The preparation and lead tetraacetate oxidation of mixed bisaroyl hydrazones of biacetyl to l-(alpha-aroyloxyarylideneamino)-3,5-dimethyl-1,2,3-triazoles
Cp. Hadjiantoniou-maroulis, The preparation and lead tetraacetate oxidation of mixed bisaroyl hydrazones of biacetyl to l-(alpha-aroyloxyarylideneamino)-3,5-dimethyl-1,2,3-triazoles, HETEROCYCLE, 51(3), 1999, pp. 599-604
The preparation and lead tetraacetate oxidation of the mixed aroyl hydrazon
es of biacetyl (2) to the pairs of isomeric 1-(alpha-aroyloxyarylideneamino
)-3,5-dimethyl-1,2,3-triazoles (6) and (6') is described. The product ratio
of 6/6' is evaluated in terms of the stability imparted to the zwiterionic
intermediate (5) by the different substituents on the aroyl groups.