1236827-22-7Relevant articles and documents
A convenient strategy for the synthesis of 3,5-diaryl-1,2,4-thiadiazoles: Oxidative dimerization of arylthioamides using CC-DMSO in PEG-400
Khosropour, Ahmad Reza,Noei, Jalil
, p. 649 - 651 (2010)
An inexpensive and effective preparative protocol for the highly efficient synthesis of structurally diverse 3,5-diaryl-1,2,4-thiadiazoles at ambient temperature with 2,4,6-trichloro-1,3,5-triazine (CC) and DMSO in polyethylene glycol 400 (PEG-400) as sol
Highly efficient synthesis of 3,5-diaryl-1,2,4-thiadiazoles in water-wet paste conditions
Boeini, Zali Hassan
, p. 2932 - 2938 (2011)
1,3-Dibromo-5,5-diphenylimidazolidine-2,4-dione (N,N'-dibromo phenytoin) was efficiently used for the rapid conversion of thiobenzamides to the corresponding 3,5-diaryl-1,2,4-thiadiazoles in water-wet paste conditions. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications to view the free supplemental file. Taylor & Francis Group, LLC.
Copper(II)-mediated homocoupling of thioamides for the synthesis of 1,2,4-thiadiazoles
Sun, Yadong,Wu, Wanqing,Jiang, Huanfeng
, p. 4239 - 4243 (2014/07/21)
A copper(II)-mediated highly selective oxidative cyclization reaction of thioamides to provide 3,5-disubstituted 1,2,4-thiadiazoles was developed. The copper species plays a key role in this transformation and different functional groups are tolerated under the optimal reaction conditions. Copyright