A convenient synthesis of substituted piperazines via aminomercuration??demercuration of diallylamines
J Barluenga, C Najera, M Yus
Index: Barluenga, J.; Najera, C.; Yus, M. Journal of Heterocyclic Chemistry, 1980 , vol. 17, p. 917 - 921
Full Text: HTML
Citation Number: 10
Abstract
Abstract cis and trans-2, 6-Bis [bromomercuriomethyl] piperazines II which bear equal or different substituents at each nitrogen are obtained in the reaction of N-substituted diallylamines with mercury (II) acetate and aryl-amines followed by a double decomposition process with potassium bromide. Their reduction with sodium borohydride lead to the corresponding 1, 4-disubstituted cis-and trans-2, 6-dimethylpiperazines III. Steric factors ...
Related Articles:
Synthesis of high-molecular-weight polyamine by radical polymerization ofN, N-diallyl-N-methylamine
[Vasilieva; Kleshcheva; Gromova; Rebrov; Filatova; Krut'ko; Timofeeva; Topchiev Russian Chemical Bulletin, 2000 , vol. 49, # 3 p. 431 - 437]
[Journal of Organic Chemistry, , vol. 31, p. 1975 - 1977]