Microwave-Induced Stereocontrol of β-Lactam Formation with an N-Benzylidene-9,10-dihydrophenanthren-3-amine via Staudinger Cycloaddition

被引：30

作者：

Bandyopadhyay, Debasish ^{[1
]}

Banik, Bimal K. ^{[1
]}

机构：

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

来源：

HELVETICA CHIMICA ACTA | 2010年 / 93卷 / 02期

关键词：

STEREOSELECTIVE SYNTHESIS; ORGANIC-SYNTHESIS; CHEMISTRY; CHLORIDE; IMINES; ENTRY;

D O I：

10.1002/hlca.200900212

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

The synthesis of 3-substituted 4-phenyl-1-(9,10-dihydrophenanthren-3-yl)azetidin-2-ones was achieved following Staudinger cycloaddition under microwave-induced conditions. The stereoselectivity of beta-lactam formation depended on the power level of the microwave irradiation used in the experiments.

引用

页码：298 / 301

页数：4

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