17:
151:
Sharpless, K. Barry; Young, Michael W. (1975). "Olefin synthesis. Rate enhancement of the elimination of alkyl aryl selenoxides by electron-withdrawing substituents".
123:
Grieco, Paul A.; Gilman, Sydney; Nishizawa, Mugio (1976). "Organoselenium chemistry. A facile one-step synthesis of alkyl aryl selenides from alcohols".
100:
479:
464:
225:
188:
509:
106:
The elimination step is common with the Clive-Reich-Sharpless olefination that uses PhSeX as the selenium source.
661:
656:
439:
444:
635:
68:
16:
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181:
Organic
Syntheses Based on Name Reactions: A Practical Guide to Over 800 Transformations
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99:. This reaction takes part in the synthesis of ring C of the
203:
122:
83:. This structure decomposes to form an alkene by an
75:. In the second step, the selenide is oxidized with
178:
648:
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219:
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212:
649:
207:
179:Hassner, A.; Namboothiri, I. (2011).
95:in a fashion similar to that of the
13:
15:
14:
678:
480:Horner–Wadsworth–Emmons reaction
172:
144:
116:
59:-nitrophenylselenocyanate and
55:The alcohol first reacts with
1:
465:Corey–Winter olefin synthesis
109:
183:(3rd ed.). p. 91.
7:
233:
101:Danishefsky Taxol synthesis
10:
683:
71:on the electron-deficient
636:Friedel-Crafts Alkylation
548:
510:Ramberg–Bäcklund reaction
405:
241:
69:nucleophilic substitution
440:Bamford–Stevens reaction
576:Oxymercuration reaction
445:Barton–Kellogg reaction
571:Electrophilic addition
450:Boord olefin synthesis
21:
20:The Grieco elimination
662:Olefination reactions
657:Elimination reactions
495:Kauffmann olefination
89:elimination mechanism
19:
616:Diels–Alder reaction
505:Peterson olefination
485:Hydrazone iodination
422:Dehydration reaction
91:with expulsion of a
34:elimination reaction
475:Hofmann elimination
455:Chugaev elimination
413:Dehydrohalogenation
166:10.1021/jo00895a030
138:10.1021/jo00870a052
540:Cope rearrangement
470:Grieco elimination
48:. It is named for
26:Grieco elimination
22:
644:
643:
606:Hydrohalogenation
530:Olefin metathesis
520:Takai olefination
490:Julia olefination
431:Semihydrogenation
77:hydrogen peroxide
61:tributylphosphine
674:
586:Cyclopropanation
515:Shapiro reaction
500:McMurry reaction
397:
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132:(8): 1485–1486.
120:
97:Cope elimination
36:of an aliphatic
30:organic reaction
682:
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626:Dehydrogenation
596:Dihydroxylation
544:
525:Wittig reaction
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46:terminal alkene
38:primary alcohol
32:describing the
12:
11:
5:
680:
670:
669:
667:Name reactions
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623:
621:Wacker process
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611:Polymerization
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160:(7): 947–949.
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581:Hydroboration
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556:Hydrogenation
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460:Cope reaction
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190:9780080966311
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154:J. Org. Chem.
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126:J. Org. Chem.
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631:Ene reaction
561:Halogenation
535:Ene reaction
469:
406:Preparations
200:
180:
174:
157:
152:
146:
129:
124:
118:
105:
56:
54:
25:
23:
591:Epoxidation
50:Paul Grieco
651:Categories
601:Ozonolysis
417:haloalkane
110:References
81:selenoxide
79:to give a
63:to form a
40:through a
566:Hydration
549:Reactions
73:selenium
65:selenide
42:selenide
426:alcohol
334:Heptene
300:Pentene
266:Propene
242:Alkenes
235:Alkenes
93:selenol
435:alkyne
385:Decene
368:Nonene
351:Octene
317:Hexene
283:Butene
249:Ethene
187:
67:via a
28:is an
433:from
424:from
415:from
44:to a
185:ISBN
24:The
162:doi
134:doi
653::
395:20
391:10
378:18
361:16
344:14
327:12
310:10
158:40
130:41
103:.
52:.
398:)
393:H
389:C
387:(
381:)
376:H
374:9
372:C
370:(
364:)
359:H
357:8
355:C
353:(
347:)
342:H
340:7
338:C
336:(
330:)
325:H
323:6
321:C
319:(
313:)
308:H
306:5
304:C
302:(
296:)
293:8
291:H
289:4
287:C
285:(
279:)
276:6
274:H
272:3
270:C
268:(
262:)
259:4
257:H
255:2
253:C
251:(
227:e
220:t
213:v
193:.
168:.
164::
140:.
136::
87:i
85:E
57:o
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