External vs. internal cyclopropyl bond cleavage in the photosensitized epimerization of bicyclo[3,1,0]hex-2-enes
- 1 January 1972
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Chemical Communications
- No. 1,p. 33-34
- https://doi.org/10.1039/c39720000033
Abstract
The photosensitized epimerizations of bicyclo-[3,1,0]hex-2-ene-6-endo-carboxylic acid and its methyl ester occur exclusively by cleavage of the external cyclopropyl bond.Keywords
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