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Name Reactions
Criegee mechanism of ozonolysis
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Author(s):
Jie Jack Li
Publication date
(Online):
January 4 2014
Publisher:
Springer International Publishing
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Preparation, properties, and reactions of carbonyl oxides
William Bunnelle
(1991)
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Oxidative cleavage of mono-, di-, and trisubstituted olefins to methyl esters through ozonolysis in methanolic sodium hydroxide
James A R Marshall
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Albert Garofalo
(1993)
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The structure and mechanism of formation of ozonides
Robert L. Kuczkowski
(1992)
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Book Chapter
Publication date (Print):
2014
Publication date (Online):
January 4 2014
Page
: 187
DOI:
10.1007/978-3-319-03979-4_77
SO-VID:
9d57c232-7e7d-42d2-812f-33cc74b6738f
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Book chapters
pp. 1
Alder ene reaction
pp. 3
Aldol condensation
pp. 6
Algar–Flynn–Oyamada Reaction
pp. 8
Allan–Robinson reaction
pp. 10
Arndt–Eistert homologation
pp. 12
Baeyer–Villiger oxidation
pp. 14
Baker–Venkataraman rearrangement
pp. 16
Bamford–Stevens reaction
pp. 18
Baran reagents
pp. 21
Barbier reaction
pp. 23
Bargellini reaction
pp. 24
Bartoli indole synthesis
pp. 26
Barton radical decarboxylation
pp. 28
Barton–McCombie deoxygenation
pp. 30
Barton nitrite photolysis
pp. 32
Barton–Zard reaction
pp. 34
Batcho–Leimgruber indole synthesis
pp. 36
Baylis–Hillman reaction
pp. 39
Beckmann rearrangement
pp. 42
Beirut reaction
pp. 44
Benzilic acid rearrangement
pp. 46
Benzoin condensation
pp. 48
Bergman cyclization
pp. 50
Biginelli reaction
pp. 52
Birch reduction
pp. 54
Bischler–Möhlau indole synthesis
pp. 56
Bischler–Napieralski reaction
pp. 58
Blaise reaction
pp. 60
Blum–Ittah aziridine synthesis
pp. 62
Boekelheide reaction
pp. 64
Boger pyridine synthesis
pp. 66
Borch reductive amination
pp. 68
Borsche–Drechsel cyclization
pp. 70
Boulton–Katritzky rearrangement
pp. 72
Bouveault aldehyde synthesis
pp. 74
Bouveault–Blanc reduction
pp. 75
Boyland–Sims oxidation
pp. 77
Bradsher reaction
pp. 79
Brook rearrangement
pp. 81
Brown hydroboration
pp. 83
Bucherer carbazole synthesis
pp. 85
Bucherer reaction
pp. 87
Bucherer–Bergs reaction
pp. 89
Büchner ring expansion
pp. 91
Buchwald–Hartwig amination
pp. 95
Burgess reagent
pp. 97
Burke boronates
pp. 100
Cadiot–Chodkiewicz coupling
pp. 102
Cadogan–Sundberg indole synthesis
pp. 104
Camps quinoline synthesis
pp. 106
Cannizzaro reaction
pp. 108
Carroll rearrangement
pp. 110
Castro–Stephens coupling
pp. 112
C–H activation
pp. 123
Chan alkyne reduction
pp. 125
Chan–Lam C–X coupling reaction
pp. 128
Chapman rearrangement
pp. 130
Chichibabin pyridine synthesis
pp. 133
Chugaev elimination
pp. 135
Ciamician–Dennsted rearrangement
pp. 136
Claisen condensation
pp. 138
Claisen isoxazole synthesis
pp. 140
Claisen rearrangements
pp. 153
Clemmensen reduction
pp. 155
Combes quinoline synthesis
pp. 157
Conrad–Limpach reaction
pp. 159
Cope elimination reaction
pp. 161
Cope rearrangement
pp. 168
Corey–Bakshi–Shibata (CBS) reagent
pp. 171
Corey–Chaykovsky reaction
pp. 174
Corey–Fuchs reaction
pp. 176
Corey–Kim oxidation
pp. 178
Corey–Nicolaou macrolactonization
pp. 180
Corey–Seebach reaction
pp. 182
Corey–Winter olefin synthesis
pp. 185
Criegee glycol cleavage
pp. 187
Criegee mechanism of ozonolysis
pp. 188
Curtius rearrangement
pp. 190
Dakin oxidation
pp. 192
