Verfügbarkeit: Comprehensive organic name reactions and reagents

Comprehensive organic name reactions and reagents: 1

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Bibliographische Detailangaben
1. Verfasser:	Wang, Zerong (VerfasserIn)
Format:	Buch
Sprache:	English
Veröffentlicht:	Hoboken, NJ Wiley (2009)
Online-Zugang:	Inhaltsverzeichnis
Beschreibung:	XLIX, 1304 S. Ill., graph. Darst.
ISBN:	9780470286623

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300			\|a XLIX, 1304 S. \|b Ill., graph. Darst.
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Datensatz im Suchindex

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adam_text	Contents Preface ................................................................ xxix Acknowledgments ..................................................... xxxi Autobiography ....................................................... xxxiii Chemical Abbreviations .............................................. xxxv PART ONE 1. Abnormal Claisen Rearrangement ..................................... 1 2. Acetoacetic Ester Condensation ........................................ 5 3. Acetoacetic Ester Synthesis ............................................. 9 4. Acyloin Condensation ................................................. 13 5. Acyloin Rearrangement ............................................... 18 6. Adkins Catalyst ...................................................... 21 7. AinJey and King Synthesis ............................................ 25 8. Akabori Amino Acid Reaction ........................................ 29 9. Albright-Goldman Oxidation ......................................... 33 10. Alder Ene Reaction ................................................... 37 11. Alder-Rickert Reaction ............................................... 41 12. Aldol Reaction and Aldol Condensation ............................... 45 v VÍ CONTENTS 13. Algar-Flynn-Oyamada (AFO) Reaction................................ 52 14. Alkene Metathesis .................................................... 57 15. Allan-Robinson Condensation ......................................... 64 16. Ally lie Rearrangement ................................................ 68 17. Amadori Rearrangement ............................................. 74 18. Andrussow Process ................................................... 80 19. Angeli-Remini Reaction ............................................... 83 20. ANRORC Rearrangement ............................................ 87 21. Anschiitz Anthracene Synthesis ....................................... 91 22. Appel Reaction ....................................................... 95 23. Arens- van Dorp Reaction ............................................ 100 24. Arndt-Eistert Synthesis .............................................. 103 25. Asinger Reaction .................................................... 107 26. Aston-Greenburg Rearrangement .................................... Ill 27. Atherton-Todd Reaction ............................................. 114 28. Auwers-Skita Rule ................................................... 119 29. Aza-Claisen Rearrangement ......................................... 123 30. Baddeley Isomerization .............................................. 128 31. Baeyer Diarylmethane Synthesis ..................................... 132 32. Baeyer-Drewson Reaction ............................................ 136 33. Baeyer Indole Synthesis .............................................. 140 34. Baeyer Oxindole Synthesis ........................................... 144 35. Baeyer Pyridine Synthesis ........................................... 147 36. Baeyer- Villiger Oxidation ............................................ 150 37. Bailey Peptide Synthesis ............................................. 156 38. Bakelite Process ..................................................... 160 39. Baker-Ollis Sydnones Synthesis ...................................... 164 40. Baker-Venkataraman Rearrangement ................................ 168 41. Ball-Goodwin-Morton Oxidation ..................................... 173 42. Bally-Scholl Reaction ................................................ 176 43. Balsohn Alkylation .................................................. 181 44. Balz-Schiemann Reaction ............................................ 