Name reactions: a collection of detailed mechanisms and synthetic applications
Gespeichert in:
| 1. Verfasser: | |
|---|---|
| Format: | Buch |
| Sprache: | English |
| Veröffentlicht: |
Cham
Springer
2014
|
| Ausgabe: | 5. ed. |
| Schlagworte: | |
| Online-Zugang: | Inhaltstext Inhaltsverzeichnis |
| Beschreibung: | XXII, 681 S. graph. Darst. |
| ISBN: | 3319039784 9783319039787 |
Internformat
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Datensatz im Suchindex
| _version_ | 1806327838424432640 |
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| adam_text |
Titel: Name reactions
Autor: Li, Jie Jack
Jahr: 2014
Table of Contents
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
Baran reagents.18
Barbier reaction.21
Bargellini reaction.23
Bartoli indole synthesis.24
Barton radical decarboxylation.26
Barton-McCombie deoxygenation.28
Barton nitrite photolysis.30
Barton-Zard reaction.32
Batcho-Leimgraber indole synthesis.34
Baylis-Hillman reaction.36
Beckmann rearrangement.39
Abnormal Beckmann rearrangement.40
Beirut reaction.42
Benzilic acid rearrangement.44
Benzoin condensation.46
Bergman cyclization.48
Biginelli reaction.50
Birch reduction.52
Bischler-Möhlau indole synthesis.54
xii Table of Contents
Bischler-Napieralski reaction.56
Blaise reaction.58
Blum-Ittah aziridine synthesis.60
Boekelheide reaction.62
Boger pyridine synthesis.64
Borch reductive amination.66
Borsche-Drechsel cyclization.68
Boulton-Katritzky rearrangement.70
Bouveault aldehyde synthesis.72
Bouveault-Blanc reduction.74
Boyland-Sims oxidation.75
Elbs oxidation.76
Bradsher reaction.77
Brook rearrangement.79
Brown hydroboration.81
Bucherer carbazole synthesis.83
Bucherer reaction.85
Bucherer-Bergs reaction.87
Büchner ring expansion.89
Buchwald-Hartwig amination.91
Burgess reagent.95
Burke boronates.97
Cadiot-Chodkiewicz coupling.100
Cadogan-Sundberg indole synthesis.102
Camps quinoline synthesis.104
Cannizzaro reaction.106
Carroll rearrangement.108
Castro-Stephens coupling.110
C-H activation.112
Catellani reaction.112
Sanford reaction.115
White catalyst.117
Yu C-H activation.121
Chan alkyne reduction.123
Chan-Lam C-X coupling reaction.125
Chapman rearrangement.128
Chichibabin pyridine synthesis.130
Chugaev elimination.133
Ciamician-Dennsted rearrangement.135
Claisen condensation.136
Claisen isoxazole synthesis.138
Claisen rearrangements.140
/?ara-Claisen rearrangement.142
Abnormal Claisen rearrangement.144
Table of Contents xiii
Eschenmoser-Claisen amide acetal rearrangement.146
Ireland-Claisen (silyl ketene acetal) rearrangement.148
Johnson-Claisen (orthoester) rearrangement.150
Clemmensen reduction.153
Combes quinoline synthesis.155
Conrad-Limpach reaction.157
Cope elimination reaction.159
Cope rearrangement.161
Anionic oxy-Cope rearrangement.163
Oxy-Cope rearrangement.164
Siloxy-Cope rearrangement.166
Corey-Bakshi-Shibata (CBS) reagent.168
Corey-Chaykovsky reaction.171
Corey-Fuchs reaction.174
Corey-Kim oxidation.176
Corey-Nicolaoumacrolactonization.178
Corey-Seebach reaction.180
Corey-Winter olefin synthesis.182
Criegee glycol cleavage.185
Criegee mechanism of ozonolysis.187
Curtius rearrangement.188
Dakin oxidation.190
Dakin-West reaction.192
Danheiser annulation.194
Darzens condensation.196
Delépine amine synthesis.198
de Mayo reaction.200
Demjanov rearrangement.202
Tiffeneau-Demjanov rearrangement.203
