Holdings: Name reactions :: THWS Bibkatalog

Name reactions: a collection of detailed reaction mechanisms

Saved in:

Bibliographic Details
Main Author:	Li, Jie Jack 1964- (Author)
Format:	Book
Language:	English
Published:	Berlin [u.a.] Springer 2003
Edition:	2. ed.
Subjects:	Chemische reacties Chimie organique Naamgeving Organische chemie Organische verbindingen Reactiemechanismen (chemie) Reações químicas Réactions organiques (Chimie) Chemical reactions Chemistry, Organic Organische Chemie Reaktionsmechanismus Namensreaktion Wörterbuch
Online Access:	Inhaltsverzeichnis
Physical Description:	XVIII, 465 S.
ISBN:	3540402039

Staff View

MARC


LEADER	00000nam a2200000 c 4500
001	BV017258850
003	DE-604
005	20041026
007	t
008	030624s2003 gw \|\|\|\| 00\|\|\| eng d
016	7		\|a 967883784 \|2 DE-101
020			\|a 3540402039 \|9 3-540-40203-9
035			\|a (OCoLC)52911268
035			\|a (DE-599)BVBBV017258850
040			\|a DE-604 \|b ger \|e rakddb
041	0		\|a eng
044			\|a gw \|c DE
049			\|a DE-29T \|a DE-19 \|a DE-703 \|a DE-11
050		0	\|a QD291
082	0		\|a 547.2 \|2 21
084			\|a VK 5503 \|0 (DE-625)147401:256 \|2 rvk
084			\|a VK 6003 \|0 (DE-625)147413:256 \|2 rvk
100	1		\|a Li, Jie Jack \|d 1964- \|e Verfasser \|0 (DE-588)123481848 \|4 aut
245	1	0	\|a Name reactions \|b a collection of detailed reaction mechanisms \|c Jie Jack Li
250			\|a 2. ed.
264		1	\|a Berlin [u.a.] \|b Springer \|c 2003
300			\|a XVIII, 465 S.
336			\|b txt \|2 rdacontent
337			\|b n \|2 rdamedia
338			\|b nc \|2 rdacarrier
650		7	\|a Chemische reacties \|2 gtt
650		4	\|a Chimie organique
650		7	\|a Naamgeving \|2 gtt
650		7	\|a Organische chemie \|2 gtt
650		7	\|a Organische verbindingen \|2 gtt
650		7	\|a Reactiemechanismen (chemie) \|2 gtt
650		7	\|a Reações químicas \|2 larpcal
650		4	\|a Réactions organiques (Chimie)
650		4	\|a Chemical reactions
650		4	\|a Chemistry, Organic
650	0	7	\|a Organische Chemie \|0 (DE-588)4043793-0 \|2 gnd \|9 rswk-swf
650	0	7	\|a Reaktionsmechanismus \|0 (DE-588)4177123-0 \|2 gnd \|9 rswk-swf
650	0	7	\|a Namensreaktion \|0 (DE-588)4171139-7 \|2 gnd \|9 rswk-swf
655		7	\|8 1\p \|0 (DE-588)4066724-8 \|a Wörterbuch \|2 gnd-content
689	0	0	\|a Namensreaktion \|0 (DE-588)4171139-7 \|D s
689	0	1	\|a Reaktionsmechanismus \|0 (DE-588)4177123-0 \|D s
689	0		\|5 DE-604
689	1	0	\|a Organische Chemie \|0 (DE-588)4043793-0 \|D s
689	1	1	\|a Namensreaktion \|0 (DE-588)4171139-7 \|D s
689	1	2	\|a Reaktionsmechanismus \|0 (DE-588)4177123-0 \|D s
689	1		\|8 2\p \|5 DE-604
856	4	2	\|m SWB Datenaustausch \|q application/pdf \|u http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=010402802&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA \|3 Inhaltsverzeichnis
999			\|a oai:aleph.bib-bvb.de:BVB01-010402802
883	1		\|8 1\p \|a cgwrk \|d 20201028 \|q DE-101 \|u https://d-nb.info/provenance/plan#cgwrk
883	1		\|8 2\p \|a cgwrk \|d 20201028 \|q DE-101 \|u https://d-nb.info/provenance/plan#cgwrk

Record in the Search Index

_version_	1804130109293068288
adam_text	IX TABLE OF CONTENTS ABBREVIATIONS ....................................................................................................XVII 1. ABNORMAL CLAISEN REARRANGEMENT..............................................................1 2. ALDER ENE REACTION .....................................................................................2 3. ALDOL CONDENSATION....................................................................................3 4. ALLANROBINSON REACTION...........................................................................4 5. ALPER CARBONYLATION...................................................................................6 6. AMADORI REARRANGEMENT ............................................................................8 7. ANGELIRIMINI HYDROXAMIC ACID SYNTHESIS................................................9 8. ANRORC MECHANISM.............................................................................10 9. ARNDTEISTERT HOMOLOGATION....................................................................11 10. AUWERS REACTION ......................................................................................13 11. BAEYERDREWSON INDIGO SYNTHESIS ..........................................................14 12. BAEYERVILLIGER OXIDATION.......................................................................16 13. BAKERVENKATARAMAN REARRANGEMENT ......................................................17 14. BAMBERGER REARRANGEMENT.......................................................................18 15. BAMFORDSTEVENS REACTION ......................................................................19 16. BARGELLINI REACTION...................................................................................20 17. BARTOLI INDOLE SYNTHESIS ...........................................................................21 18. BARTON DECARBOXYLATION ...........................................................................23 19. BARTONMCCOMBIE DEOXYGENATION .........................................................24 20. BARTON NITRITE PHOTOLYSIS..........................................................................25 21. BAYLISHILLMAN REACTION..........................................................................26 22. BECKMANN REARRANGEMENT........................................................................28 23. BEIRUT REACTION.........................................................................................29 24. BENZILIC ACID REARRANGEMENT....................................................................31 25. BENZOIN CONDENSATION .............................................................................32 26. BERGMAN CYCLIZATION................................................................................33 27. BIGINELLI PYRIMIDONE SYNTHESIS................................................................34 28. BIRCH REDUCTION........................................................................................36 29. BISCHLERMOEHLAU INDOLE SYNTHESIS ..........................................................38 30. BISCHLERNAPIERALSKI REACTION .................................................................39 31. BLAISE REACTION.........................................................................................40 32. BLANC CHLOROMETHYLATION REACTION ...........................................................41 33. BOEKELHEIDE REACTION...............................................................................42 34. BOGER PYRIDINE SYNTHESIS .........................................................................43 35. BOORD REACTION.........................................................................................44 36. BORSCHEDRECHSEL CYCLIZATION .................................................................45 37. BOULTONKATRITZKY REARRANGEMENT...........................................................46 38. BOUVEAULT ALDEHYDE SYNTHESIS .................................................................47 39. BOUVEAULTBLANC REDUCTION.....................................................................48 40. BOYLANDSIMS OXIDATION .........................................................................49 41. BRADSHER REACTION ....................................................................................51 42. BROOK REARRANGEMENT...............................................................................52 X 43. BROWN HYDROBORATION REACTION ................................................................53 44. BUCHERER CARBAZOLE SYNTHESIS ..................................................................54 45. BUCHERER REACTION ....................................................................................56 46. BUCHERERBERGS REACTION.........................................................................57 47. BUCHNERCURTIUSSCHLOTTERBECK REACTION................................................58 48. BUCHNER METHOD OF RING EXPANSION .........................................................59 49. BUCHWALDHARTWIG CN BOND AND CO BOND FORMATION REACTIONS........60 50. BURGESS DEHYDRATING REAGENT ...................................................................61 51. CADIOTCHODKIEWICZ COUPLING ................................................................62 52. CANNIZZARO DISPROPOTIONATION REACTION....................................................63 53. CARROLL REARRANGEMENT .............................................................................65 54. CASTROSTEPHENS COUPLING.......................................................................66 55. CHAPMAN REARRANGEMENT .........................................................................67 56. CHICHIBABIN AMINATION REACTION ..............................................................68 57. CHICHIBABIN PYRIDINE SYNTHESIS ...............................................................69 58. CHUGAEV REACTION.....................................................................................71 59. CIAMICIANDENNSTED REARRANGEMENT .......................................................72 60. CLAISEN CONDENSATION...............................................................................73 61. CLAISEN REARRANGEMENT.............................................................................74 62. CLARKEESCHWEILER REDUCTIVE ALKYLATION OF