185 CONTENTS VU 45. Bamberger Rearrangement .......................................... 191 46. Bamford-Stevens Reaction ........................................... 195 47. Barbier Reaction .................................................... 202 48. Barbier-Wieland Degradation........................................ 210 49. Bardhan Sengupta Synthesis ......................................... 215 50. Bargellini Condensation ............................................. 220 51. Bart Reaction ....................................................... 224 52. Bartoli Indole Synthesis.............................................. 228 53. Barton Decarboxylation ............................................. 232 54. Barton Deoxygenation ............................................... 237 55. Barton Reaction ..................................................... 245 56. Barton-Kellogg Olefìnation .......................................... 249 57. Barton-Zard Pyrrole Synthesis ....................................... 254 58. Batcho-Leimgruber Indole Synthesis ................................. 258 59. Baudisch Reaction ................................................... 263 60. Baumann-Fromm Thiophene Synthesis ............................... 267 61. Baumgarten α -Amino Ketone Synthesis .............................. 271 62. Baylis-Hillman Reaction ............................................. 275 63. Béchamp Reduction ................................................. 284 64. Beckmann Rearrangement and Beckmann Fragmentation ............ 288 65. Bedoukian Halogenation ............................................. 296 66. Béhal-Sommelet Rearrangement ..................................... 300 67. Beirut Reaction ..................................................... 303 68. Belluš-Claisen Rearrangement ....................................... 307 69. Bénary Reaction ..................................................... 311 70. Benkeser Reduction ................................................. 315 71. Benzidine Rearrangement ........................................... 320 72. Benzilic Acid Rearrangement ........................................ 326 73. Benzoin Condensation ............................................... 331 74. Bergius Process ...................................................... 337 75. Bergman Cyclization ................................................ 341 76. Bergmann Degradation .............................................. 349 VIH CONTENTS 77. Bergmann-Stern Azlactone Synthesis................................. 353 78. Bergmann-Zervas Peptide Synthesis .................................. 358 79. Bernthsen Reaction .................................................. 362 80. Berti Olefínation .................................................... 366 81. Bertram-Walbaum Reaction......................................... 370 82. Betti Reaction ....................................................... 374 83. Biginelli Reaction .................................................... 379 84. Birch Reduction ..................................................... 387 85. Birckenbach-Goubeau Halogenation ................................. 398 86. Birnbaum-Simonini Reaction ........................................ 402 87. Bischler Reaction .................................................... 406 88. Bischler-Napieralski Isoquinoline Synthesis ........................... 410 89. Black Rearrangement ............................................... 416 90. Blaise Ketone Synthesis .............................................. 420 91. Blaise Reaction ...................................................... 424 92. Blanc Chloromethylation ............................................ 429 93. BlancRule .......................................................... 433 94. Blomquist Cyclic Ketone Synthesis ................................... 437 95. Bobbitt Reaction .................................................... 441 96. Bodroux Amide Synthesis ............................................ 445 97. Bodroux-Chichibabin Reaction ...................................... 448 98. Böeseken Oxidation ................................................. 452 99. Bogert-Cook Synthesis ............................................... 455 100. Bonn-Schmidt Reaction .............................................. 459 101. Boord Olefin Synthesis ............................................... 