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Name Reactions : A Collection of Detailed Mechanisms and Synthetic Applications Fifth Edition

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Cover of 'Name Reactions : A Collection of Detailed Mechanisms and Synthetic Applications Fifth Edition'

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 4 Allan–Robinson reaction
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    Chapter 7 Baker–Venkataraman rearrangement
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    Chapter 8 Bamford–Stevens reaction
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    Chapter 9 Baran reagents
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    Chapter 10 Barbier reaction
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    Chapter 11 Bargellini reaction
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    Chapter 12 Bartoli indole synthesis
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    Chapter 13 Barton radical decarboxylation
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    Chapter 14 Barton–McCombie deoxygenation
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    Chapter 15 Barton nitrite photolysis
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    Chapter 16 Barton–Zard reaction
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    Chapter 17 Batcho–Leimgruber indole synthesis
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    Chapter 18 Baylis–Hillman reaction
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    Chapter 19 Beckmann rearrangement
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    Chapter 20 Beirut reaction
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    Chapter 21 Benzilic acid rearrangement
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    Chapter 22 Benzoin condensation
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    Chapter 23 Bergman cyclization
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    Chapter 26 Bischler–Möhlau indole synthesis
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    Chapter 27 Bischler–Napieralski reaction
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    Chapter 28 Blaise reaction
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    Chapter 29 Blum–Ittah aziridine synthesis
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    Chapter 30 Boekelheide reaction
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    Chapter 31 Boger pyridine synthesis
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    Chapter 32 Borch reductive amination
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    Chapter 33 Borsche–Drechsel cyclization
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    Chapter 35 Bouveault aldehyde synthesis
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    Chapter 36 Bouveault–Blanc reduction
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    Chapter 37 Boyland–Sims oxidation
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    Chapter 38 Bradsher reaction
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    Chapter 39 Brook rearrangement
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    Chapter 40 Brown hydroboration
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    Chapter 41 Bucherer carbazole synthesis
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    Chapter 42 Bucherer reaction
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    Chapter 43 Bucherer–Bergs reaction
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    Chapter 44 Büchner ring expansion
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    Chapter 45 Buchwald–Hartwig amination
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    Chapter 46 Burgess reagent
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    Chapter 47 Burke boronates
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    Chapter 48 Cadiot–Chodkiewicz coupling
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    Chapter 50 Camps quinoline synthesis
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    Chapter 51 Cannizzaro reaction
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    Chapter 52 Carroll rearrangement
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    Chapter 53 Castro–Stephens coupling
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    Chapter 54 C–H activation
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    Chapter 55 Chan alkyne reduction
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    Chapter 56 Chan–Lam C–X coupling reaction
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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 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 78 Curtius rearrangement
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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 83 Delépine amine synthesis
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    Chapter 84 de Mayo reaction
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    Chapter 85 Demjanov rearrangement
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    Chapter 86 Dess–Martin periodinane oxidation
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    Chapter 87 Dieckmann condensation
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    Chapter 88 Diels–Alder reaction
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    Chapter 89 Dienone–phenol rearrangement
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    Chapter 90 Doebner quinoline synthesis
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    Chapter 91 Doebner–von Miller reaction
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    Chapter 92 Dötz reaction
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    Chapter 93 Dowd–Beckwith ring expansion
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    Chapter 94 Dudley reagent
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    Chapter 95 Erlenmeyer–Plöchl azlactone synthesis
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    Chapter 96 Eschenmoser’s salt
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    Chapter 97 Eschenmoser–Tanabe fragmentation
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    Chapter 98 Eschweiler–Clarke reductive alkylation of amines
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    Chapter 99 Evans aldol reaction
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    Chapter 100 Favorskii rearrangement
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    Chapter 101 Feist–Bénary furan synthesis
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    Chapter 104 Fiesselmann thiophene synthesis
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    Chapter 106 Fischer indole synthesis
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    Chapter 107 Fischer oxazole synthesis
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    Chapter 108 Fleming–Kumada oxidation
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    Chapter 109 Friedel–Crafts reaction
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    Chapter 110 Friedländer quinoline synthesis
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    Chapter 111 Fries rearrangement
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    Chapter 112 Fukuyama amine synthesis
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    Chapter 113 Fukuyama reduction
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    Chapter 114 Gabriel synthesis
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    Chapter 116 Gassman indole synthesis
