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

✍ Scribed by Debasish Bandyopadhyay; Bimal K. Banik


Book ID
102253754
Publisher
John Wiley and Sons
Year
2010
Tongue
German
Weight
145 KB
Volume
93
Category
Article
ISSN
0018-019X

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✦ Synopsis


Abstract

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 β‐lactam formation depended on the power level of the microwave irradiation used in the experiments.