463 102. Borsche-Berkhout Reaction .......................................... 468 103. Borsche-Drechsel Reaction ........................................... 471 104. Borsche-Koelsch Cinnoline Synthesis ................................. 474 105. Bougault Reaction ................................................... 478 106. Boulton-Katritzky Rearrangement ................................... 482 107. Bourgel Alkyne Synthesis ............................................ 487 108. Bouveault Aldehyde Synthesis ........................................ 490 CONTENTS ¡Χ 109. Bouveault-Blanc Reduction .......................................... 493 110. Boyland-Sims Oxidation ............................................. 497 111. Bradsher Cyclization ................................................ 501 112. Bradsher Cycloaddition ............................................. 506 113. Bradsher Pyridinium Salt Synthesis .................................. 511 114. Brandi-Guarna Reaction ............................................. 515 115. Breckpot /S-Lactam Synthesis ........................................ 521 116. BredťsRule ......................................................... 525 117. Brook Rearrangement ............................................... 529 118. Brown Hydroboration ............................................... 536 119. Bruckner Isoquinoline Synthesis ..................................... 544 120. Bucherer Carbazole Synthesis ........................................ 549 121. Bucherer Reaction ................................................... 553 122. Bucherer-Bergs Hydantoin Synthesis ................................. 557 123. Büchner Ring Expansion ............................................ 562 124. Biichner-Curtius-Schlotterbeck Reaction ............................. 567 125. Buchwald Indoline Synthesis ......................................... 570 126. Buchwald-Hartwig Amination ....................................... 575 127. Burton Trifluoromethylation ......................................... 582 128. Cadogan-Sundberg Indole Synthesis ................................. 585 129. Caglioti Reaction .................................................... 589 130. Cahours-Hofmann Reaction .....................................----- 595 131. Camps Reaction ..................................................... 598 132. Cannizzaro Reaction ................................................ 602 133. Carboni-Lindsey Reaction ........................................... 606 134. Carroll Rearrangement .............................................. 611 135. Castro Indole Synthesis .............................................. 616 136. Castro-Stephens Coupling ........................................... 619 137. Chan Rearrangement ................................................ 624 138. Chapman Rearrangement ........................................... 627 139. Chichibabin Amination.............................................. 631 140. Chichibabin Pyridine Synthesis ...................................... 635 X CONTENTS 141. Chretien-Longi Reaction ............................................. 639 142. Chugaev Reaction ................................................... 642 143. Ciamician-Dennstedt Reaction ....................................... 646 144. Claisen Rearrangement .............................................. 649 145. Claisen-Schmidt Condensation ....................................... 660 146. Clauson-Kaas Reaction .............................................. 665 147. Clay-Kinnear-Perren Condensation .................................. 669 148. Clayton-Jensen Chlorophosphonation ................................ 673 149. Clemmensen Reduction .............................................. 677 150. Cohen Reductive Lithiation .......................................... 683 151. Combes Quinoline Synthesis ......................................... 688 152. Conrad-Limpach Quinoline Synthesis ................................ 692 153. Cope Elimination .................................................... 697 154. Cope Rearrangement ................................................ 702 155. Corey-Bakshi-Shibata Reduction ..................................... 709 156. Corey-Chaykovsky Epoxidation ...................................... 713 157. Corey-Fuchs Reaction ............................................... 