143883-15-2Relevant academic research and scientific papers
Convenient preparation of unsymmetrical 2,5-disubstituted 1,3,4-oxadiazoles promoted by Dess-Martin reagent
Dobrotǎ, Cristian,Paraschivescu, Codru?a C.,Dumitru, Ioana,Matache, Mihaela,Baciu, Ion,Ru?ǎ, Lavinia L.
scheme or table, p. 1886 - 1888 (2009/07/05)
2,5-Disubstituted 1,3,4-oxadiazoles have been conveniently prepared by oxidative cyclization of N-acyl-N′-aryliden-hydrazines promoted by an excess of Dess-Martin periodinane under mild conditions (23 examples, up to 92% isolated yields).
Triethyl phosphite mediated synthesis of indazoloquinazolinoperimidines, oxadiazoloindazoles and thiadiazoloindazoles
Reddy, V Rama Kishan,Reddy, P S N,Ratnam, C V
, p. 499 - 502 (2007/10/02)
2-(2-Aminophenyl)perimidine (1) on treatment with 2-nitrobenzaldehydes (2) in acetic acid gives 5,6-dihydro-6-(2-nitroaryl)quinazolinoperimidines (4) which on permanganate oxidation yield 6-(2-nitroaryl)quinazolinoperimidines (5). 5-on triethylphosphite (TEP) mediated deoxygenative cyclisation afford indazoloquinazolinoperimidines (6).Similarly, 5-aryl-2-(2-nitrophenyl)oxadiazoles (9) and 2-arylamino-5-(2-nitrophenyl)thiadiazoles (14) on treatment with TEP give 2-aryloxadiazoloindazoles (10) and2-(N-ethylarylamino)thiadiazoloindazoles (16) respectively.
