79946-46-6Relevant academic research and scientific papers
Efficient microwave-assisted synthesis and antioxidant activity of 4-arylidene-2-phenyl-1H-imidazol-5(4H)-ones
Shi, Feng,Zeng, Xiao-Ning,Wu, Fei-Yue,Yan, Shu,Zheng, Wei-Fa,Tu, Shu-Jiang
experimental part, p. 59 - 63 (2012/04/23)
The efficient synthesis of 4-arylidene-2-phenyl-1H-imidazol-5(4H)-ones was achieved via microwaveassisted reactions of 4-arylmethylene-2-phenyloxazol-5(4H) -ones with urea in glycol. This approach provides a facile shortcut for the synthesis of this type
A practical and efficient synthesis of 2,5-disubstituted-3,5-dihydro- imidazol-4-ones from oxazolones
Chavez, Flavio,Pavy, Caslin,Williamson, Thomas,Cleary, Thomas
, p. 3321 - 3327 (2012/09/21)
An alternative procedure for the synthesis of 2,5-disubstituted-3,5- dihydro-imidazol-4-ones from substituted oxazolones was evaluated. The initial oxazolone ring-opening reaction was examined with a variety of ammonia source compounds followed by the sub
Condensation of unsaturated azlactones with urea and thiourea: Some observations
Mukerjee, Arya K.,Joseph, Kiran,Homami, Sayed Saied,Sanjayan, Gangadhar J.
, p. 973 - 974 (2007/10/02)
4-Arylmethyleneoxazol-5-ones (1c,d) on condensation with urea/thiourea form the corresponding imidazol-5-ones (4c,d), whereas 4-cyclohexylideneoxazol-5-one (1e) gives 2-cyclohexylideneacetamido (5).A plausible mechanism has been discussed.