717 158. Corey-Gilman-Ganem Oxidation ..................................... 722 159. Corey-Kim Oxidation ................................................ 726 160. Corey-Kwiatkowski Reaction ........................................ 730 161. Corey-Link Reaction ................................................ 734 162. Corey-Schmidt Oxidation ............................................ 738 163. Corey-Suggs Oxidation .............................................. 742 164. Corey-Winter Olefination ............................................ 746 165. Cornforth Rearrangement ........................................... 750 166. Craig 2-Bromo-Pyridine Synthesis ................................... 753 167. Cram sRule ........................................................ 756 168. Criegee Glycol Oxidation ............................................ 761 169. Criegee Ozonolysis .................................................. 765 170. Criegee Rearrangement .............................................. 770 171. Crum-Brown-Gibson Substitution Rule .............................. 775 172. Curtius Rearrangement .............................................. 780 CONTENTS Xl 173. [m+n(+... )] Cycloaddition........................................... 786 174. [2+2] Cycloaddition .................................................. 819 175. Dakin Reaction ...................................................... 829 176. Dakin- West Reaction ................................................ 832 177. Danheiser Annulation ............................................... 837 178. Darzens Condensation ............................................... 841 179. Darzens Halogenation ............................................... 846 180. Darzens Olefin Acylation ............................................ 848 181. Darzens-Nenitzescu Reaction ........................................ 851 182. Davidson Oxazole Cyclization ........................................ 855 183. de Mayo Reaction ................................................... 858 184. Decker-Becker Secondary Amine Synthesis ........................... 862 185. Delépine Reaction ................................................... 865 186. Demjanov Rearrangement ........................................... 868 187. Dess-Martin Periodinane Oxidation .................................. 871 188. D-Homo Rearrangement ............................................. 877 189. Dieckmann Condensation ............................................ 881 190. Diels-Alder Reaction ................................................. 886 191. Diels-Reese Reaction ................................................. 892 192. Dienol-Benzene Rearrangement ...................................... 897 193. Dienone-Phenol Rearrangement ...................................... 900 194. Dimroth Rearrangement ............................................. 905 195. Di- Π -Methane Rearrangement ....................................... 910 196. 1,3-Dipolar Cycloaddition ............................................ 916 197. Doebner Reaction ................................................... 921 198. Doebner-Miller Reaction ............................................. 924 199. Doering-Moore-Skattebol Reaction ................................... 930 200. Dötz Benzannulation ................................................ 934 201. Dowd-Beckwith Ring Expansion ..................................... 939 202. DuffReaction ....................................................... 942 203. Dutt-Wormall Reaction .............................................. 946 204. Eastwood Olefination ................................................ 949 XU CONTENTS 205. Eder Reaction ....................................................... 952 206. Edman Degradation ................................................. 954 207. Eglinton Coupling ................................................... 959 208. Ehrlich-Sachs Reaction .............................................. 964 209. Einhorn Acylation ................................................... 967 210. Einhorn-Brunner Reaction ........................................... 971 211. Eisleb Alkylation .................................................... 974 212. Elbs Persulfate Oxidation ............................................ 977 213. Elbs Reaction ....................................................... 