AMINES .................................76 63. CLEMMENSEN REDUCTION............................................................................77 64. COMBES QUINOLINE SYNTHESIS....................................................................79 65. CONRADLIMPACH REACTION.......................................................................81 66. COOKHEILBRON THIAZOLE SYNTHESIS...........................................................82 67. COPE ELIMINATION REACTION .......................................................................83 68. COPE, OXY-COPE, AND ANIONIC OXY-COPE REARRANGEMENTS........................84 69. COREYBAKSHISHIBATA (CBS) REDUCTION.................................................86 70. COREY CHAYKOVSKY REACTION...................................................................88 71. COREYFUCHS REACTION .............................................................................90 72. COREYKIM OXIDATION..............................................................................92 73. COREYWINTER OLEFIN SYNTHESIS................................................................93 74. CORNFORTH REARRANGEMENT.........................................................................95 75. CRIEGEE GLYCOL CLEAVAGE ..........................................................................96 76. CRIEGEE MECHANISM OF OZONOLYSIS...........................................................97 77. CURTIUS REARRANGEMENT.............................................................................98 78. DAKIN OXIDATION.......................................................................................99 79. DAKINWEST REACTION.............................................................................100 80. DANHEISER ANNULATION.............................................................................102 81. DARZENS GLYCIDIC ESTER CONDENSATION .....................................................103 82. DAVIS CHIRAL OXAZIRIDINE REAGENT............................................................104 83. DE MAYO REACTION...................................................................................105 84. DEMJANOV REARRANGEMENT......................................................................107 85. DESSMARTIN PERIODINANE OXIDATION ......................................................109 86. DIECKMANN CONDENSATION ......................................................................110 87. DIELSALDER REACTION .............................................................................111 88. DIENONEPHENOL REARRANGEMENT ............................................................113 XI 89. DI- -METHANE REARRANGEMENT ................................................................114 90. DOEBNER REACTION ...................................................................................115 91. DOEBNERVON MILLER REACTION ................................................................117 92. DOERINGLAFLAMME ALLENE SYNTHESIS ....................................................119 93. DORNOWWIEHLER ISOXAZOLE SYNTHESIS ...................................................120 94. DOETZ REACTION.........................................................................................122 95. DOWD RING EXPANSION ............................................................................123 96. DUTTWORMALL REACTION..........................................................................125 97. EGLINTON REACTION ...................................................................................126 98. ESCHENMOSER COUPLING REACTION.............................................................127 99. ESCHENMOSERTANABE FRAGMENTATION ....................................................128 100. ETARD REACTION ........................................................................................129 101. EVANS ALDOL REACTION ..............................................................................130 102. FAVORSKII REARRANGEMENT AND QUASI-FAVORSKII REARRANGEMENT ..............132 103. FEISTBENARY FURAN SYNTHESIS ................................................................134 104. FERRIER REARRANGEMENT............................................................................135 105. FINKELSTEIN REACTION ...............................................................................136 106. FISCHERHEPP REARRANGEMENT ................................................................137 107. FISCHER INDOLE SYNTHESIS ........................................................................138 108. FISCHERSPEIER ESTERIFICATION.................................................................139 109. FLEMING OXIDATION .................................................................................140 110. FORSTER REACTION .....................................................................................142 111. FRATERSEEBACH ALKYLATION.....................................................................144 112. FRIEDELCRAFTS REACTION..........................................................................145 113. FRIEDLAENDER SYNTHESIS.............................................................................147 114. FRIES REARRANGEMENT...............................................................................149 115. FRITSCHBUTTENBERGWIECHELL REARRANGEMENT........................................151 116. FUJIMOTOBELLEAU REACTION ....................................................................152 117. FUKUYAMA AMINE SYNTHESIS ...................................................................153 118. GABRIEL SYNTHESIS ...................................................................................155 119. GASSMAN INDOLE SYNTHESIS .....................................................................156 120. GATTERMANNKOCH REACTION ...................................................................157 121. GEWALD AMINOTHIOPHENE SYNTHESIS ........................................................158 122. GLASER COUPLING .....................................................................................160 123. GOMBERGBACHMANN REACTION...............................................................161 124. GRIBBLE INDOLE REDUCTION .......................................................................162 125. GRIBBLE REDUCTION OF DIARYL KETONES.......................................................163 126. GRIGNARD REACTION ..................................................................................164 127. GROB FRAGMENTATION ...............................................................................166 128. GUARESCHITHORPE CONDENSATION ...........................................................168 129. HAJOSWIECHERT REACTION.......................................................................169 130. HALLERBAUER REACTION ...........................................................................171 131. HANTZSCH PYRIDINE SYNTHESIS..................................................................172 132. HANTZSCH PYRROLE SYNTHESIS....................................................................174 133. HAWORTH REACTION...................................................................................175 134. HAYASHI REARRANGEMENT..........................................................................177 XII 135. HECK REACTION ........................................................................................179 136. HEGEDUS INDOLE SYNTHESIS ......................................................................181 137. HELLVOLHARDTZELINSKY REACTION..........................................................182 138. HENRY REACTION (NITROALDOL REACTION)......................................................183 139. HERZ REACTION.........................................................................................184 140. HETEROARYL HECK REACTION ......................................................................186 141. HIYAMA CROSS-COUPLING REACTION............................................................187 142. HOCHCAMPBELL AZIRIDINE SYNTHESIS......................................................189 143. HODGESVEDEJS METALLATION OF OXAZOLES ...............................................191 144. HOFMANN REARRANGEMENT (HOFMANN DEGRADATION REACTION) ...................192 145. HOFMANNLOEFFLERFREYTAG REACTION ......................................................193 146. HOFMANNMARTIUS REACTION (REILLYHICKINBOTTOM REARRANGEMENT) .....194 147. HOOKER OXIDATION ..................................................................................196 148. HORNERWADSWORTHEMMONS REACTION.................................................198 149. HOUBENHOESCH SYNTHESIS ....................................................................200 150. HUNSDIECKER REACTION.............................................................................202 151. INGMANSKE PROCEDURE..........................................................................203 152. JACOBSENKATSUKI EPOXIDATION ..............................................................204 153. JACOBSEN REARRANGEMENT ........................................................................206 154. JAPPKLINGEMANN HYDRAZONE SYNTHESIS ................................................208 155. JULIALYTHGOE OLEFINATION .....................................................................209 156. KAHNE GLYCOSIDATION..............................................................................211 157. KECK STEREOSELECTIVE ALLYLATION..............................................................213 158. KECK MACROLACTONIZATION.......................................................................215 159. KEMP ELIMINATION..................................................................................217 160. KENNEDY OXIDATIVE CYCLIZATION..............................................................218 161. KHARASCH ADDITION REACTION....................................................................219 162. KNOEEVENAGEL CONDENSATION....................................................................220 163. KNORR PYRROLE SYNTHESIS.........................................................................222 164. KOCH CARBONYLATION REACTION (KOCHHAAF CARBONYLATION REACTION)......223 165. KOENIGKNORR GLYCOSIDATION.................................................................225 166. KOLBE ELECTROLYTIC COUPLING...................................................................226 167. KOLBESCHMITT REACTION.........................................................................227 168. KOSTANECKI REACTION...............................................................................228 169. KRAPCHO DECARBOXYLATION ......................................................................230 170. KROEHNKE REACTION (PYRIDINE SYNTHESIS) ..................................................231 171. KUMADA CROSS-COUPLING REACTION...........................................................233 172. LAROCK INDOLE SYNTHESIS.........................................................................235 173. LAWESSONS REAGENT...............................................................................236 174. LEUCKARTWALLACH REACTION ...................................................................237 175. LIEBEN HALOFORM REACTION ......................................................................238 176. LIEBESKINDSROGL COUPLING ...................................................................239 177. LOSSEN REARRANGEMENT ...........................................................................240 178. LUCHE REDUCTION ....................................................................................241 179. MCFADYENSTEVENS REDUCTION ...............................................................242 180. MCLAFFERTY REARRANGEMENT ....................................................................243 XIII 181. MCMURRY COUPLING ................................................................................244 182. MADELUNG INDOLE SYNTHESIS....................................................................245 183. MANNICH REACTION...................................................................................246 184. MARSHALL BORONATE FRAGMENTATION ..........................................................248 185. MARTINS SULFURANE DEHYDRATING REAGENT ................................................249 186. MASAMUNEROUSH CONDITIONS ...............................................................251 187. MEERWEIN ARYLATION ...............................................................................253 188. MEERWEINPONNDORFVERLEY REDUCTION.................................................254 189. MEINWALD REARRANGEMENT ......................................................................255 190. MEISENHEIMER COMPLEX .........................................................................256 191. MEISENHEIMER REARRANGEMENT................................................................258 192. MEYERSCHUSTER REARRANGEMENT.............................................................259 193. MICHAEL ADDITION ...................................................................................260 194. MICHAELISARBUZOV PHOSPHONATE SYNTHESIS ..........................................261 195. MIDLAND REDUCTION .................................................................................262 196. MILLERLOUDONSNYDER NITRILE SYNTHESIS ...............................................263 197. MISLOWEVANS REARRANGEMENT...............................................................264 198. MITSUNOBU REACTION................................................................................265 199. MIYAURA BORATION REACTION .....................................................................266 200. MOFFATT OXIDATION ..................................................................................267 201. MORGANWALLS REACTION (PICTETHUBERT REACTION) .................................269 202. MORIBAN INDOLE SYNTHESIS....................................................................270 203. MORIN REARRANGEMENT.............................................................................272 204. MUKAIYAMA ALDOL REACTION.....................................................................274 205. MUKAIYAMA ESTERIFICATION......................................................................275 206. MYERS * SAITO CYCLIZATION........................................................................277 207. NAMETKIN REARRANGEMENT (RETROPINACOL REARRANGEMENT) ........................279 208. NAZAROV CYCLIZATION...............................................................................280 209. NEBER REARRANGEMENT.............................................................................281 210. NEF REACTION...........................................................................................282 211. NEGISHI CROSS-COUPLING REACTION ............................................................283 212. NENITZESCU INDOLE SYNTHESIS ..................................................................284 213. NICHOLAS REACTION...................................................................................286 214. NOYORI ASYMMETRIC HYDROGENATION........................................................287 215. NOZAKIHIYAMAKISHI REACTION ............................................................289 216. OPPENAUER OXIDATION .............................................................................290 217. ORTON REARRANGEMENT .............................................................................292 218. OVERMAN REARRANGEMENT........................................................................293 219. PAALKNORR FURAN SYNTHESIS ...................................................................294 220. PAALKNORR PYRROLE SYNTHESIS ................................................................295 221. PARHAM CYCLIZATION................................................................................296 222. PASSERINI REACTION ..................................................................................298 223. PATERNOBUECHI REACTION .........................................................................299 224. PAUSONKHAND CYCLOPENTENONE SYNTHESIS .............................................300 225. PAYNE REARRANGEMENT.............................................................................302 226. PECHMANN CONDENSATION (COUMARIN SYNTHESIS)......................................303 XIV 227. PECHMANN PYRAZOLE SYNTHESIS................................................................304 228. PERKIN REACTION (CINNAMIC ACID SYNTHESIS).............................................305 229. PERKOW VINYL PHOSPHATE SYNTHESIS ........................................................307 230. PETERSON OLEFINATION...............................................................................308 231. PFAUPLATTNER AZULENE SYNTHESIS ............................................................310 232. PFITZINGER QUINOLINE SYNTHESIS ...............................................................311 233. PICTETGAMS ISOQUINOLINE SYNTHESIS......................................................312 234. PICTETSPENGLER TETRAHYDROISOQUINOLINE SYNTHESIS.................................314 235. PINACOL REARRANGEMENT...........................................................................315 236. PINNER SYNTHESIS ....................................................................................316 237. POLONOVSKI REACTION...............................................................................317 238. POLONOVSKIPOTIER REARRANGEMENT .........................................................319 239. POMERANZFRITSCH REACTION....................................................................320 240. PREVOST TRANS -DIHYDROXYLATION...............................................................322 241. PRILEZHAEV REACTION................................................................................323 242. PRINS REACTION ........................................................................................324 243. PSCHORR RING CLOSURE ..............................................................................325 244. PUMMERER REARRANGEMENT......................................................................327 245. RAMBERGBAECKLUND OLEFIN SYNTHESIS.....................................................328 246. REFORMATSKY REACTION ............................................................................329 247. REGITZ DIAZO SYNTHESIS...........................................................................330 248. REIMERTIEMANN REACTION.....................................................................332 249. REISSERT REACTION (ALDEHYDE SYNTHESIS) ..................................................334 250. RILEY OXIDATION (SELENIUM DIOXIDE OXIDATION).......................................336 251. RING-CLOSING METATHESIS (RCM) USING GRUBBS AND SCHROCK CATALYSTS ..337 252. RITTER REACTION........................................................................................339 253. ROBINSON ANNULATION .............................................................................340 