Dess-Martin periodinane oxidation.206
Dieckmann condensation.209
Diels-Alder reaction.211
Inverse electronic demand Diels-Alder reaction.213
Hetero-Diels-Alder reaction.215
Dienone-phenol rearrangement.217
Doebner quinoline synthesis.219
Doebner-von Miller reaction.221
Dötz reaction.223
Dowd-Beckwith ring expansion.225
Dudley reagent.¡.227
Erlenmeyer-Plöchl azlactone synthesis.229
Eschenmoser's salt.231
Eschenmoser-Tanabe fragmentation.233
Eschweiler-Clarke reductive alkylation of amines.235
xiv Table of Contents
Evans aldol reaction.237
Favorskii rearrangement.239
Quasi-Favorskii rearrangement.242
Feist-Bénary furan synthesis.243
Ferrier carbocyclization.245
Ferrier glycal allylic rearrangement.247
Fiesselmann thiophene synthesis.250
Fischer-Speier esterification.252
Fischer indole synthesis.253
Fischer oxazole synthesis.255
Fleming-Kumada oxidation.257
Tamao-Kumada oxidation.259
Friedel-Crafts reaction.260
Friedel-Crafts acylation reaction.260
Friedel-Crafts alkylation reaction.262
Friedländer quinoline synthesis.264
Fries rearrangement.266
Fukuyama amine synthesis.268
Fukuyama reduction.270
Gabriel synthesis.272
Ing-Manske procedure.273
Gabriel-Colman rearrangement.275
Gassman indole synthesis.276
Gattermann-Koch reaction.278
Gewald aminothiophene synthesis.279
Glaser coupling.282
Eglinton coupling.284
Gomberg-Bachmann reaction.287
Gould-Jacobs reaction.289
Grignard reaction.291
Grob fragmentation.293
Guareschi-Thorpe condensation.295
Hajos-Wiechert reaction.297
Haller-Bauer reaction.299
Hantzsch dihydropyridine synthesis.300
Hantzsch pyrrole synthesis.302
Heck reaction.304
Heteroaryl Heck reaction.307
Hegedus indole synthesis.309
Hell-Volhard-Zelinsky reaction.310
Henry nitroaldol reaction.312
Hinsberg synthesis of thiophenes.314
Hiyama cross-coupling reaction.316
Hofmann elimination.318
Table of Contents xv
Hofmann rearrangement.319
Hofmann-Löffler-Freytag reaction.321
Horner-Wadsworfh-Emmons reaction.323
Houben-Hoesch reaction.325
Hunsdiecker-Borodin reaction.327
Jacobsen-Katsuki epoxidation.329
Japp-Klingemann hydrazone synthesis.331
Jones oxidation.333
Collins oxidation.335
PCC oxidation.336
PDC oxidation.337
Julia-Kocienski olefination.338
Julia-Lythgoe olefination.340
Kahne glycosidation.342
Knoevenagel condensation.344
Knorr pyrazole synthesis.347
Koch-Haaf carbonylation.349
Koenig-Knorr glycosidation.350
Kostanecki reaction.353
Kröhnke pyridine synthesis.354
Krapcho reaction.356
Kumada cross-coupling reaction.357
Lawesson's reagent.360
Leuckart-Wallach reaction.362
Li A3 reaction.364
Lossen rearrangement.367
McFadyen-Stevens reduction.369
McMurry coupling.370
MacMillan catalyst.372
Mannich reaction.374
Markovnikov's rule.376
Anti-Markovnikov.377
Martin's sulfurane dehydrating reagent.379
Masamune-Roush conditions for the Horner-Emmons reaction.382
Meerwein's salt.384
Meerwein-Ponndorf-Verley reduction.386
Meisenheimer complex.388
[1,2]-Meisenheimer rearrangement.390
[2,3]-Meisenheimer rearrangement.391
Meyers oxazoline method.393
Meyer-Schuster rearrangement.395
Michael addition.397
Michaelis-Arbuzov phosphonate synthesis.399
Midland reduction.401
xvi Table of Contents
Minisei reaction.403
Mislow-Evans rearrangement.405
Mitsunobu reaction.407
Miyaura borylation.409
Moffatt oxidation.411
Morgan-Walls reaction.413
Pietet-Hubert reaction.413
Mori-Ban indole synthesis.415
