Issue 8, 1969

Isolation of a bicyclo[3,1,0]hexan-3-one on photolysis of a cyclohexa-2,5-dienone: direct evidence for a zwitterion intermediate

Abstract

A bicyclo[3,1,0]hexan-3-one derivative, formed on photolysis of 4-methyl-4-trichloromethyl cyclohexa-2,5-dienone, is the first dienone photo-product in which the carbon skeleton of the previously postulated zwitterion intermediate has been trapped intact.

Article information

Article type
Paper

J. Chem. Soc. D, 1969, 419-420

Isolation of a bicyclo[3,1,0]hexan-3-one on photolysis of a cyclohexa-2,5-dienone: direct evidence for a zwitterion intermediate

D. I. Schuster and V. Y. Abraitys, J. Chem. Soc. D, 1969, 419 DOI: 10.1039/C29690000419

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