254. ROBINSONSCHOEPF REACTION ....................................................................341 255. ROSENMUND REDUCTION ...........................................................................343 256. ROUSH ALLYLBORONATE REAGENT..................................................................344 257. RUBOTTOM OXIDATION...............................................................................345 258. RUPE REARRANGEMENT ..............................................................................346 259. RYCHNOVSKY POLYOL SYNTHESIS................................................................347 260. SAKURAI ALLYLATION REACTION (HOSOMISAKURAI REACTION) ........................349 261. SANDMEYER REACTION...............................................................................350 262. SARETT OXIDATION ....................................................................................351 263. SCHIEMANN REACTION (BALZ SCHIEMANN REACTION) ..................................354 264. SCHLOSSER MODIFICATION OF THE WITTIG REACTION.......................................355 265. SCHMIDT REACTION ...................................................................................356 266. SCHMIDTS TRICHLOROACETIMIDATE GLYCOSIDATION REACTION .........................357 267. SCHOLL REACTION ......................................................................................359 268. SCHOEPF REACTION .....................................................................................361 269. SCHOTTENBAUMANN REACTION..................................................................362 270. SHAPIRO REACTION ....................................................................................363 271. SHARPLESS ASYMMETRIC AMINO HYDROXYLATION .........................................364 272. SHARPLESS ASYMMETRIC EPOXIDATION .......................................................366 XV 273. SHARPLESS DIHYDROXYLATION.....................................................................369 274. SHI ASYMMETRIC EPOXIDATION..................................................................372 275. SIMMONSSMITH REACTION .....................................................................374 276. SIMONINI REACTION ..................................................................................375 277. SIMONIS CHROMONE CYCLIZATION ..............................................................376 278. SKRAUP QUINOLINE SYNTHESIS....................................................................378 279. SMILES REARRANGEMENT............................................................................380 280. SOMMELET REACTION.................................................................................381 281. SOMMELETHAUSER (AMMONIUM YLIDE) REARRANGEMENT...........................383 282. SONOGASHIRA REACTION .............................................................................384 283. STAUDINGER REACTION................................................................................386 284. STETTER REACTION (MICHAEL * STETTER REACTION) ...........................................387 285. STEVENS REARRANGEMENT ..........................................................................389 286. STIEGLITZ REARRANGEMENT .........................................................................390 287. STILLGENNARI PHOSPHONATE REACTION ......................................................392 288. STILLE COUPLING .......................................................................................393 289. STILLEKELLY REACTION..............................................................................394 290. STOBBE CONDENSATION..............................................................................396 291. STOLLE SYNTHESIS......................................................................................397 292. STORK ENAMINE REACTION..........................................................................398 293. STRECKER AMINO ACID SYNTHESIS ...............................................................399 294. SUZUKI COUPLING.....................................................................................400 295. SWERN OXIDATION ....................................................................................402 296. TAMAOKUMADA OXIDATION ....................................................................404 297. TEBBE OLEFINATION (PETASIS ALKENYLATION) ...............................................405 298. THORPEZIEGLER REACTION........................................................................407 299. TIEMANN REARRANGEMENT ........................................................................408 300. TIFFENEAUDEMJANOV REARRANGEMENT.....................................................409 301. TISHCHENKO REACTION ..............................................................................411 302. TOLLENS REACTION.....................................................................................412 303. TSUJITROST ALLYLATION............................................................................414 304. UENOSTORK CYCLIZATION.........................................................................415 305. UGI REACTION...........................................................................................416 306. ULLMANN REACTION...................................................................................418 307. VILSMEIERHAACK REACTION.....................................................................419 308. VON BRAUN REACTION ................................................................................421 309. VON RICHTER REACTION ..............................................................................422 310. WACKER OXIDATION ..................................................................................424 311. WAGNERMEERWEIN REARRANGEMENT........................................................426 312. WALLACH REARRANGEMENT .........................................................................427 313. WEINREB AMIDE ......................................................................................428 314. WEISS REACTION .......................................................................................429 315. WENKER AZIRIDINE SYNTHESIS ...................................................................431 316. WHARTON OXYGEN TRANSPOSITION