LEWIS ACID-PROMOTED [2+2]-AZETIDINE ANNULATION OF N-ACYLALDIMINES WITH ALLYLTRIISOPROPYLSILANE

被引：25

作者：

UYEHARA, T ^{[1
]}

YUUKI, M ^{[1
]}

MASAKI, H ^{[1
]}

MATSUMOTO, M ^{[1
]}

UENO, M ^{[1
]}

SATO, T ^{[1
]}

机构：

[1] TOHOKU UNIV, FAC SCI, INSTRUMENTAL ANALYT CTR CHEM, SENDAI, MIYAGI 980, JAPAN

来源：

CHEMISTRY LETTERS | 1995年 / 09期

关键词：

D O I：

10.1246/cl.1995.789

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Lewis acid-catalyzed reactions of an N-acylaldimine with allyltriisopropylsilane gave [2+2] azetidine annulation products, while those of an N-ethoxycarbonylaldimine gave an allylated product.

引用

页码：789 / 790

页数：2

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