Mukaiyama aldol reaction.417
Mukaiyama Michael addition.419
Mukaiyama reagent.421
Myers-Saito cyclization.423
Nazarov cyclization.424
Neber rearrangement.426
Nef reaction.428
Negishi cross-coupling reaction.430
Nenitzescu indole synthesis.432
Newman-Kwart rearrangement.434
Nicholas reaction.436
Nicolaou IBX dehydrogenation.438
Noyori asymmetric hydrogénation.440
Nozaki-Hiyama-Kishi reaction.443
Nysted reagent.445
Oppenauer oxidation.447
Overman rearrangement.449
Paal thiophene synthesis.451
Paal-Knorr furan synthesis.452
Paal-Knorr pyrrole synthesis.454
Parham cyclization.456
Passerini reaction.458
Paternó-Büchi reaction.460
Pauson-Khand reaction.462
Payne rearrangement.464
Pechmann coumarin synthesis.466
Perkin reaction.468
Perkow vinyl phosphate synthesis.470
Petasis reaction.472
Petasis reagent.474
Peterson olefination.476
Pictet-Gams isoquinoline synthesis.478
Pictet-Spengler tetrahydroisoquinoline synthesis.480
Pinacol rearrangement.482
Pinner reaction.484
Polonovski reaction.486
Table of Contents xvii
Polonovski-Potier reaction.488
Pomeranz-Fritsch reaction.490
Schlittler-Müller modification.492
Pavorov reaction.493
Prévost ¿røtts-dihydroxylation.495
Prins reaction.496
Pschorr cyclization.499
Pummerer rearrangement.501
Ramberg-Bäcklund reaction.503
Reformatsky reaction.505
Regitz diazo synthesis.507
Reimer-Tiemann reaction.509
Reissert reaction.510
Reissert indole synthesis.512
Ring-closing metathesis (RCM).514
Ritter reaction.517
Robinson annulation.519
Robinson-Gabriel synthesis.521
Robinson-Schöpf reaction.523
Rosenmund reduction.525
Rubottom oxidation.527
Rupe rearrangement.529
Saegusa oxidation.531
Sakurai allylation reaction.533
Sandmeyer reaction.535
Schiemann reaction.537
Schmidt rearrangement.539
Schmidt's trichloroacetimidate glycosidation.541
Scholl reaction.543
Shapiro reaction.544
Sharpless asymmetric amino hydroxylation.546
Sharpless asymmetric dihydroxylation.549
Sharpless asymmetric epoxidation.552
Sharpless olefin synthesis.555
Shi asymmetric epoxidation.557
Simmons-Smith reaction.560
Skraup quinoline synthesis.562
Smiles rearrangement.564
Truce-Smile rearrangement.566
Sommelet reaction.568
Sommelet-Hauser rearrangement.570
Sonogashira reaction.572
Staudinger ketene cycloaddition.574
Staudinger reduction.576
xviii Table of Contents
Stetter reaction.578
Stevens rearrangement.580
Stili-Gennari phosphonate reaction.582
Stille coupling.584
Stille-Kelly reaction.586
Stobbe condensation.587
Stork-Danheiser transposition.589
Strecker amino acid synthesis.591
Suzuki-Miyaura coupling.593
Swern oxidation.595
Takai reaction.597
Tebbe reagent.599
TEMPO oxidation.601
Thorpe-Ziegler reaction.603
Tsuji-Trost reaction.605
Ugi reaction.608
Ullmann coupling.611
van Leusen oxazole synthesis.613
Vilsmeier-Haack reaction.615
Vinylcyclopropane-cyclopentene rearrangement.617
von Braun reaction.619
Wacker oxidation.620
Wagner-Meerwein rearrangement.622
Weiss-Cook condensation.624
Wharton reaction.626
Williamson ether synthesis.628
Willgerodt-Kindler reaction.629
Wittig reaction.632
Schlosser modification of the Wittig reaction.634
[1,2]-Wittig rearrangement.636
[2,3]-Wittig rearrangement.638
Wohl-Ziegler reaction.640
Wolff rearrangement.642
Wolff-Kishner reduction.644
Woodward c/s-dihydroxylation.646
Yamaguchi esterification.648
Zaitsev's elimination rale.650
Zhang enyne cycloisomerization.652
