Stereoselectivity in ring-closing olefin metathesis (RCM) of tethered dihexenoyl derivatives

被引：20

作者：

Arisawa, M ^{[1
]}

Kaneko, H ^{[1
]}

Nishida, A ^{[1
]}

Nakagawa, M ^{[1
]}

机构：

[1] Chiba Univ, Grad Sch Pharmaceut Sci, Inage Ku, Chiba 2638522, Japan

来源：

JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1 | 2002年 / 07期

关键词：

D O I：

10.1039/b111122c

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Ring-closing olefin metatheses (RCM) of various tethered dihexenoyl derivatives were examined under various conditions. The E : Z ratios of the resulting double bonds of the cyclic products were determined. The stereochemistry of the resulting olefins was influenced largely by the effects of the template used.

引用

页码：959 / 964

页数：6

共 38 条

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