113643-84-8Relevant articles and documents
Facile synthesis and stracture of novel 2,5-disubstituted 1,3,4-selenadiazoles
Hua, Guoxiong,Li, Yang,Fuller, Amy L.,Slawin, Alexandra M.Z.,Woollins, J. Derek
experimental part, p. 1612 - 1618 (2009/08/09)
The reaction of hydrazide with carbony] chloride in the presence of sodium carbonates leads to the corresponding 1,2- diacylhydrazines [1a-t, R 1C(O)NHNHC(O)R2, R1 = aryl, R2 = aryl or alkyl] in moderate to excellent yield (57-90%). The latter reacts with 2,4-diphenyl-l,3-diselenadiphosphetane- 2,4-diselenide (Woollins' reagent, WR) in refluxing toluene to give a series of new 2,5-disubstituted 1,3,4-selenadiazoles (2a-t, 51-99% yield). All compounds were characterized spectroscopically and six compounds were characterized crystalloqraphically. Wiley-VCH Verlag GmbH & Co. KGaA.
Facile synthesis of symmetric and unsymmetric 1,3,4-oxadiazoles using 2-acyl(or aroyl)pyridazin-3-ones
Park, Yong-Dae,Kim, Jeum-Jong,Chung, Hyun-A,Kweon, Deok-Heon,Cho, Su-Dong,Lee, Sang-Gyeong,Yoon, Yong-Jin
, p. 560 - 564 (2007/10/03)
Symmetric and unsymmetric 1,3,4-oxadiazoles were synthesized in situ from hydrazine hydrate and the corresponding 2-acyl-4,5-dichloropyridazin-3-ones as acylating agents in polyphosphoric acid or BF3·OEt2 in excellent yields.