Verfügbarkeit: Name reactions

Name reactions: a collection of detailed reaction mechanisms and synthetic applications

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Bibliographische Detailangaben
1. Verfasser:	Li, Jie Jack 1964- (VerfasserIn)
Format:	Buch
Sprache:	English
Veröffentlicht:	Berlin [u.a.] Springer 2009
Ausgabe:	4., expanded ed.
Schlagworte:	Chemical reactions Chemistry, Organic Organische Chemie Reaktionsmechanismus Namensreaktion Wörterbuch
Online-Zugang:	Inhaltsverzeichnis
Beschreibung:	XXII, 621 S. Ill., graph. Darst.
ISBN:	9783642010521 3540300309

Internformat

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Datensatz im Suchindex

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adam_text	Titel: Name reactions Autor: Li, Jie Jack Jahr: 2009 Table of Contents Foreword............................................................................................................... VII Preface.................................................................................................................. IX Abbreviations.......................................................................................................XIX Alder ene reaction.....................................................................................................1 Aldol condensation....................................................................................................3 Algar-Flynn-Oyamada reaction...............................................................................6 Allan-Robinson reaction...........................................................................................8 Arndt-Eistert homologation....................................................................................10 Baeyer-Villiger oxidation.......................................................................................12 Baker-Venkataraman rearrangement......................................................................14 Bamford-Stevens reaction......................................................................................16 Barbier coupling reaction........................................................................................18 Bartoli indole synthesis...........................................................................................20 Barton radical decarboxylation...............................................................................22 Barton-McCombie deoxygenation.........................................................................24 Barton nitrite photolysis..........................................................................................26 Batcho-Leimgruber indole synthesis......................................................................28 Baylis-Hillman reaction..........................................................................................30 Beckmann rearrangement........................................................................................33 Abnormal Beckmann rearrangement............................................................34 Benzilic acid rearrangement....................................................................................36 Benzoin condensation..............................................................................................38 Bergman cyclization................................................................................................40 Biginelli pyrimidone synthesis................................................................................42 Birch reduction........................................................................................................44 Bischler-Möhlau indole synthesis..........................................................................46 Bischler-Napieralski reaction.................................................................................48 Blaise reaction ........................................................................................................50 Blum-Ittah aziridine synthesis...............................................................................52 Boekelheide reaction...............................................................................................54 Boger pyridine synthesis.........................................................................................56 Borch reductive amination......................................................................................58 Borsche-Drechsel cyclization.................................................................................60 Boulton-Katritzky rearrangement...........................................................................62 Bouveault, aldehyde synthesis.................................................................................64 Bouveault-Blanc reduction.....................................................................................65 Bradsher reaction.....................................................................................................66 Brook rearrangement...............................................................................................68 Brown hydroboration..............................................................................................70 Bucherer carbazole synthesis..................................................................................72 XII Bucherer reaction.....................................................................................................74 Bucherer-Bergs reaction.........................................................................................76 Büchner ring expansion...........................................................................................78 Buchwald-Hartwig amination................................................................................80 Burgess dehydrating reagent...................................................................................84 Burke boronates.......................................................................................................87 Cadiot-Chodkiewicz coupling................................................................................90 Camps quinoline synthesis......................................................................................92 Cannizzaro reaction.................................................................................................94 Carroll rearrangement.............................................................................................96 Castro-Stephens coupling.......................................................................................98 Chan alkyne reduction...........................................................................................100 Chan-Lam C-X coupling reaction.......................................................................102 Chapman rearrangement.......................................................................................105 Chichibabin pyridine synthesis.............................................................................107 Chugaev reaction...................................................................................................110 Ciamician-Dennsted rearrangement.....................................................................112 Claisen condensation.............................................................................................113 Claisen isoxazole synthesis...................................................................................115 Claisen rearrangement...........................................................................................117 para-Claisen rearrangement.......................................................................119 Abnormal Claisen rearrangement................................................................121 Eschenmoser-Claisen amide acetal rearrangement....................................123 Ireland-Claisen (silyl ketene acetal) rearrangement...................................125 Johnson-Claisen (orthoester) rearrangement..............................................127 Clemmensen reduction..........................................................................................129 Combes quinoline