DEPENDENCE OF THE LEWIS ACID-INDUCED REACTION OF BETA-STANNYL KETONES UPON SUBSTITUTION PATTERN - CYCLOPROPANATION VERSUS 1,2-ALKYL MIGRATION

被引：7

作者：

FUJIWARA, J ^{[1
]}

SATO, T ^{[1
]}

机构：

[1] WASEDA UNIV, FAC SCI & ENGN,DEPT APPL CHEM,OOKUBO 3, SHINJUKU KU, TOKYO 169, JAPAN

来源：

BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN | 1993年 / 66卷 / 04期

关键词：

D O I：

10.1246/bcsj.66.1258

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

3-Stannylcyclohexanones fully substituted at 2 and 3 positions underwent a 1,2-alkyl migration, along with the cyclopropanation. The balance of the reactions depended upon the steric environment and migratory aptitude of the alkyl groups.

引用

页码：1258 / 1264

页数：7

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