REACTION.................................................432 317. WILLGERODTKINDLER REACTION .................................................................433 318. WILLIAMSON ETHER SYNTHESIS ...................................................................437 XVI 319. WITTIG REACTION ......................................................................................438 320. [1,2]-WITTIG REARRANGEMENT ...................................................................439 321. [2,3]-WITTIG REARRANGEMENT ...................................................................440 322. WOHLZIEGLER REACTION ..........................................................................441 323. WOLFF REARRANGEMENT .............................................................................443 324. WOLFFKISHNER REDUCTION ......................................................................444 325. WOODWARD CIS -DIHYDROXYLATION.............................................................445 326. WURTZ REACTION.......................................................................................446 327. YAMADA COUPLING REAGENT......................................................................447 328. YAMAGUCHI ESTERIFICATION ......................................................................448 329. ZAITSEV ELIMINATION................................................................................450 330. ZINCKE REACTION......................................................................................451 331. ZININ BENZIDINE REARRANGEMENT (SEMIDINE REARRANGEMENT)....................453 SUBJECT INDEX.......................................................................................................455
any_adam_object	1
author	Li, Jie Jack 1964-
author_GND	(DE-588)123481848
author_facet	Li, Jie Jack 1964-
author_role	aut
author_sort	Li, Jie Jack 1964-
author_variant	j j l jj jjl
building	Verbundindex
bvnumber	BV017258850
callnumber-first	Q - Science
callnumber-label	QD291
callnumber-raw	QD291
callnumber-search	QD291
callnumber-sort	QD 3291
callnumber-subject	QD - Chemistry
classification_rvk	VK 5503 VK 6003
ctrlnum	(OCoLC)52911268 (DE-599)BVBBV017258850
dewey-full	547.2
dewey-hundreds	500 - Natural sciences and mathematics
dewey-ones	547 - Organic chemistry
dewey-raw	547.2
dewey-search	547.2
dewey-sort	3547.2
dewey-tens	540 - Chemistry and allied sciences
discipline	Chemie / Pharmazie
edition	2. ed.
format	Book
fullrecord	<?xml version="1.0" encoding="UTF-8"?><collection xmlns="http://www.loc.gov/MARC21/slim"><record><leader>02403nam a2200625 c 4500</leader><controlfield tag="001">BV017258850</controlfield><controlfield tag="003">DE-604</controlfield><controlfield tag="005">20041026 </controlfield><controlfield tag="007">t</controlfield><controlfield tag="008">030624s2003 gw \|\|\|\| 00\|\|\| eng d</controlfield><datafield tag="016" ind1="7" ind2=" "><subfield code="a">967883784</subfield><subfield code="2">DE-101</subfield></datafield><datafield tag="020" ind1=" " ind2=" "><subfield code="a">3540402039</subfield><subfield code="9">3-540-40203-9</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(OCoLC)52911268</subfield></datafield><datafield tag="035" ind1=" " ind2=" "><subfield code="a">(DE-599)BVBBV017258850</subfield></datafield><datafield tag="040" ind1=" " ind2=" "><subfield code="a">DE-604</subfield><subfield code="b">ger</subfield><subfield code="e">rakddb</subfield></datafield><datafield tag="041" ind1="0" ind2=" "><subfield code="a">eng</subfield></datafield><datafield tag="044" ind1=" " ind2=" "><subfield code="a">gw</subfield><subfield code="c">DE</subfield></datafield><datafield tag="049" ind1=" " ind2=" "><subfield code="a">DE-29T</subfield><subfield code="a">DE-19</subfield><subfield code="a">DE-703</subfield><subfield code="a">DE-11</subfield></datafield><datafield tag="050" ind1=" " ind2="0"><subfield code="a">QD291</subfield></datafield><datafield tag="082" ind1="0" ind2=" "><subfield code="a">547.2</subfield><subfield code="2">21</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">VK 5503</subfield><subfield code="0">(DE-625)147401:256</subfield><subfield code="2">rvk</subfield></datafield><datafield tag="084" ind1=" " ind2=" "><subfield code="a">VK 6003</subfield><subfield code="0">(DE-625)147413:256</subfield><subfield code="2">rvk</subfield></datafield><datafield tag="100" ind1="1" ind2=" "><subfield code="a">Li, Jie Jack</subfield><subfield code="d">1964-</subfield><subfield code="e">Verfasser</subfield><subfield code="0">(DE-588)123481848</subfield><subfield code="4">aut</subfield></datafield><datafield tag="245" ind1="1" ind2="0"><subfield code="a">Name reactions</subfield><subfield code="b">a collection of detailed reaction mechanisms</subfield><subfield code="c">Jie Jack Li</subfield></datafield><datafield tag="250" ind1=" " ind2=" "><subfield code="a">2. ed.</subfield></datafield><datafield tag="264" ind1=" " ind2="1"><subfield code="a">Berlin [u.a.]</subfield><subfield code="b">Springer</subfield><subfield code="c">2003</subfield></datafield><datafield tag="300" ind1=" " ind2=" "><subfield code="a">XVIII, 465 S.</subfield></datafield><datafield tag="336" ind1=" " ind2=" "><subfield code="b">txt</subfield><subfield code="2">rdacontent</subfield></datafield><datafield tag="337" ind1=" " ind2=" "><subfield code="b">n</subfield><subfield code="2">rdamedia</subfield></datafield><datafield tag="338" ind1=" " ind2=" "><subfield code="b">nc</subfield><subfield code="2">rdacarrier</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Chemische reacties</subfield><subfield code="2">gtt</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chimie organique</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Naamgeving</subfield><subfield code="2">gtt</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Organische chemie</subfield><subfield code="2">gtt</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Organische verbindingen</subfield><subfield code="2">gtt</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Reactiemechanismen (chemie)</subfield><subfield code="2">gtt</subfield></datafield><datafield tag="650" ind1=" " ind2="7"><subfield code="a">Reações químicas</subfield><subfield code="2">larpcal</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Réactions organiques (Chimie)</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chemical reactions</subfield></datafield><datafield tag="650" ind1=" " ind2="4"><subfield