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

Authors

Debasish Bandyopadhyay, The University of Texas Rio Grande ValleyFollow
Bimal K. Banik

Document Type

Article

Publication Date

2-11-2010

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.

Comments

Copyright © 2010 Verlag Helvetica Chimica Acta AG, Zürich, Switzerland

Recommended Citation

Bandyopadhyay, Debasish, and Bimal K. Banik. "Microwave‐Induced Stereocontrol of β‐Lactam Formation with an N‐Benzylidene‐9, 10‐dihydrophenanthren‐3‐amine via Staudinger Cycloaddition." Helvetica Chimica Acta 93.2 (2010): 298-301. https://doi.org/10.1002/hlca.200900212

Publication Title

Helvetica Chimica Acta

DOI

10.1002/hlca.200900212