Unexpected formation of β-lactams and penem isosteres from mesoionics:: sequential ring-opening-rearrangement of [3+2] cycloadducts

被引：12

作者：

Avalos, M ^{[1
]}

Babiano, R

Cintas, P

Hursthouse, MB

Jiménez, JL

Light, ME

López, I

Palacios, JC

机构：

[1] Univ Extremadura, Fac Ciencias, Dept Quim Organ, E-06071 Badajoz, Spain

[2] Univ Southampton, Dept Chem, Southampton SO17 1BJ, Hants, England

来源：

CHEMICAL COMMUNICATIONS | 1999年 / 16期

关键词：

D O I：

10.1039/a904333k

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

A novel and simple method has been developed to obtain penem analogs with biologically interesting functionalities, which combines aromatic aldehydes with thioisomunchnones, a readily available class of mesoionic heterocycles.

引用

页码：1589 / 1590

页数：2

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