Zimmerman rearrangement.654
Zincke reaction.656
Zinin benzidine (semidne) rearrangement.659
Index.661 |
| 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 | BV041831365 |
| classification_rvk | VK 6003 |
| classification_tum | CHE 608b CHE 620b |
| ctrlnum | (OCoLC)881138726 (DE-599)DNB1044794941 |
| discipline | Chemie / Pharmazie Chemie |
| edition | 5. ed. |
| format | Book |
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| id | DE-604.BV041831365 |
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| indexdate | 2024-08-03T01:27:44Z |
| institution | BVB |
| isbn | 3319039784 9783319039787 |
| language | English |
| oai_aleph_id | oai:aleph.bib-bvb.de:BVB01-027276241 |
| oclc_num | 881138726 |
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| physical | XXII, 681 S. graph. Darst. |
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| publisher | Springer |
| record_format | marc |
| spelling | Li, Jie Jack 1964- Verfasser (DE-588)123481848 aut Name reactions a collection of detailed mechanisms and synthetic applications Jie Jack Li 5. ed. Cham Springer 2014 XXII, 681 S. graph. Darst. txt rdacontent n rdamedia nc rdacarrier Reaktionsmechanismus (DE-588)4177123-0 gnd rswk-swf Namensreaktion (DE-588)4171139-7 gnd rswk-swf Organische Chemie (DE-588)4043793-0 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 Erscheint auch als Online-Ausgabe 978-3-319-03979-4 X:MVB text/html http://deposit.dnb.de/cgi-bin/dokserv?id=4528657&prov=M&dok_var=1&dok_ext=htm Inhaltstext HBZ Datenaustausch application/pdf http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=027276241&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 mechanisms and synthetic applications Reaktionsmechanismus (DE-588)4177123-0 gnd Namensreaktion (DE-588)4171139-7 gnd Organische Chemie (DE-588)4043793-0 gnd |
| subject_GND | (DE-588)4177123-0 (DE-588)4171139-7 (DE-588)4043793-0 (DE-588)4066724-8 |
| title | Name reactions a collection of detailed mechanisms and synthetic applications |
| title_auth | Name reactions a collection of detailed mechanisms and synthetic applications |
| title_exact_search | Name reactions a collection of detailed mechanisms and synthetic applications |
| title_full | Name reactions a collection of detailed mechanisms and synthetic applications Jie Jack Li |
| title_fullStr | Name reactions a collection of detailed mechanisms and synthetic applications Jie Jack Li |
| title_full_unstemmed | Name reactions a collection of detailed mechanisms and synthetic applications Jie Jack Li |
| title_short | Name reactions |
| title_sort | name reactions a collection of detailed mechanisms and synthetic applications |
| title_sub | a collection of detailed mechanisms and synthetic applications |
| topic | Reaktionsmechanismus (DE-588)4177123-0 gnd Namensreaktion (DE-588)4171139-7 gnd Organische Chemie (DE-588)4043793-0 gnd |
| topic_facet | Reaktionsmechanismus Namensreaktion Organische Chemie Wörterbuch |
| url | http://deposit.dnb.de/cgi-bin/dokserv?id=4528657&prov=M&dok_var=1&dok_ext=htm http://bvbr.bib-bvb.de:8991/F?func=service&doc_library=BVB01&local_base=BVB01&doc_number=027276241&sequence=000001&line_number=0001&func_code=DB_RECORDS&service_type=MEDIA |
| work_keys_str_mv | AT lijiejack namereactionsacollectionofdetailedmechanismsandsyntheticapplications |