23275-54-9Relevant academic research and scientific papers
A diversified assembly of 1,2,4-oxadiazol-3-amines: Metallic thiophile catalyzed chemoselective one-pot reaction of aryl isothiocyanates, amidines/guanidines, and hydroxylamine
Jalani, Hitesh B.,Sudarsanam, V.,Vasu, Kamala K.
, p. 3378 - 3386,9 (2012/12/12)
An efficient one-pot synthesis of 1,2,4-oxadiazol-3-amines from simple starting materials, isothiocyanates, amidines/guanidines, and hydroxylamine, is described. The reaction is facilitated by metallic-thiophile-assisted desulfurization of in situ formed amidino- or guanidinothiourea to give chemoselectively N-hydroxyguanidine intermediates that give exclusively various 1,2,4-oxadiazol-3-amines in good to excellent yields. The reaction mechanistic pathway may proceed through an intramolecular 5-exo-trig cyclization.
Photochemical Behaviour of Some 1,2,4-Oxadiazole Derivatives
Buscemi, Silvestre,Cicero, Maria G.,Vivona, Nicolo,Caronna, Tullio
, p. 1313 - 1316 (2007/10/02)
The photochemical behaviour of some 1,2,4-oxadiazole derivatives in methanol has been studied at 254 nm.On irradiation, 3-amino- (or 3-methylamino-) 5-aryl-1,2,4-oxadiazoles underwent a ring photoisomerization to 1,3,4-oxadiazoles, probably through a 'rin