982 214. Eltekoff Hydrolysis .................................................. 986 215. Emde Degradation .................................................. 989 216. Emmert Reaction .................................................... 993 217. Erlenmeyer-Plöchl Aziactone Synthesis ............................... 997 218. Eschenmoser Coupling ............................................. 1001 219. Eschenmoser Fragmentation ........................................ 1005 220. Eschweiler-Clarke Methylation ..................................... 1009 221. Ester Pyrolysis ..................................................... 1013 222. Étard Reaction ..................................................... 1017 223. Evans Aldol Reaction ............................................... 1021 224. Favorskii Rearrangement ........................................... 1026 225. Favorskii-Babayan Reaction ........................................ 1032 226. Feist-Bénary Reaction .............................................. 1036 227. Fenton Reaction .................................................... 1041 228. Ferrier Reaction ................................................... 1046 229. Ferrier-II Rearrangement .......................................... 1051 230. Fétizon Oxidation .................................................. 1055 231. Finkelstein Reaction ................................................ 1060 232. Fischer Carbene Complexes ........................................ 1064 233. Fischer Indole Synthesis ............................................ 1069 234. Fischer Oxazole Synthesis .......................................... 1076 235. Fischer Phenylhydrazine Synthesis .................................. 1080 236. Fischer Phenylhydrazone and Osazone Synthesis .................... 1083 CONTENTS ХІІІ 237. Fischer-Helferich Glycosylation..................................... 1088 238. Fischer-Hepp Rearrangement ....................................... 1091 239. Fischer-Speier Esterifkation........................................ 1095 240. Fischer-Tropsch Synthesis .......................................... 1098 241. Fleming-Tamao Oxidation .......................................... 1103 242. Flood Reaction ..................................................... 1107 243. Forster Reaction ................................................... 1110 244. Franchimont Condensation ......................................... 1113 245. Frankland Reaction ................................................ 1116 246. Fráter-Seebach Alkylation .......................................... 1120 247. Freund Reaction ................................................... 1123 248. Friedel-Crafts Acylation............................................ 1126 249. Friedel-Crafts Alkylation ........................................... 1131 250. Friedländer Condensation.......................................... 1137 251. Fries Rearrangement ............................................... 1143 252. Fritsch-Buttenberg-Wiechell Rearrangement ........................ 1151 253. Fujimoto-Belleau Reaction .......................................... 1155 254. Fukuyama Amine Synthesis ......................................... 1159 255. Fukuyama Indole Synthesis ......................................... 1164 256. Fürstner Indole Synthesis ........................................... 1170 257. Gabriel Primary Amine Synthesis ................................... 1176 258. Gabriel Reaction ................................................... 1180 259. Gabriel-Colman Rearrangement .................................... 1183 260. Garner Aldehyde ................................................... 1187 261. Gassman Indole Synthesis .......................................... 1191 262. Gassman Oxindole Synthesis ........................................ 1194 263. Gassman Reaction .................................................. 1198 264. Gattermann Aldehyde Synthesis .................................... 1202 265. Gattermann Reaction ............................................... 1206 266. Gattermann-Koch Formylation ..................................... 1209 267. Gewald Reaction ................................................... 1213 268. Ghosez Cyclization ................................................. 1217 XIV CONTENTS 269. Ghosez Keteniminium-Olefin Cyclization ............................ 