Issue 7, 1983

Intramolecular [2 + 2] photocycloadditions of E and Z olefins to cyclohex-2-enone

Abstract

The [2 + 2] intramolecular photocycloaddition of E and Z olefins to a cyclohexenone has been investigated; it is concluded that the bond to C(3) in the cyclohexenone is formed first to give the diradical intermediates (7a) and (7b).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 371-373

Intramolecular [2 + 2] photocycloadditions of E and Z olefins to cyclohex-2-enone

D. Becker, M. Nagler, S. Hirsh and J. Ramun, J. Chem. Soc., Chem. Commun., 1983, 371 DOI: 10.1039/C39830000371

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