Tetrazoles: LIII. Microwave-activated acylation of 5-substituted tetrazoles
YA Efimova, TV Artamonova, GI Koldobskii
Index: Efimova; Artamonova; Koldobskii Russian Journal of Organic Chemistry, 2008 , vol. 44, # 9 p. 1345 - 1347
Full Text: HTML
Citation Number: 16
Abstract
Abstract The acylation of 5-aryl (hetaryl) tetrazoles with acetic and benzoic anhydrides under microwave irradiation gave the corresponding 2-substituted 5-methyl-and 5-phenyl-1, 3, 4- oxadiazoles in high yields. The use of microwave activation reduces the reaction temperature by 30–40° C and shortens the reaction time by a factor of 5 to 7.
Related Articles:
[Conole, Daniel; Beck, Thorsten M.; Jay-Smith, Morgan; Tingle, Malcolm D.; Eason, Charles T.; Brimble, Margaret A.; Rennison, David Bioorganic and Medicinal Chemistry, 2014 , vol. 22, # 7 p. 2220 - 2235]
[Mashraqui, Sabir H.; Ghadigaonkar, Shailesh G.; Kenny, Rajesh S. Synthetic Communications, 2003 , vol. 33, # 14 p. 2541 - 2545]
[Huisgen,R. et al. Chemische Berichte, 1960 , vol. 93, p. 2106 - 2124]
[Li, Qiang; Tao, Yi; Xu, Dongfang; Zhang, Haobing; Duan, Liping Journal of the Chinese Chemical Society, 2014 , vol. 61, # 6 p. 665 - 670]
[Peet, Norton P.; Sunder, Shyam Journal of Heterocyclic Chemistry, 1984 , vol. 21, p. 1807 - 1816]