Issue 11, 1989

Photochemical reactivity of imines from benzil mono-oxime esters

Abstract

The synthesis and photochemical reactions of some 1,4-diaza-1,3-dienes have been studied. The photochemical reactivity of these compounds falls into two distinct types. Thus the diazadienes (7ad) undergo hydrogen abstraction and cyclisation to 2H-imidazoles while diazadiene (7e) cyclises by either of two six-electron paths to yield either phenanthridine or quinoxaline derivatives.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1989, 2035-2038

Photochemical reactivity of imines from benzil mono-oxime esters

D. Armesto, W. M. Horspool, M. Apoita, M. G. Gallego and A. Ramos, J. Chem. Soc., Perkin Trans. 1, 1989, 2035 DOI: 10.1039/P19890002035

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