Issue 2, 1982

An efficient stereoselective method for the synthesis of thienamycin intermediates

Abstract

A three-step procedure for the synthesis of trans-3,4-disubstituted azetidin-2-ones which utilizes 1,3-dipolar cycloaddition as the key step has led to the synthesis of the azetidinones (16) and (17)

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1982, 104-105

An efficient stereoselective method for the synthesis of thienamycin intermediates

R. V. Stevens and K. Albizati, J. Chem. Soc., Chem. Commun., 1982, 104 DOI: 10.1039/C39820000104

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