1221 270. Gibbs-Wohl Naphthalene Oxidation................................. 1227 271. Gilman-Cason Ketone Synthesis .................................... 1230 272. Gilman-Speeter Reaction ........................................... 1234 273. Gomberg Free Radical Reaction .................................... 1238 274. Gomberg-Bachmann Pinacol Synthesis .............................. 1245 275. Gomberg-Bachmann Reaction ...................................... 1248 276. Gould-Jacobs Reaction ............................................. 1252 277. Graebe-UHmann Synthesis .......................................... 1256 278. Gränacher Synthesis ............................................... 1260 279. Gribble Reductive Amination....................................... 1264 280. Griess Diazotization ................................................ 1267 281. Grignard Degradation .............................................. 1271 282. Grignard Reaction ................................................. 1273 283. Grob Fragmentation ............................................... 1279 284. Grosheintz-Fischer-Reissert Aldehyde Synthesis ..................... 1284 285. Grundmann Aldehyde Synthesis .................................... 1288 286. Gryszkiewicz-Trochimowski and Mccombie Fluorination ............ 1291 287. Guareschi Reaction ................................................. 1294 288. Guerbet Condensation .............................................. 1298 289. Gutknecht Condensation ........................................... 1302
adam_txt	Contents Preface . xxix Acknowledgments . xxxi Autobiography . xxxiii Chemical Abbreviations . xxxv PART ONE 1. Abnormal Claisen Rearrangement . 1 2. Acetoacetic Ester Condensation . 5 3. Acetoacetic Ester Synthesis . 9 4. Acyloin Condensation . 13 5. Acyloin Rearrangement . 18 6. Adkins Catalyst . 21 7. AinJey and King Synthesis . 25 8. Akabori Amino Acid Reaction . 29 9. Albright-Goldman Oxidation . 33 10. Alder Ene Reaction . 37 11. Alder-Rickert Reaction . 41 12. Aldol Reaction and Aldol Condensation . 45 v VÍ CONTENTS 13. Algar-Flynn-Oyamada (AFO) Reaction. 52 14. Alkene Metathesis . 57 15. Allan-Robinson Condensation . 64 16. Ally lie Rearrangement . 68 17. Amadori Rearrangement . 74 18. Andrussow Process . 80 19. Angeli-Remini Reaction . 83 20. ANRORC Rearrangement . 87 21. Anschiitz Anthracene Synthesis . 91 22. Appel Reaction . 95 23. Arens- van Dorp Reaction . 100 24. Arndt-Eistert Synthesis . 103 25. Asinger Reaction . 107 26. Aston-Greenburg Rearrangement . Ill 27. Atherton-Todd Reaction . 114 28. Auwers-Skita Rule . 119 29. Aza-Claisen Rearrangement . 123 30. Baddeley Isomerization . 128 31. Baeyer Diarylmethane Synthesis . 132 32. Baeyer-Drewson Reaction . 136 33. Baeyer Indole Synthesis . 140 34. Baeyer Oxindole Synthesis . 144 35. Baeyer Pyridine Synthesis . 147 36. Baeyer- Villiger Oxidation . 150 37. Bailey Peptide Synthesis . 156 38. Bakelite Process . 160 39. Baker-Ollis Sydnones Synthesis . 164 40. Baker-Venkataraman Rearrangement . 168 41. Ball-Goodwin-Morton Oxidation . 173 42. Bally-Scholl Reaction . 176 43. Balsohn Alkylation . 181 44. Balz-Schiemann Reaction . 185 CONTENTS VU 45. Bamberger Rearrangement . 191 46. Bamford-Stevens Reaction . 195 47. Barbier Reaction . 202 48. Barbier-Wieland Degradation. 210 49. Bardhan Sengupta Synthesis . 215 50. Bargellini Condensation . 220 51. Bart Reaction . 224 52. Bartoli Indole Synthesis. 228 53. Barton Decarboxylation . 232 54. Barton Deoxygenation . 237 55. Barton Reaction . 245 56. Barton-Kellogg Olefìnation . 249 57. Barton-Zard Pyrrole Synthesis . 254 58. Batcho-Leimgruber Indole Synthesis . 258 59. Baudisch Reaction . 263 60. Baumann-Fromm Thiophene Synthesis . 267 61. Baumgarten α -Amino Ketone Synthesis . 271 62. Baylis-Hillman Reaction . 275 63. Béchamp Reduction . 284 64. Beckmann Rearrangement and Beckmann Fragmentation . 288 65. Bedoukian Halogenation . 296 66. Béhal-Sommelet Rearrangement . 300 67. Beirut Reaction . 303 68. Belluš-Claisen Rearrangement . 307 69. Bénary Reaction . 311 70. Benkeser Reduction . 315 71. Benzidine Rearrangement . 320 72. Benzilic Acid Rearrangement . 326 73. Benzoin Condensation . 331 74. Bergius Process . 337 75. Bergman Cyclization . 341 76. Bergmann Degradation . 349 VIH CONTENTS 77. Bergmann-Stern Azlactone Synthesis. 353 78. Bergmann-Zervas Peptide Synthesis . 