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    Chapter 117 Gattermann–Koch reaction
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    Chapter 118 Gewald aminothiophene synthesis
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    Chapter 121 Gould–Jacobs reaction
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    Chapter 122 Grignard reaction
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    Chapter 125 Hajos–Wiechert reaction
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    Chapter 127 Hantzsch dihydropyridine synthesis
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    Chapter 130 Hegedus indole synthesis
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    Chapter 131 Hell–Volhard–Zelinsky reaction
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    Chapter 132 Henry nitroaldol reaction
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    Chapter 134 Hiyama cross-coupling reaction
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    Chapter 135 Hofmann elimination
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    Chapter 136 Hofmann rearrangement
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    Chapter 137 Hofmann–Löffler–Freytag reaction
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    Chapter 138 Horner–Wadsworth–Emmons reaction
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    Chapter 139 Houben–Hoesch reaction
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    Chapter 140 Hunsdiecker–Borodin reaction
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    Chapter 141 Jacobsen–Katsuki epoxidation
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    Chapter 142 Japp–Klingemann hydrazone synthesis
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    Chapter 143 Jones oxidation
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    Chapter 144 Julia–Kocienski olefination
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    Chapter 145 Julia–Lythgoe olefination
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    Chapter 146 Kahne glycosidation
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    Chapter 148 Knorr pyrazole synthesis
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    Chapter 149 Koch–Haaf carbonylation
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    Chapter 150 Koenig–Knorr glycosidation
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    Chapter 151 Kostanecki reaction
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    Chapter 152 Kröhnke pyridine synthesis
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    Chapter 153 Krapcho reaction
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    Chapter 154 Kumada cross-coupling reaction
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    Chapter 155 Lawesson’s reagent
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    Chapter 156 Leuckart–Wallach reaction
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    Chapter 158 Lossen rearrangement
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    Chapter 159 McFadyen–Stevens reduction
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    Chapter 160 McMurry coupling
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    Chapter 161 MacMillan catalyst
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    Chapter 163 Markovnikov’s rule
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    Chapter 165 Masamune–Roush conditions for the Horner–Emmons reaction
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    Chapter 166 Meerwein’s salt
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    Chapter 167 Meerwein–Ponndorf–Verley reduction
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    Chapter 168 Meisenheimer complex
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    Chapter 169 [1,2]-Meisenheimer rearrangement
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    Chapter 172 Meyer–Schuster rearrangement
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    Chapter 173 Michael addition
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    Chapter 174 Michaelis–Arbuzov phosphonate synthesis
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    Chapter 175 Midland reduction
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    Chapter 176 Minisci reaction
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    Chapter 177 Mislow–Evans rearrangement
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    Chapter 179 Miyaura borylation
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    Chapter 180 Moffatt oxidation
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    Chapter 181 Morgan–Walls reaction
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    Chapter 182 Mori–Ban indole synthesis
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    Chapter 184 Mukaiyama Michael addition
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    Chapter 185 Mukaiyama reagent
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    Chapter 186 Myers–Saito cyclization
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    Chapter 187 Nazarov cyclization
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    Chapter 188 Neber rearrangement
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    Chapter 189 Nef reaction
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    Chapter 190 Negishi cross-coupling reaction
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    Chapter 191 Nenitzescu indole synthesis
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    Chapter 192 Newman–Kwart rearrangement
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    Chapter 193 Nicholas reaction
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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 Nysted reagent
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    Chapter 198 Oppenauer oxidation
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    Chapter 199 Overman rearrangement
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    Chapter 200 Paal thiophene synthesis
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    Chapter 201 Paal–Knorr furan synthesis
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    Chapter 202 Paal–Knorr pyrrole synthesis
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    Chapter 203 Parham cyclization
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    Chapter 205 Paternó–Büchi reaction
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    Chapter 206 Pauson–Khand reaction
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    Chapter 208 Pechmann coumarin synthesis
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    Chapter 209 Perkin reaction
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    Chapter 210 Perkow vinyl phosphate synthesis
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    Chapter 211 Petasis reaction
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    Chapter 213 Peterson olefination
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    Chapter 214 Pictet–Gams isoquinoline synthesis
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    Chapter 215 Pictet–Spengler tetrahydroisoquinoline synthesis
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    Chapter 216 Pinacol rearrangement
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    Chapter 217 Pinner reaction
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    Chapter 218 Polonovski reaction