synthesis..................................................................................131 Conrad-Limpach reaction.....................................................................................133 Cope elimination reaction.....................................................................................135 Cope rearrangement..............................................................................................137 Anionic oxy-Cope rearrangement.................................................................138 Oxy-Cope rearrangement..............................................................................140 Siloxy-Cope rearrangement..........................................................................141 Corey-Bakshi-Shibata (CBS) reagent.................................................................143 Corey-Chaykovsky reaction.................................................................................146 Corey-Fuchs reaction............................................................................................148 Corey-Kim oxidation............................................................................................150 Corey-Nicolaoumacrolactonization....................................................................152 Corey-Seebach reaction........................................................................................154 Corey-Winter olefin synthesis..............................................................................156 Criegee glycol cleavage........................................................................................159 Criegee mechanism of ozonolysis........................................................................161 Curtius rearrangement...........................................................................................162 Dakin oxidation.....................................................................................................165 Dakin-West reaction.............................................................................................167 Darzens condensation............................................................................................169 XIII Delépine amine synthesis......................................................................................171 de Mayo reaction...................................................................................................173 Demj ano v rearrangement......................................................................................175 Tiffeneau-Demjanov rearrangement............................................................177 Dess—Martin periodinane oxidation......................................................................179 Dieckmann condensation......................................................................................182 Diels-Alder reaction..............................................................................................184 Inverse electronic demand Diels-Alder reaction.........................................186 Hetero-Diels-Alder reaction........................................................................187 Dienone-phenol rearrangement............................................................................190 Di-7i-methane rearrangement................................................................................192 Doebner quinoline synthesis.................................................................................194 Doebner-von Miller reaction................................................................................196 Dötz reaction..........................................................................................................198 Dowd-Beckwith ring expansion...........................................................................200 Dudley reagent.......................................................................................................202 Erlenmeyer-Plöchl azlactone synthesis................................................................204 Eschenmoser s salt................................................................................................206 Eschenmoser-Tanabe fragmentation....................................................................208 Eschweiler-Clarke reductive alkylation of amines..............................................210 Evans aldol reaction..............................................................................................212 Favorskii rearrangement........................................................................................214 Quasi-Favorskii rearrangement.....................................................................217 Feist—Bénary furan synthesis................................................................................218 Ferner carbocyclization.........................................................................................220 Ferner glycal allylic rearrangement......................................................................222 Fiesselmann thiophene synthesis..........................................................................225 Fischer indole synthesis........................................................................................227 Fischer oxazole synthesis......................................................................................229 Fleming-Kumada oxidation.................................................................................231 Tamao-Kumada oxidation............................................................................233 Friedel-Crafts reaction..........................................................................................234 Friedel-Crafts acylation reaction..................................................................234 Friedel-Crafts alkylation reaction.................................................................236 Friedländer quinoline synthesis............................................................................238 Fries rearrangement...............................................................................................240 Fukuyama amine synthesis...................................................................................243 Fukuyama reduction..............................................................................................245 Gabriel synthesis...................................................................................................246 Ing-Manske procedure..................................................................................249 Gabriel-Colman rearrangement............................................................................250 Gassman indole synthesis......................................................................................251 Gattermann-Koch reaction...................................................................................253 Gewald aminothiophene synthesis........................................................................254 Glaser coupling......................................................................................................257 Eglinton coupling..........................................................................................259 XIV Gomberg-Bachmann reaction...............................................................................262 Gould-Jacobs reaction..........................................................................................263 Grignard reaction...................................................................................................266 Grob fragmentation...............................................................................................268 Guareschi-Thorpe condensation...........................................................................270 Hajos-Wiechert reaction.......................................................................................271 Haller-Bauer reaction...........................................................................................273 Hantzsch dihydropyridine synthesis.....................................................................274 Hantzsch pyrrole synthesis....................................................................................276 