Facile synthesis of 3-aryl/alkylamino 5-aryl/alkyl 1, 2, 4-oxadiazoles from acylthiourea
G Chennakrishnareddy, H Debasis, R Jayan…
Index: Chennakrishnareddy, Gundala; Debasis, Hazra; Jayan, Rapai; Manjunatha, Sulur G. Tetrahedron Letters, 2011 , vol. 52, # 46 p. 6170 - 6173
Full Text: HTML
Citation Number: 8
Abstract
Facile and selective synthesis of 3-aryl/alkylamino 5-aryl/alkyl 1, 2, 4-oxadiazoles starting from N-acylthioureas has been demonstrated. The regio-selectivity is achieved by simply selecting an appropriate base used for the generation of hydroxyl amine from the corresponding hydrochloride salt. This method also avoids the use of toxic cyanogen bromide. The structure of the synthesized oxadiazoles has been resolved by tandem mass ...
Related Articles:
[Souldozi, Ali; Ramazani, Ali; Dadrass, Ali Reza; Slepokura, Katarzyna; Lis, Tadeusz Helvetica Chimica Acta, 2012 , vol. 95, # 2 p. 339 - 348]
[Chan, Chung Woo; Ng, Chun Ming Dominic; Ho, Joyce; Tin, Kam Chung Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1997 , vol. 36, # 3 p. 216 - 219]
[Uher, Michal; Foltin, Jozef; Floch, Lubomir Collection of Czechoslovak Chemical Communications, 1981 , vol. 46, # 11 p. 2696 - 2702]
[Uher, Michal; Foltin, Jozef; Floch, Lubomir Collection of Czechoslovak Chemical Communications, 1981 , vol. 46, # 11 p. 2696 - 2702]