ANTI-STEREOSPECIFICITY IN THE PALLADIUM-CATALYZED REACTIONS OF ALKENYL-METAL OR ARYL-METAL DERIVATIVES WITH ALLYLIC ELECTROPHILES

被引：107

作者：

MATSUSHITA, H ^{[1
]}

NEGISHI, E ^{[1
]}

机构：

[1] PURDUE UNIV,DEPT CHEM,W LAFAYETTE,IN 47907

来源：

JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS | 1982年 / 03期

关键词：

D O I：

10.1039/c39820000160

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：160 / 161

页数：2

共 10 条

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[2] MATSUSHITA H, 1981, J AM CHEM SOC, V103, P2882, DOI 10.1021/ja00400a074
[3] SCOPE OF THE PALLADIUM-CATALYZED COUPLING REACTION OF ORGANOMETALLICS WITH ALLYLIC ELECTROPHILES - EFFECT OF THE LEAVING GROUP
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[6] NEW SYNTHETIC REACTIONS, STEREOCHEMISTRY OF ALLYLIC ALKYLATION
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[7] ALLYLIC SUBSTITUTIONS WITH RETENTION OF STEREOCHEMISTRY
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[8] ASYMMETRIC INDUCTION IN CATALYTIC ALLYLIC ALKYLATION
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[9] NEW RULES OF SELECTIVITY - ALLYLIC ALKYLATIONS CATALYZED BY PALLADIUM
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[J]. ACCOUNTS OF CHEMICAL RESEARCH, 1980, 13 (11) : 385 - 393
[10] SELECTIVE CARBON-CARBON BOND FORMATION VIA TRANSITION-METAL CATALYSIS .8. CONTROLLED CARBOMETALATION - REACTION OF ACETYLENES WITH ORGANOALANE-ZIRCONOCENE DICHLORIDE COMPLEXES AS A ROUTE TO STEREO-DEFINED AND REGIO-DEFINED TRISUBSTITUTED OLEFINS
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1978, 100 (07) : 2252 - 2254

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