code="a">Chemistry, Organic</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Organische Chemie</subfield><subfield code="0">(DE-588)4043793-0</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Reaktionsmechanismus</subfield><subfield code="0">(DE-588)4177123-0</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="650" ind1="0" ind2="7"><subfield code="a">Namensreaktion</subfield><subfield code="0">(DE-588)4171139-7</subfield><subfield code="2">gnd</subfield><subfield code="9">rswk-swf</subfield></datafield><datafield tag="655" ind1=" " ind2="7"><subfield code="8">1\p</subfield><subfield code="0">(DE-588)4066724-8</subfield><subfield code="a">Wörterbuch</subfield><subfield code="2">gnd-content</subfield></datafield><datafield tag="689" ind1="0" ind2="0"><subfield code="a">Namensreaktion</subfield><subfield code="0">(DE-588)4171139-7</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2="1"><subfield code="a">Reaktionsmechanismus</subfield><subfield code="0">(DE-588)4177123-0</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="0" ind2=" "><subfield code="5">DE-604</subfield></datafield><datafield tag="689" ind1="1" ind2="0"><subfield code="a">Organische Chemie</subfield><subfield code="0">(DE-588)4043793-0</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="1" ind2="1"><subfield code="a">Namensreaktion</subfield><subfield code="0">(DE-588)4171139-7</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="1" ind2="2"><subfield code="a">Reaktionsmechanismus</subfield><subfield code="0">(DE-588)4177123-0</subfield><subfield code="D">s</subfield></datafield><datafield tag="689" ind1="1" ind2=" "><subfield code="8">2\p</subfield><subfield code="5">DE-604</subfield></datafield><datafield tag="856" ind1="4" ind2="2"><subfield code="m">SWB Datenaustausch</subfield><subfield code="q">application/pdf</subfield><subfield code="u">http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=010402802&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA</subfield><subfield code="3">Inhaltsverzeichnis</subfield></datafield><datafield tag="999" ind1=" " ind2=" "><subfield code="a">oai:aleph.bib-bvb.de:BVB01-010402802</subfield></datafield><datafield tag="883" ind1="1" ind2=" "><subfield code="8">1\p</subfield><subfield code="a">cgwrk</subfield><subfield code="d">20201028</subfield><subfield code="q">DE-101</subfield><subfield code="u">https://d-nb.info/provenance/plan#cgwrk</subfield></datafield><datafield tag="883" ind1="1" ind2=" "><subfield code="8">2\p</subfield><subfield code="a">cgwrk</subfield><subfield code="d">20201028</subfield><subfield code="q">DE-101</subfield><subfield code="u">https://d-nb.info/provenance/plan#cgwrk</subfield></datafield></record></collection>
genre	1\p (DE-588)4066724-8 Wörterbuch gnd-content
genre_facet	Wörterbuch
id	DE-604.BV017258850
illustrated	Not Illustrated
indexdate	2024-07-09T19:15:48Z
institution	BVB
isbn	3540402039
language	English
oai_aleph_id	oai:aleph.bib-bvb.de:BVB01-010402802
oclc_num	52911268
open_access_boolean
owner	DE-29T DE-19 DE-BY-UBM DE-703 DE-11
owner_facet	DE-29T DE-19 DE-BY-UBM DE-703 DE-11
physical	XVIII, 465 S.
publishDate	2003
publishDateSearch	2003
publishDateSort	2003
publisher	Springer
record_format	marc
spelling	Li, Jie Jack 1964- Verfasser (DE-588)123481848 aut Name reactions a collection of detailed reaction mechanisms Jie Jack Li 2. ed. Berlin [u.a.] Springer 2003 XVIII, 465 S. txt rdacontent n rdamedia nc rdacarrier Chemische reacties gtt Chimie organique Naamgeving gtt Organische chemie gtt Organische verbindingen gtt Reactiemechanismen (chemie) gtt Reações químicas larpcal Réactions organiques (Chimie) Chemical reactions Chemistry, Organic Organische Chemie (DE-588)4043793-0 gnd rswk-swf Reaktionsmechanismus (DE-588)4177123-0 gnd rswk-swf Namensreaktion (DE-588)4171139-7 gnd rswk-swf 1\p (DE-588)4066724-8 Wörterbuch gnd-content Namensreaktion (DE-588)4171139-7 s Reaktionsmechanismus (DE-588)4177123-0 s DE-604 Organische Chemie (DE-588)4043793-0 s 2\p DE-604 SWB Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=010402802&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA Inhaltsverzeichnis 1\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk 2\p cgwrk 20201028 DE-101 https://d-nb.info/provenance/plan#cgwrk
spellingShingle	Li, Jie Jack 1964- Name reactions a collection of detailed reaction mechanisms Chemische reacties gtt Chimie organique Naamgeving gtt Organische chemie gtt Organische verbindingen gtt Reactiemechanismen (chemie) gtt Reações químicas larpcal Réactions organiques (Chimie) Chemical reactions Chemistry, Organic Organische Chemie (DE-588)4043793-0 gnd Reaktionsmechanismus (DE-588)4177123-0 gnd Namensreaktion (DE-588)4171139-7 gnd
subject_GND	(DE-588)4043793-0 (DE-588)4177123-0 (DE-588)4171139-7 (DE-588)4066724-8
title	Name reactions a collection of detailed reaction mechanisms
title_auth	Name reactions a collection of detailed reaction mechanisms
title_exact_search	Name reactions a collection of detailed reaction mechanisms
title_full	Name reactions a collection of detailed reaction mechanisms Jie Jack Li
title_fullStr	Name reactions a collection of detailed reaction mechanisms Jie Jack Li
title_full_unstemmed	Name reactions a collection of detailed reaction mechanisms Jie Jack Li
title_short	Name reactions
title_sort	name reactions a collection of detailed reaction mechanisms
title_sub	a collection of detailed reaction mechanisms
topic	Chemische reacties gtt Chimie organique Naamgeving gtt Organische chemie gtt Organische verbindingen gtt Reactiemechanismen (chemie) gtt Reações químicas larpcal Réactions organiques (Chimie) Chemical reactions Chemistry, Organic Organische Chemie (DE-588)4043793-0 gnd Reaktionsmechanismus (DE-588)4177123-0 gnd Namensreaktion (DE-588)4171139-7 gnd
topic_facet	Chemische reacties Chimie organique Naamgeving Organische chemie Organische verbindingen Reactiemechanismen (chemie) Reações químicas Réactions organiques (Chimie) Chemical reactions Chemistry, Organic Organische Chemie Reaktionsmechanismus Namensreaktion Wörterbuch
url	http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=010402802&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA
work_keys_str_mv	AT lijiejack namereactionsacollectionofdetailedreactionmechanisms

Holdings

There is no print copy available.

Interlibrary loan Place Request Caution: Not in THWS collection! Indexes

MARC

Record in the Search Index

There is no print copy available.

Similar Items