CARBENOID DERIVED CARBONYL YLIDES FROM ENOLIZABLE AND NON-ENOLIZABLE KETONES-[1,4] SIGMATROPIC MIGRATION OF HYDROGEN

被引：0

作者：

LOTTES, AC ^{[1
]}

LANDGREBE, JA ^{[1
]}

机构：

[1] UNIV KANSAS,DEPT CHEM,LAWRENCE,KS 66045

来源：

ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY | 1988年 / 196卷

关键词：

D O I：

暂无

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：11 / ORGN

共 15 条

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[4] A convenient one-pot, organoaluminum mediated vinylsilane synthesis from non-enolizable ketones via the Peterson protocol
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[5] REGIOSELECTIVITY AND DIASTEREOSELECTIVITY OF ENOL ETHER FORMATION BY 1,4-SIGMATROPIC SHIFTS OF HYDROGEN IN CARBONYL YLIDES
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[6] Chemoselectivity in the Synthesis of 1,2,3-Triazoles from Enolizable Ketones, Primary Alkylamines, and 4-Nitrophenyl Azide
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[7] Catalytic [2,3]-sigmatropic rearrangement of sulfonium ylides derived from azoalkenes: non-carbenoid Doyle-Kirmse reaction
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[8] RADICAL-COUPLING PRODUCTS DERIVED FROM AMMONIUM YLIDES - COMPETING [1,2], [1,3], AND [1,4] ANIONIC REARRANGEMENTS
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OLLIS, WD
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[9] Lewis acid controlled regioselective 1,2 and 1,4 reaction of α,β-unsaturated carbonyl compounds with TiIV enolates derived from α-diazo,β-keto carbonyl compounds
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ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2002, 41 (15) : 2773 - +
[10] [1,4] and [2,3] sigmatropic rearrangements of ylides generated from N-(alpha-cyano)allyl-N-cyanomethyl-N,N-dimethylammonium perchlorates
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