Issue 0, 1971

Studies on lactams. Part XIII. A position isomer of a penam (4-thia-1-aza-bicyclo[3,2,0]heptane)

Abstract

Cycloaddition of azidoacetyl chloride and a 3-thiazoline has been used to synthesize the 6-azido-, 6-amino-, and 6-phthalimido- derivatives of a penam in which the position of the sulphur atom in the thiazolidine ring has been altered.

Article information

Article type
Paper

J. Chem. Soc. C, 1971, 188-190

Studies on lactams. Part XIII. A position isomer of a penam (4-thia-1-aza-bicyclo[3,2,0]heptane)

A. K. Bose, G. Spiegelman and M. S. Manhas, J. Chem. Soc. C, 1971, 188 DOI: 10.1039/J39710000188

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