Issue 7, 1974

Stereospecific synthesis of the rearrangement product obtained on reaction of penicillins with methyl chloroformate

Abstract

The product from the interesting rearrangement of penicillins with methyl chloroformate has been shown to have the structure and stereochemistry (X) by total stereospecific synthesis; this is in keeping with mechanistic considerations.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1974, 266-268

Stereospecific synthesis of the rearrangement product obtained on reaction of penicillins with methyl chloroformate

C. J. Veal and D. W. Young, J. Chem. Soc., Chem. Commun., 1974, 266 DOI: 10.1039/C39740000266

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