Cyclohexadienones: stereospecific photochemical rearrangements of o-quinol acetates
- 1 January 1969
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society D: Chemical Communications
- No. 10,p. 526-527
- https://doi.org/10.1039/c29690000526
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.Keywords
This publication has 0 references indexed in Scilit: