73014-97-8Relevant academic research and scientific papers
Unprecedented conversion of (Z)-3-chloro-3-arylacrylic acids to benzoic acids: Synthesis of s-triazolo[3,4-b][1,3,4]thiadiazoles
Sahi, Seema,Bhardwaj, Madhvi,Paul, Satya
supporting information, p. 3809 - 3812 (2014/07/07)
An unprecedented method for the conversion of (Z)-3-chloro-3-arylacrylic acids to corresponding benzoic acids by stirring in POCl3 at 80 °C is reported. The benzoic acids formed in situ undergo condensation with 4-amino-5-aryl-3-mercapto-1,2,4-
Anodic formation of 3,6-diaryl-[1,2,4]triazolo[3,4-b][1,3,4]thiadiazoles and 2(3-aryl-5-methyl-1H-[1,2,4]triazol-1-yl)-5-aryl-1,3,4-thiadiazoles
Batanero, Belen,Saez, Rebeca,Barba, Fructuoso
experimental part, p. 3076 - 3080 (2011/05/19)
3,6-Disubstituted 1,2,4-triazolo[3,4-b][1,3,4]thiadiazoles together with the unknown systems 2-(3-aryl-5-methyl-1H-[1,2,4]triazol-1-yl)-5-aryl-1,3,4- thiadiazoles were obtained by anodic oxidation, under aprotic conditions, of aryl aldehyde N-(5-aryl-1,3,
Silica-supported dichlorophosphate as a recoverable cyclodehydrant: Expeditious synthesis of [1,2,4]triazolo[3,4-b][1,3,4]thiadiazoles under microwave irradiation
Li, Zheng,Zhao, Yanlong
experimental part, p. 3816 - 3824 (2009/12/08)
An expeditious novel approach to 3,6-disubstituted [1,2,4]triazolo[3,4-b] [1,3,4]thiadiazoles using silica-supported dichlorophosphate as a recoverable cyclodehydrant, carboxylic acids and thiocarbohydrazide as starting materials, and microwave irradiatio