358 79. Bernthsen Reaction . 362 80. Berti Olefínation . 366 81. Bertram-Walbaum Reaction. 370 82. Betti Reaction . 374 83. Biginelli Reaction . 379 84. Birch Reduction . 387 85. Birckenbach-Goubeau Halogenation . 398 86. Birnbaum-Simonini Reaction . 402 87. Bischler Reaction . 406 88. Bischler-Napieralski Isoquinoline Synthesis . 410 89. Black Rearrangement . 416 90. Blaise Ketone Synthesis . 420 91. Blaise Reaction . 424 92. Blanc Chloromethylation . 429 93. BlancRule . 433 94. Blomquist Cyclic Ketone Synthesis . 437 95. Bobbitt Reaction . 441 96. Bodroux Amide Synthesis . 445 97. Bodroux-Chichibabin Reaction . 448 98. Böeseken Oxidation . 452 99. Bogert-Cook Synthesis . 455 100. Bonn-Schmidt Reaction . 459 101. Boord Olefin Synthesis . 463 102. Borsche-Berkhout Reaction . 468 103. Borsche-Drechsel Reaction . 471 104. Borsche-Koelsch Cinnoline Synthesis . 474 105. Bougault Reaction . 478 106. Boulton-Katritzky Rearrangement . 482 107. Bourgel Alkyne Synthesis . 487 108. Bouveault Aldehyde Synthesis . 490 CONTENTS ¡Χ 109. Bouveault-Blanc Reduction . 493 110. Boyland-Sims Oxidation . 497 111. Bradsher Cyclization . 501 112. Bradsher Cycloaddition . 506 113. Bradsher Pyridinium Salt Synthesis . 511 114. Brandi-Guarna Reaction . 515 115. Breckpot /S-Lactam Synthesis . 521 116. BredťsRule . 525 117. Brook Rearrangement . 529 118. Brown Hydroboration . 536 119. Bruckner Isoquinoline Synthesis . 544 120. Bucherer Carbazole Synthesis . 549 121. Bucherer Reaction . 553 122. Bucherer-Bergs Hydantoin Synthesis . 557 123. Büchner Ring Expansion . 562 124. Biichner-Curtius-Schlotterbeck Reaction . 567 125. Buchwald Indoline Synthesis . 570 126. Buchwald-Hartwig Amination . 575 127. Burton Trifluoromethylation . 582 128. Cadogan-Sundberg Indole Synthesis . 585 129. Caglioti Reaction . 589 130. Cahours-Hofmann Reaction .----- 595 131. Camps Reaction . 598 132. Cannizzaro Reaction . 602 133. Carboni-Lindsey Reaction . 606 134. Carroll Rearrangement . 611 135. Castro Indole Synthesis . 616 136. Castro-Stephens Coupling . 619 137. Chan Rearrangement . 624 138. Chapman Rearrangement . 627 139. Chichibabin Amination. 631 140. Chichibabin Pyridine Synthesis . 635 X CONTENTS 141. Chretien-Longi Reaction . 639 142. Chugaev Reaction . 642 143. Ciamician-Dennstedt Reaction . 646 144. Claisen Rearrangement . 649 145. Claisen-Schmidt Condensation . 660 146. Clauson-Kaas Reaction . 665 147. Clay-Kinnear-Perren Condensation . 669 148. Clayton-Jensen Chlorophosphonation . 673 149. Clemmensen Reduction . 677 150. Cohen Reductive Lithiation . 683 151. Combes Quinoline Synthesis . 688 152. Conrad-Limpach Quinoline Synthesis . 692 153. Cope Elimination . 697 154. Cope Rearrangement . 702 155. Corey-Bakshi-Shibata Reduction . 709 156. Corey-Chaykovsky Epoxidation . 713 157. Corey-Fuchs Reaction . 717 158. Corey-Gilman-Ganem Oxidation . 722 159. Corey-Kim Oxidation . 726 160. Corey-Kwiatkowski Reaction . 730 161. Corey-Link Reaction . 734 162. Corey-Schmidt Oxidation . 738 163. Corey-Suggs Oxidation . 742 164. Corey-Winter Olefination . 746 165. Cornforth Rearrangement . 750 166. Craig 2-Bromo-Pyridine Synthesis . 753 167. Cram'sRule . 756 168. Criegee Glycol Oxidation . 761 169. Criegee Ozonolysis . 765 170. Criegee Rearrangement . 770 171. Crum-Brown-Gibson Substitution Rule . 775 172. Curtius Rearrangement . 780 CONTENTS Xl' 173. [m+n(+. )] Cycloaddition. 786 174. [2+2] Cycloaddition . 819 175. Dakin Reaction . 829 176. Dakin- West Reaction . 832 177. Danheiser Annulation . 837 178. Darzens Condensation . 841 179. Darzens Halogenation . 846 180. Darzens Olefin Acylation . 848 181. Darzens-Nenitzescu Reaction . 851 182. Davidson Oxazole Cyclization . 855 183. de Mayo Reaction . 858 184. Decker-Becker Secondary Amine Synthesis . 862 185. Delépine Reaction . 865 186. Demjanov Rearrangement . 868 187. Dess-Martin Periodinane Oxidation . 871 188. D-Homo Rearrangement . 877 189. Dieckmann Condensation . 881 190. Diels-Alder Reaction . 886 191. Diels-Reese Reaction . 892 192. Dienol-Benzene Rearrangement . 897 193. Dienone-Phenol Rearrangement . 900 194. Dimroth Rearrangement . 905 195. Di- Π -Methane Rearrangement . 910 196. 1,3-Dipolar Cycloaddition . 916 197. Doebner Reaction . 921 198. Doebner-Miller Reaction . 924 199. Doering-Moore-Skattebol Reaction . 930 200. Dötz Benzannulation . 934 201. Dowd-Beckwith Ring Expansion . 939 202. DuffReaction . 