Transaminations of enaminones: A Synthesis of tricyclic, N??aryl, 1, 2, 3??triazole??fused pyridones

…, R Friary, H Jones, JH Schwerdt, V Seidl…

Index: Chan, Tze-Ming; Friary, R.; Jones, H.; Schwerdt, J. H.; Seidl, V.; et al. Journal of Heterocyclic Chemistry, 1990 , vol. 27, # 4 p. 1135 - 1142

Full Text: HTML

Citation Number: 5

Abstract

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- ...

Related Articles:

An improved procedure for the preparation of 1??benzyl??1H??1, 2, 3??triazoles from benzyl azides

[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]

More Articles...