EFFECTS OF ORGANOMETALS ON THE PALLADIUM-CATALYZED TANDEM CARBOPALLADATION-CROSS COUPLING FOR PREPARING STEREODEFINED EXOCYCLIC ALKENES

被引:65
作者
NEGISHI, E
NODA, Y
LAMATY, F
VAWTER, EJ
机构
[1] Department of Chemistry, Purdue University, West Lafayette
关键词
D O I
10.1016/S0040-4039(00)97630-5
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The reaction of ω-(o-iodoaryl)- and ω-(Z-β-iodoalkenyl)alkynes with organometals containing Zr, Sn, Al, or B in the presence of a catalytic amount of a palladium-phosphine complex, such as Pd(PPh3)4, proceeds predominantly via initial cyclic carbopalladation followed by cross coupling, whereas the corresponding reaction of organozincs tends to be dominated by direct cross coupling. © 1990.
引用
收藏
页码:4393 / 4396
页数:4
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