942 203. Dutt-Wormall Reaction . 946 204. Eastwood Olefination . 949 XU CONTENTS 205. Eder Reaction . 952 206. Edman Degradation . 954 207. Eglinton Coupling . 959 208. Ehrlich-Sachs Reaction . 964 209. Einhorn Acylation . 967 210. Einhorn-Brunner Reaction . 971 211. Eisleb Alkylation . 974 212. Elbs Persulfate Oxidation . 977 213. Elbs Reaction . 982 214. Eltekoff Hydrolysis . 986 215. Emde Degradation . 989 216. Emmert Reaction . 993 217. Erlenmeyer-Plöchl Aziactone Synthesis . 997 218. Eschenmoser Coupling . 1001 219. Eschenmoser Fragmentation . 1005 220. Eschweiler-Clarke Methylation . 1009 221. Ester Pyrolysis . 1013 222. Étard Reaction . 1017 223. Evans Aldol Reaction . 1021 224. Favorskii Rearrangement . 1026 225. Favorskii-Babayan Reaction . 1032 226. Feist-Bénary Reaction . 1036 227. Fenton Reaction . 1041 228. Ferrier Reaction . 1046 229. Ferrier-II Rearrangement . 1051 230. Fétizon Oxidation . 1055 231. Finkelstein Reaction . 1060 232. Fischer Carbene Complexes . 1064 233. Fischer Indole Synthesis . 1069 234. Fischer Oxazole Synthesis . 1076 235. Fischer Phenylhydrazine Synthesis . 1080 236. Fischer Phenylhydrazone and Osazone Synthesis . 1083 CONTENTS ХІІІ 237. Fischer-Helferich Glycosylation. 1088 238. Fischer-Hepp Rearrangement . 1091 239. Fischer-Speier Esterifkation. 1095 240. Fischer-Tropsch Synthesis . 1098 241. Fleming-Tamao Oxidation . 1103 242. Flood Reaction . 1107 243. Forster Reaction . 1110 244. Franchimont Condensation . 1113 245. Frankland Reaction . 1116 246. Fráter-Seebach Alkylation . 1120 247. Freund Reaction . 1123 248. Friedel-Crafts Acylation. 1126 249. Friedel-Crafts Alkylation . 1131 250. Friedländer Condensation. 1137 251. Fries Rearrangement . 1143 252. Fritsch-Buttenberg-Wiechell Rearrangement . 1151 253. Fujimoto-Belleau Reaction . 1155 254. Fukuyama Amine Synthesis . 1159 255. Fukuyama Indole Synthesis . 1164 256. Fürstner Indole Synthesis . 1170 257. Gabriel Primary Amine Synthesis . 1176 258. Gabriel Reaction . 1180 259. Gabriel-Colman Rearrangement . 1183 260. Garner Aldehyde . 1187 261. Gassman Indole Synthesis . 1191 262. Gassman Oxindole Synthesis . 1194 263. Gassman Reaction . 1198 264. Gattermann Aldehyde Synthesis . 1202 265. Gattermann Reaction . 1206 266. Gattermann-Koch Formylation . 1209 267. Gewald Reaction . 1213 268. Ghosez Cyclization . 1217 XIV CONTENTS 269. Ghosez Keteniminium-Olefin Cyclization . 1221 270. Gibbs-Wohl Naphthalene Oxidation. 1227 271. Gilman-Cason Ketone Synthesis . 1230 272. Gilman-Speeter Reaction . 1234 273. Gomberg Free Radical Reaction . 1238 274. Gomberg-Bachmann Pinacol Synthesis . 1245 275. Gomberg-Bachmann Reaction . 1248 276. Gould-Jacobs Reaction . 1252 277. Graebe-UHmann Synthesis . 1256 278. Gränacher Synthesis . 1260 279. Gribble Reductive Amination. 1264 280. Griess Diazotization . 1267 281. Grignard Degradation . 1271 282. Grignard Reaction . 1273 283. Grob Fragmentation . 1279 284. Grosheintz-Fischer-Reissert Aldehyde Synthesis . 1284 285. Grundmann Aldehyde Synthesis . 1288 286. Gryszkiewicz-Trochimowski and Mccombie Fluorination . 1291 287. Guareschi Reaction . 1294 288. Guerbet Condensation . 1298 289. Gutknecht Condensation . 1302
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spelling	Wang, Zerong Verfasser aut Comprehensive organic name reactions and reagents 1 Zerong Wang Hoboken, NJ Wiley (2009) XLIX, 1304 S. Ill., graph. Darst. txt rdacontent n rdamedia nc rdacarrier (DE-604)BV035164063 1 Digitalisierung UB Bayreuth application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=016971137&sequence=000002&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis
spellingShingle	Wang, Zerong Comprehensive organic name reactions and reagents
title	Comprehensive organic name reactions and reagents
title_auth	Comprehensive organic name reactions and reagents
title_exact_search	Comprehensive organic name reactions and reagents
title_exact_search_txtP	Comprehensive organic name reactions and reagents
title_full	Comprehensive organic name reactions and reagents 1 Zerong Wang
title_fullStr	Comprehensive organic name reactions and reagents 1 Zerong Wang
title_full_unstemmed	Comprehensive organic name reactions and reagents 1 Zerong Wang
title_short	Comprehensive organic name reactions and reagents
title_sort	comprehensive organic name reactions and reagents
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