Abstract 1-Phenylmethyl-and 1-(4-methoxyphenylmethyl)-5-chloro-1, 2, 3-triazole-4- carbonyl chlorides acylated the pyrrolidine enamines of cyclopentanone and cyclohexanone, and the resulting enaminones underwent transaminations with aryl amines under acidic conditions. The products then cyclized under basic conditions to linearly fused, tricyclic 3-phenylmethyl-and 3-(4-methoxyphenylmethyl)-4-aryl-8-oxo-4, 5, 6, 7- ...
[Cottrell, Ian F.; Hands, David; Houghton, Peter G.; Humphrey, Guy R.; Wright, Stanley H. B. Journal of Heterocyclic Chemistry, 1991 , vol. 28, # 2 p. 301 - 304]
