Diastereoselective Baylis-Hillman reaction of 4-oxoazetidine-2-carbaldehydes:: rapid, stereocontrolled and divergent radical synthesis of highly functionalised β-lactams fused to medium rings

被引：38

作者：

Alcaide, B ^{[1
]}

Almendros, P ^{[1
]}

Aragoncillo, C ^{[1
]}

机构：

[1] Univ Complutense, Fac Ciencias Quim, Dept Quim Organ 1, E-28040 Madrid, Spain

来源：

CHEMICAL COMMUNICATIONS | 1999年 / 18期

关键词：

D O I：

10.1039/a905017e

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Baylis-Hillman adducts derived from enantiopure 1-alkenyl- or alkynyl-4-oxoazetidine-2-carbaldehydes are used for the stereoselective and divergent preparation of highly functionalised beta-lactams fused to medium rings through novel, chemocontrolled tandem radical addition-cyclization sequences.

引用

页码：1913 / 1914

页数：2

共 17 条

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