Issue 15, 1987

Photochemical deazetation of 2,3-diazabicyclo[2.2.2]oct-2-ene; unexpected inversion of stereochemistry

Abstract

Irradiation of cis-anti-[5,6-2H2]-2,3-diazabicyclo[2.2.2]oct-2-ene leads to bicyclo[2.2.0]hexane in which the deuterium is predominantly exo, i.e., with inversion of configuration, and hexa-1,6-diene in which the 1,6-positions show equal amounts of cis and trans deuterium; the inversion is explained in terms of one-bond cleavage and conformational changes in a diazenyl biradical.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 1179-1181

Photochemical deazetation of 2,3-diazabicyclo[2.2.2]oct-2-ene; unexpected inversion of stereochemistry

A. J. F. Edmunds and C. J. Samuel, J. Chem. Soc., Chem. Commun., 1987, 1179 DOI: 10.1039/C39870001179

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