Cyclization of Semicarbazones to 1,2,3-Selenadiazoles By Selenium Dioxide

Section: Article
Published
Jun 1, 2012
Pages
21-25

Abstract

Abstract In the present work some of 1,2,3-selenadiazole compounds derived from corresponding semicabazones have been prepared. The reaction of substituted chalcone compounds (1a-c) and 4-methoxy benzyl cyanide give compounds (2a-c) which were converted through the reaction with semicarbazide hydrochloride into the corresponding semicarbazones (3a-d(. The treatment of these compounds with selenium dioxide leads to ring closure of semicarbazones to give the 1,2,3-selenadiazole compounds. The structures of the synthesized compounds were established by physical and spectral methods.

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How to Cite

[1]
O. Th. Ali Al-Obaidy and عمر, “Cyclization of Semicarbazones to 1,2,3-Selenadiazoles By Selenium Dioxide”, EDUSJ, vol. 25, no. 2, pp. 21–25, Jun. 2012.