A Suzuki cross-coupling route to substituted aziridines

被引：15

作者：

Lapinsky, DJ ^{[1
]}

Bergmeier, SC ^{[1
]}

机构：

[1] Ohio Univ, Dept Chem & Biochem, Athens, OH 45701 USA

来源：

TETRAHEDRON LETTERS | 2001年 / 42卷 / 49期

基金：

美国国家科学基金会;

关键词：

aziridines; Suzuki reactions; coupling reactions; palladium and compounds;

D O I：

10.1016/S0040-4039(01)01903-7

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

We have shown that the Suzuki cross-coupling reaction of olefinic aziridines is an effective route for the synthesis of substituted aziridines. This is the first example of a palladium coupling reaction applied to an aziridine-containing molecule. This method is complementary to other methods of aziridine synthesis utilizing organocuprate reagents. (C) 2001 Elsevier Science Ltd. All rights reserved.

引用

页码：8583 / 8586

页数：4

共 20 条

[11] Conversion of delta-(sulfonyl)amino-alpha-epoxy ketones to bicyclic ketopyrroles via intramolecular conjugate-addition to azoene intermediates. Synthesis of the bicyclic ketopyrrole core of the 1-azafulvene roseophilin. [J].