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 (7a–d) 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.