1443438-82-1Relevant articles and documents
The reaction of N -isocyaniminotriphenylphosphorane with biacetyl in the presence of (E) -cinnamic acids: Synthesis of fully substituted 1,3,4-oxadiazole derivatives via intramolecular aza -wittig reactions of in situ generated iminophosphoranes
Ramazani, Ali,Abdian, Behnaz,Nasrabadi, Fatemeh Zeinali,Rouhani, Morteza
, p. 642 - 648 (2013)
Reaction of N-isocyaniminotriphenylphosphorane with biacetyl in the presence of (E)-cinnamic acids proceeds smoothly at room temperature and under neutral conditions to afford sterically congested 1,3,4-oxadiazole derivatives in high yields. The reaction
Ultrasound-Promoted Three-Component Reaction of N -isocyaniminotriphenyl-phosphorane, (E)-cinnamic Acids, and Biacetyl
Ramazani, Ali,Rouhani, Morteza,Zeinali Nasrabadi, Fatemeh,Gouranlou, Farideh
supporting information, p. 20 - 28 (2015/10/29)
Fully substituted 1,3,4-oxadiazole derivatives were obtained in a one-pot three-component reaction of N-isocyaniminotriphenylphosphorane, biacetyl, and (E)-cinnamic acids in dichloromethane under ultrasound irradiation. This rapid method produced the products in short reaction times (16-27 min) and excellent yields (91-97%). GRAPHICAL ABSTRACT.