Heck reaction.........................................................................................................277 Heteroaryl Heck reaction..............................................................................280 Hegedus indole synthesis......................................................................................281 Hell-Volhard-Zelinsky reaction...........................................................................282 Henry nitroaldol reaction......................................................................................284 Hinsberg synthesis of thiophene derivatives........................................................286 Hiyama cross-coupling reaction...........................................................................288 Hofmann rearrangement.......................................................................................290 Hofmann-Löffler-Freytag reaction......................................................................292 Horner-Wadsworth-Emmons reaction................................................................294 Houben-Hoesch synthesis....................................................................................296 Hunsdiecker-Borodin reaction.............................................................................298 Jacobsen—Katsuki epoxidation..............................................................................300 Japp-Klingemann hydrazone synthesis................................................................302 Jones oxidation......................................................................................................304 Collins-Sarett oxidation................................................................................305 PCC oxidation...............................................................................................306 PDC oxidation...............................................................................................307 Julia-Kocienski olefination...................................................................................309 Julia-Lythgoe olefination.....................................................................................311 Kahne glycosidation..............................................................................................313 Knoevenagel condensation...................................................................................315 Knorr pyrazole synthesis.......................................................................................317 Koch-Haaf carbonylation.....................................................................................319 Koenig-Knorr glycosidation.................................................................................320 Kostanecki reaction...............................................................................................322 Kröhnke pyridine synthesis...................................................................................323 Kumada cross-coupling reaction...........................................................................325 Lawesson s reagent...............................................................................................328 Leuckart-Wallach reaction...................................................................................330 Lossen rearrangement...........................................................................................332 McFadyen-Stevens reduction...............................................................................334 McMurry coupling................................................................................................335 Mannich reaction...................................................................................................337 Martin s sulfurane dehydrating reagent................................................................339 Masamune-Roush conditions...............................................................................341 Meerwein s salt.....................................................................................................343 XV Meerwein-Ponndorf-Verley reduction................................................................345 Meisenheimer complex.........................................................................................347 [1,2]-Meisenheimer rearrangement......................................................................349 [2,3]-Meisenheimer rearrangement.......................................................................350 Meyers oxazoline method.....................................................................................351 Meyer-Schuster rearrangement............................................................................353 Michael addition....................................................................................................355 Michaelis-Arbuzov phosphonate synthesis..........................................................357 Midland reduction.................................................................................................359 Minisci reaction.....................................................................................................361 Mislow—Evans rearrangement...............................................................................363 Mitsunobu reaction................................................................................................365 Miyaura borylation................................................................................................368 Moffatt oxidation...................................................................................................370 Morgan-Walls reaction........................................................................................371 Mori-Ban indole synthesis....................................................................................373 Mukaiyama aldol reaction.....................................................................................375 Mukaiyama Michael addition...............................................................................377 Mukaiyama reagent...............................................................................................379 Myers-Saito cyclization........................................................................................382 Nazarov cyclization...............................................................................................383 Neber rearrangement.............................................................................................385 Nef reaction...........................................................................................................387 Negishi cross-coupling reaction............................................................................389 Nenitzescu indole synthesis..................................................................................391 Newman-Kwart reaction......................................................................................393 Nicholas reaction...................................................................................................395 Nicolaou dehydrogenation....................................................................................397 Noyori asymmetric hydrogénation........................................................................399 Nozaki-Hiyama-Kishi reaction............................................................................401 Nysted reagent.......................................................................................................403 Oppenauer oxidation.............................................................................................404 Overman rearrangement........................................................................................406 Paal thiophene synthesis........................................................................................408 Paal-Knorr turan synthesis...................................................................................409 Paal-Knorr pyrrole synthesis................................................................................411 Parham