Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Australian Journal of Chemistry Australian Journal of Chemistry Society
An international journal for chemical science
RESEARCH ARTICLE

Pyrazine chemistry. II. Reduction of 3,6-Dibenzylidenepiperazine-2,5-diones

SM Marcuccio and JA Elix

Australian Journal of Chemistry 37(8) 1791 - 1794
Published: 1984

Abstract

A reinvestigation of the reduction of 3,6-dibenzylidenepiperazine-2,5-dione (1) with zinc and acetic acid established that this reaction gave (Z)-6-benzyl-3-benzylidenepiperazine-2,5-dione (10). When a mixture of acetic acid and hydrochloric acid was used in the reduction, a mixture of trans- (12) and cis-3,6-dibenzylpiperazine-2,5-dione (5) was obtained. Direct catalytic reduction of 3,6-di(2-chloro- benzy1idene)piperazine-2,5-dione (2) to (±)-cis-3,6-di(2-chlorobenzyl)piperazine-2,5-dione (6) was also accomplished.

https://doi.org/10.1071/CH9841791

© CSIRO 1984

Committee on Publication Ethics


Export Citation Get Permission

View Dimensions

View Altmetrics