapter 269 Ugi reaction
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    Chapter 270 Ullmann reaction
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    Chapter 272 Vilsmeier-Haack reaction
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    Chapter 273 Vilsmeier mechanism for acid chloride formation
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    Chapter 274 Vinylcyclopropane-cyclopentene rearrangement
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    Chapter 275 von Braun reaction
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    Chapter 276 Wacker oxidation
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    Chapter 277 Wagner-Meerwein rearrangement
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    Chapter 278 Weiss-Cook reaction
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    Chapter 279 Wharton oxygen transposition reaction
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    Chapter 280 Willgerodt-Kindler reaction
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    Chapter 282 [1,2]-Wittig rearrangement
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    Chapter 283 [2,3]-Wittig rearrangement
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    Chapter 284 Wohl-Ziegler reaction
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    Chapter 285 Wolff rearrangement
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    Chapter 286 Wolff-Kishner reduction
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    Chapter 287 Yamaguchi esterification
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    Chapter 288 Zincke reaction
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Title
Name Reactions
Published by
Springer Berlin Heidelberg, January 2006
DOI 10.1007/3-540-30031-7
ISBNs
978-3-54-030030-4, 978-3-54-030031-1
Authors

Li, Jie Jack

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Geographical breakdown

Country Count As %
Portugal 1 <1%
Germany 1 <1%
Switzerland 1 <1%
South Africa 1 <1%
Poland 1 <1%
Unknown 139 97%

Demographic breakdown

Readers by professional status Count As %
Student > Ph. D. Student 31 22%
Student > Bachelor 29 20%
Student > Master 20 14%
Researcher 13 9%
Student > Doctoral Student 7 5%
Other 22 15%
Unknown 22 15%
Readers by discipline Count As %
Chemistry 91 63%
Chemical Engineering 9 6%
Agricultural and Biological Sciences 5 3%
Biochemistry, Genetics and Molecular Biology 4 3%
Medicine and Dentistry 3 2%
Other 9 6%
Unknown 23 16%