PALLADIUM-CATALYZED VINYLATION OF ARYL CHLORIDES - CHELATE EFFECT IN CATALYSIS

被引:132
作者
BENDAVID, Y [1 ]
PORTNOY, M [1 ]
GOZIN, M [1 ]
MILSTEIN, D [1 ]
机构
[1] WEIZMANN INST SCI,DEPT ORGAN CHEM,IL-76100 REHOVOT,ISRAEL
关键词
D O I
10.1021/om00042a008
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
By use of the dippb ligand (dippb = 1,4-bis-(diisopropylphosphino)butane) it is possible to effect the synthetically useful Pd-catalyzed direct vinylation of aryl chlorides; the reaction tolerates various substituents and generally results in high yields. The reaction is very sensitive to the nature of the chelating ligand, probably as a result of the need for chelate opening to allow olefin coordination and chelate closure to promote insertion. Monophosphines are ineffective. A mechanistic scheme is presented.
引用
收藏
页码:1995 / 1996
页数:2
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