Issue 10, 1969

Cyclohexadienones: stereospecific photochemical rearrangements of o-quinol acetates

Abstract

The photochemically-induced rearrangement of some cyclohexa-2,4-dienones to bicyclo[3,1,0]hex-3-en-2-ones occurs by a general stereospecific ring opening to a keten, which is followed by a stereospecific thermal cyclisation.

Article information

Article type
Paper

J. Chem. Soc. D, 1969, 526-527

Cyclohexadienones: stereospecific photochemical rearrangements of o-quinol acetates

M. R. Morris and A. J. Waring, J. Chem. Soc. D, 1969, 526 DOI: 10.1039/C29690000526

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