cyclization................................................................................................413 Passerini reaction...................................................................................................415 Paternö-Büchi reaction.........................................................................................417 Pauson-Khand reaction.........................................................................................419 Payne rearrangement.............................................................................................421 Pechmann coumarin synthesis..............................................................................423 Perkin reaction.......................................................................................................424 Petasis reaction......................................................................................................426 Petasis reagent.......................................................................................................428 Peterson olefination...............................................................................................430 XVI Pictet-Gams isoquinoline synthesis......................................................................432 Pictet-Spengler tetrahydroisoquinoline synthesis................................................434 Pinacol rearrangement...........................................................................................436 Pinner reaction.......................................................................................................438 Polonovski reaction...............................................................................................440 Polonovski-Potier rearrangement.........................................................................442 Pomeranz-Fritsch reaction....................................................................................444 Schüttler-Müller modification.....................................................................446 Prévost/raws-dihydroxylation..............................................................................447 Prins reaction.........................................................................................................448 Pschorr cyclization................................................................................................450 Pummerer rearrangement......................................................................................452 Ramberg-Bäcklund reaction.................................................................................454 Reformatsky reaction............................................................................................456 Regitz diazo synthesis...........................................................................................458 Reimer-Tiemann reaction.....................................................................................460 Reissert reaction....................................................................................................461 Reissert indole synthesis.......................................................................................463 Ring-closing metathesis (RCM)...........................................................................465 Ritter reaction........................................................................................................468 Robinson annulation..............................................................................................470 Robinson-Gabriel synthesis..................................................................................472 Robinson-Schöpf reaction....................................................................................474 Rosenmund reduction............................................................................................476 Rubottom oxidation...............................................................................................478 Rupe rearrangement..............................................................................................480 Saegusa oxidation..................................................................................................482 Sakurai allylation reaction....................................................................................484 Sandmeyer reaction...............................................................................................486 Schiemann reaction...............................................................................................488 Schmidt rearrangement.........................................................................................490 Schmidt s trichloroacetimidate glycosidation reaction........................................492 Shapiro reaction.....................................................................................................494 Sharpless asymmetric amino hydroxylation.........................................................496 Sharpless asymmetric dihydroxylation.................................................................499 Sharpless asymmetric epoxidation.......................................................................502 Sharpless olefin synthesis.....................................................................................505 Simmons-Smith reaction.....................................................................................507 Skraup quinoline synthesis....................................................................................509 Smiles rearrangement............................................................................................511 Truce-Smile rearrangement.........................................................................513 Sommelet reaction.................................................................................................515 Sommelet-Hauser rearrangement.........................................................................517 Sonogashira reaction.............................................................................................519 Staudinger ketene cycloaddition...........................................................................521 Staudinger reduction.............................................................................................523
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spelling	Li, Jie Jack 1964- Verfasser (DE-588)123481848 aut Name reactions a collection of detailed reaction mechanisms and synthetic applications Jie Jack Li 4., expanded ed. Berlin [u.a.] Springer 2009 XXII, 621 S. Ill., graph. Darst. txt rdacontent n rdamedia nc rdacarrier 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 (DE-588)4066724-8 Wörterbuch gnd-content Namensreaktion (DE-588)4171139-7 s Reaktionsmechanismus (DE-588)4177123-0 s 1\p DE-604 Organische Chemie (DE-588)4043793-0 s 2\p DE-604 HBZ Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=017714672&sequence=000004&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 and synthetic applications 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 and synthetic applications
title_auth	Name reactions a collection of detailed reaction mechanisms and synthetic applications
title_exact_search	Name reactions a collection of detailed reaction mechanisms and synthetic applications
title_full	Name reactions a collection of detailed reaction mechanisms and synthetic applications Jie Jack Li
title_fullStr	Name reactions a collection of detailed reaction mechanisms and synthetic applications Jie Jack Li
title_full_unstemmed	Name reactions a collection of detailed reaction mechanisms and synthetic applications Jie Jack Li
title_short	Name reactions
title_sort	name reactions a collection of detailed reaction mechanisms and synthetic applications
title_sub	a collection of detailed reaction mechanisms and synthetic applications
topic	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	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=017714672&sequence=000004&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA
work_keys_str_mv	AT lijiejack namereactionsacollectionofdetailedreactionmechanismsandsyntheticapplications

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