PALLADIUM-CATALYZED INTRAMOLECULAR ZINC-ENE REACTIONS

被引:6
|
作者
OPPOLZER, W
SCHRODER, F
机构
[1] Département de Chimie Organique, Université de Genève
关键词
D O I
10.1016/0040-4039(94)80016-2
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Cyclizations of acetoxydienes 1 with Pd(PPh(3))(4)/Et(2)Zn (0.05/4-5 mol-equiv.) in Et(2)O at reflux, followed by either protonation, iodination or cyanation, provide cis-disubstituted cyclopentanes and pyrrolidines 5, 7 or 9. These tandem reactions, as well as the conversions 15 --> 17 or 18 and 20 --> 22 show good to excellent regio- and stereocontrol, which is compared to those of Pd-ene ring closures of 1 and 20.
引用
收藏
页码:7939 / 7942
页数:4
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