35314-01-3Relevant academic research and scientific papers
FeCl3-promoted synthesis of 1,3,4-thiadiazoles under combined microwave and ultrasound irradiation in water
Feng, Huangdi,Ying, Xili,Peng, Yanqing,Van Der Eycken, Erik V.,Liu, Chuanduo,Zhao, Shanshan,Song, Gonghua
, p. 681 - 686 (2013/07/26)
An eco-friendly and efficient synthesis of substituted 1,3,4-thiadiazole derivatives has been developed. This aqueous heterogeneous approach proceeds smoothly and quickly under combined microwave and ultrasound irradiation in the presence of FeCl3.
One-pot synthesis and anticancer studies of 2-arylamino-5-aryl-1,3,4- thiadiazoles
Kumar, Dalip,Vaddula, Buchi Reddy,Chang, Kuei-Hua,Shah, Kavita
experimental part, p. 2320 - 2323 (2011/05/15)
A series of 2-arylamino-5-aryl-1,3,4-thiadiazoles 1a-j were synthesized and screened for their anticancer activity against various human cancer cell lines. The novel one-pot synthesis of 1,3,4-thiadiazoles was achieved by refluxing aryl aldehydes, hydrazi
1,3,4-Thiadiazoles. Regioselective O-demethylation on dehydrative cyclization of 1-(3,4,5-trimethoxybenzoyl)-4-substituted thiosemicarbazides with sulphuric acid
Al-Omar, Mohamed,Al-Deeb, Omar A.,Al-Khamees, Hamad A.,El-Emam, Ali A.
, p. 2509 - 2517 (2007/10/03)
Cyclization of 1-(3,4,5-trimethoxybenzoyl)-4-substituted thiosemicarbazides 2a-g with sulphuric acid at ambient temperature afforded the selectively demethylated products 2-(4-hydroxy-3,5-dimethoxyphenyl)-5-substituted amino-1,3,4-thiadiazoles 4a-g. Meanw