Dakin–West reaction
pp. 194
Danheiser annulation
pp. 196
Darzens condensation
pp. 198
Delépine amine synthesis
pp. 200
de Mayo reaction
pp. 202
Demjanov rearrangement
pp. 206
Dess–Martin periodinane oxidation
pp. 209
Dieckmann condensation
pp. 211
Diels–Alder reaction
pp. 217
Dienone–phenol rearrangement
pp. 219
Doebner quinoline synthesis
pp. 221
Doebner–von Miller reaction
pp. 223
Dötz reaction
pp. 225
Dowd–Beckwith ring expansion
pp. 227
Dudley reagent
pp. 229
Erlenmeyer–Plöchl azlactone synthesis
pp. 231
Eschenmoser’s salt
pp. 233
Eschenmoser–Tanabe fragmentation
pp. 235
Eschweiler–Clarke reductive alkylation of amines
pp. 237
Evans aldol reaction
pp. 239
Favorskii rearrangement
pp. 243
Feist–Bénary furan synthesis
pp. 245
Ferrier carbocyclization
pp. 247
Ferrier glycal allylic rearrangement
pp. 250
Fiesselmann thiophene synthesis
pp. 252
Fischer–Speier esterification
pp. 253
Fischer indole synthesis
pp. 255
Fischer oxazole synthesis
pp. 257
Fleming–Kumada oxidation
pp. 260
Friedel–Crafts reaction
pp. 264
Friedländer quinoline synthesis
pp. 266
Fries rearrangement
pp. 268
Fukuyama amine synthesis
pp. 270
Fukuyama reduction
pp. 272
Gabriel synthesis
pp. 275
Gabriel–Colman rearrangement
pp. 276
Gassman indole synthesis
pp. 278
Gattermann–Koch reaction
pp. 279
Gewald aminothiophene synthesis
pp. 282
Glaser coupling
pp. 287
Gomberg–Bachmann reaction
pp. 289
Gould–Jacobs reaction
pp. 291
Grignard reaction
pp. 293
Grob fragmentation
pp. 295
Guareschi–Thorpe condensation
pp. 297
Hajos–Wiechert reaction
pp. 299
Haller–Bauer reaction
pp. 300
Hantzsch dihydropyridine synthesis
pp. 302
Hantzsch pyrrole synthesis
pp. 304
Heck reaction
pp. 309
Hegedus indole synthesis
pp. 310
Hell–Volhard–Zelinsky reaction
pp. 312
Henry nitroaldol reaction
pp. 314
Hinsberg synthesis of thiophenes
pp. 316
Hiyama cross-coupling reaction
pp. 318
Hofmann elimination
pp. 319
Hofmann rearrangement
pp. 321
Hofmann–Löffler–Freytag reaction
pp. 323
Horner–Wadsworth–Emmons reaction
pp. 325
Houben–Hoesch reaction
pp. 327
Hunsdiecker–Borodin reaction
pp. 329
Jacobsen–Katsuki epoxidation
pp. 331
Japp–Klingemann hydrazone synthesis
pp. 333
Jones oxidation
pp. 338
Julia–Kocienski olefination
pp. 340
Julia–Lythgoe olefination
pp. 342
Kahne glycosidation
pp. 344
Knoevenagel condensation
pp. 347
Knorr pyrazole synthesis
pp. 349
Koch–Haaf carbonylation
pp. 350
Koenig–Knorr glycosidation
pp. 353
Kostanecki reaction
pp. 354
Kröhnke pyridine synthesis
pp. 356
Krapcho reaction
pp. 357
Kumada cross-coupling reaction
pp. 360
Lawesson’s reagent
pp. 362
Leuckart–Wallach reaction
pp. 364
Li A3 reaction
pp. 367
Lossen rearrangement
pp. 369
McFadyen–Stevens reduction
pp. 370
McMurry coupling
pp. 372
MacMillan catalyst
pp. 374
Mannich reaction
pp. 376
Markovnikov’s rule
pp. 379
Martin’s sulfurane dehydrating reagent
pp. 382
Masamune–Roush conditions for the Horner–Emmons reaction
pp. 384
Meerwein’s salt
pp. 386
Meerwein–Ponndorf–Verley reduction
pp. 388
Meisenheimer complex
pp. 390
[1,2]-Meisenheimer rearrangement
pp. 391
[2,3]-Meisenheimer rearrangement
pp. 393
Meyers oxazoline method
pp. 395
Meyer–Schuster rearrangement
pp. 397
Michael addition
pp. 399
Michaelis–Arbuzov phosphonate synthesis
pp. 401
Midland reduction
pp. 403
Minisci reaction
pp. 405
Mislow–Evans rearrangement
pp. 407
Mitsunobu reaction
pp. 409
Miyaura borylation
pp. 411
Moffatt oxidation
pp. 413
Morgan–Walls reaction
pp. 415
Mori–Ban indole synthesis
pp. 417
Mukaiyama aldol reaction
pp. 419
Mukaiyama Michael addition
pp. 421
Mukaiyama reagent
pp. 423
Myers–Saito cyclization
pp. 424
Nazarov cyclization
pp. 426
Neber rearrangement
pp. 428