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    Chapter 219 Polonovski–Potier reaction
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    Chapter 220 Pomeranz–Fritsch reaction
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    Chapter 221 Pavorov reaction
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    Chapter 222 Prévost trans -dihydroxylation
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    Chapter 223 Prins reaction
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    Chapter 224 Pschorr cyclization
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    Chapter 225 Pummerer rearrangement
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    Chapter 226 Ramberg–Bäcklund reaction
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    Chapter 227 Reformatsky reaction
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    Chapter 228 Regitz diazo synthesis
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    Chapter 229 Reimer–Tiemann reaction
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    Chapter 230 Reissert reaction
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    Chapter 231 Reissert indole synthesis
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    Chapter 232 Ring-closing metathesis (RCM)
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    Chapter 233 Ritter reaction
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    Chapter 234 Robinson annulation
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    Chapter 237 Rosenmund reduction
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    Chapter 239 Rupe rearrangement
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    Chapter 240 Saegusa oxidation
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    Chapter 241 Sakurai allylation reaction
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    Chapter 242 Sandmeyer reaction
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    Chapter 243 Schiemann reaction
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    Chapter 244 Schmidt rearrangement
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    Chapter 245 Schmidt’s trichloroacetimidate glycosidation
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    Chapter 246 Scholl reaction
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    Chapter 247 Shapiro reaction
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    Chapter 248 Sharpless asymmetric amino-hydroxylation
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    Chapter 249 Sharpless asymmetric dihydroxylation
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    Chapter 250 Sharpless asymmetric epoxidation
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    Chapter 251 Sharpless olefin synthesis
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    Chapter 252 Shi asymmetric epoxidation
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    Chapter 253 Simmons–Smith reaction
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    Chapter 254 Skraup quinoline synthesis
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    Chapter 256 Sommelet reaction
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    Chapter 257 Sommelet–Hauser rearrangement
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    Chapter 258 Sonogashira reaction
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    Chapter 259 Staudinger ketene cycloaddition
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    Chapter 260 Staudinger reduction
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    Chapter 261 Stetter reaction
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    Chapter 263 Still–Gennari phosphonate reaction
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    Chapter 264 Stille coupling
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    Chapter 265 Stille–Kelly rea ction
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    Chapter 266 Stobbe condensation
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    Chapter 268 Strecker amino acid synthesis
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    Chapter 271 Takai reaction
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    Chapter 272 Tebbe reagent
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    Chapter 273 TEMPO oxidation
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    Chapter 274 Thorpe–Ziegler reaction
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    Chapter 275 Tsuji–Trost reaction
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    Chapter 276 Ugi reaction
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    Chapter 278 van Leusen oxazole synthesis
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    Chapter 279 Vilsmeier–Haack reaction
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    Chapter 280 Vinylcyclopropane–cyclopentene rearrangement
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    Chapter 281 von Braun reaction
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    Chapter 283 Wagner–Meerwein rearrangement
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    Chapter 284 Weiss–Cook condensation
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    Chapter 285 Wharton reaction
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    Chapter 286 Williamson ether synthesis
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    Chapter 287 Willgerodt–Kindler reaction
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    Chapter 288 Wittig reaction
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    Chapter 289 [1,2]-Wittig rearrangement
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    Chapter 290 [2,3]-Wittig rearrangement
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    Chapter 291 Wohl–Ziegler reaction
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    Chapter 292 Wolff rearrangement
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    Chapter 293 Wolff–Kishner reduction
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    Chapter 294 Woodward cis -dihydroxylation
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    Chapter 295 Yamaguchi esterification
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    Chapter 296 Zaitsev’s elimination rule
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    Chapter 297 Zhang enyne cycloisomerization
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    Chapter 299 Zincke reaction
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    Chapter 300 Zinin benzidine (semidne) rearrangement
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Title
Name Reactions : A Collection of Detailed Mechanisms and Synthetic Applications Fifth Edition
Published by
Springer Science & Business Media, January 2014
DOI 10.1007/978-3-319-03979-4
ISBNs
978-3-31-903979-4, 978-3-31-903978-7, 978-3-31-937431-4
Authors

Li, Jie Jack, Jie Jack Li

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The data shown below were compiled from readership statistics for 182 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
India 1 <1%
United States 1 <1%
Unknown 180 99%

Demographic breakdown

Readers by professional status Count As %
Student > Master 43 24%
Student > Ph. D. Student 32 18%
Student > Bachelor 30 16%
Researcher 13 7%
Student > Doctoral Student 9 5%
Other 18 10%
Unknown 37 20%
Readers by discipline Count As %
Chemistry 116 64%
Biochemistry, Genetics and Molecular Biology 7 4%
Chemical Engineering 7 4%
Pharmacology, Toxicology and Pharmaceutical Science 4 2%
Agricultural and Biological Sciences 3 2%
Other 7 4%
Unknown 38 21%