SYNTHESIS OF NOVEL C-4 DISUBSTITUTED beta-LACTAMS THROUGH STAUDINGER CYCLOADDITION REACTION

被引：0

作者：

Rodriguez, Robert ^{[1
]}

Nambiar, Anjali ^{[1
]}

Yadav, Ram N. ^{[1
]}

Banik, Bimal K. ^{[1
]}

机构：

[1] Univ Texas Pan Amer, Dept Chem, 1201 W Univ Dr, Edinburg, TX 78539 USA

来源：

HETEROCYCLIC LETTERS | 2014年 / 4卷 / 03期

关键词：

Cycloaddition; Imine; Pyrrole; beta-Lactam;

D O I：

暂无

中图分类号：

O62 [有机化学];

学科分类号：

070303 ; 081704 ;

摘要：

Synthesis of novel C-4 disubstituted beta-lactam that has N-methyl pyrrole system has been achieved through Staudinger cycloaddition reaction of acid chloride and imine. Interestingly, this reaction has produced a single stereoisomer.

引用

页码：417 / 419

页数：3

共 3 条

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