MICROWAVE-INDUCED STEREOSELECTIVITY OF β-LACTAM FORMATION: EFFECTS OF SOLVENTS

Authors

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

Document Type

Article

Publication Date

2011

Abstract

Synthesis of 3, 4-disubstituted 2-azetidinones has been achieved following Staudinger reaction under microwave-induced conditions. The stereoselectivity of β-lactam formation depends on the nature of the solvents used in the reaction.

Recommended Citation

Bandyopadhyay, D., Yanez, M., & Banik, B. K. (2011). MICROWAVE-INDUCED STEREOSELECTIVITY OF β-LACTAM FORMATION: EFFECTS OF SOLVENTS. Heterocyclic Letters, 1, 65–67.

First Page

65

Last Page

67

Publication Title

Heterocyclic Letters