Nef reaction
pp. 430
Negishi cross-coupling reaction
pp. 432
Nenitzescu indole synthesis
pp. 434
Newman–Kwart rearrangement
pp. 436
Nicholas reaction
pp. 438
Nicolaou IBX dehydrogenation
pp. 440
Noyori asymmetric hydrogenation
pp. 443
Nozaki–Hiyama–Kishi reaction
pp. 445
Nysted reagent
pp. 447
Oppenauer oxidation
pp. 449
Overman rearrangement
pp. 451
Paal thiophene synthesis
pp. 452
Paal–Knorr furan synthesis
pp. 454
Paal–Knorr pyrrole synthesis
pp. 456
Parham cyclization
pp. 458
Passerini reaction
pp. 460
Paternó–Büchi reaction
pp. 462
Pauson–Khand reaction
pp. 464
Payne rearrangement
pp. 466
Pechmann coumarin synthesis
pp. 468
Perkin reaction
pp. 470
Perkow vinyl phosphate synthesis
pp. 472
Petasis reaction
pp. 474
Petasis reagent
pp. 476
Peterson olefination
pp. 478
Pictet–Gams isoquinoline synthesis
pp. 480
Pictet–Spengler tetrahydroisoquinoline synthesis
pp. 482
Pinacol rearrangement
pp. 484
Pinner reaction
pp. 486
Polonovski reaction
pp. 488
Polonovski–Potier reaction
pp. 490
Pomeranz–Fritsch reaction
pp. 493
Pavorov reaction
pp. 495
Prévost trans-dihydroxylation
pp. 496
Prins reaction
pp. 499
Pschorr cyclization
pp. 501
Pummerer rearrangement
pp. 503
Ramberg–Bäcklund reaction
pp. 505
Reformatsky reaction
pp. 507
Regitz diazo synthesis
pp. 509
Reimer–Tiemann reaction
pp. 510
Reissert reaction
pp. 512
Reissert indole synthesis
pp. 514
Ring-closing metathesis (RCM)
pp. 517
Ritter reaction
pp. 519
Robinson annulation
pp. 521
Robinson–Gabriel synthesis
pp. 523
Robinson–Schöpf reaction
pp. 525
Rosenmund reduction
pp. 527
Rubottom oxidation
pp. 529
Rupe rearrangement
pp. 531
Saegusa oxidation
pp. 533
Sakurai allylation reaction
pp. 535
Sandmeyer reaction
pp. 537
Schiemann reaction
pp. 539
Schmidt rearrangement
pp. 541
Schmidt’s trichloroacetimidate glycosidation
pp. 543
Scholl reaction
pp. 544
Shapiro reaction
pp. 546
Sharpless asymmetric amino-hydroxylation
pp. 549
Sharpless asymmetric dihydroxylation
pp. 552
Sharpless asymmetric epoxidation
pp. 555
Sharpless olefin synthesis
pp. 557
Shi asymmetric epoxidation
pp. 560
Simmons–Smith reaction
pp. 562
Skraup quinoline synthesis
pp. 564
Smiles rearrangement
pp. 568
Sommelet reaction
pp. 570
Sommelet–Hauser rearrangement
pp. 572
Sonogashira reaction
pp. 574
Staudinger ketene cycloaddition
pp. 576
Staudinger reduction
pp. 578
Stetter reaction
pp. 580
Stevens rearrangement
pp. 582
Still–Gennari phosphonate reaction
pp. 584
Stille coupling
pp. 586
Stille–Kelly rea ction
pp. 587
Stobbe condensation
pp. 589
Stork–Danheiser transposition
pp. 591
Strecker amino acid synthesis
pp. 593
Suzuki–Miyaura coupling
pp. 595
Swern oxidation
pp. 597
Takai reaction
pp. 599
Tebbe reagent
pp. 601
TEMPO oxidation
pp. 603
Thorpe–Ziegler reaction
pp. 605
Tsuji–Trost reaction
pp. 608
Ugi reaction
pp. 611
Ullmann coupling
pp. 613
van Leusen oxazole synthesis
pp. 615
Vilsmeier–Haack reaction
pp. 617
Vinylcyclopropane–cyclopentene rearrangement
pp. 619
von Braun reaction
pp. 620
Wacker oxidation
pp. 622
Wagner–Meerwein rearrangement
pp. 624
Weiss–Cook condensation
pp. 626
Wharton reaction
pp. 628
Williamson ether synthesis
pp. 629
Willgerodt–Kindler reaction
pp. 632
Wittig reaction
pp. 636
[1,2]-Wittig rearrangement
pp. 638
[2,3]-Wittig rearrangement
pp. 640
Wohl–Ziegler reaction
pp. 642
Wolff rearrangement
pp. 644
Wolff–Kishner reduction
pp. 646
Woodward cis-dihydroxylation
pp. 648
Yamaguchi esterification
pp. 650
Zaitsev’s elimination rule
pp. 652
Zhang enyne cycloisomerization
pp. 654
Zimmerman rearrangement
pp. 656
Zincke reaction
pp. 659
Zinin benzidine (semidne) rearrangement
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