72721-56-3Relevant academic research and scientific papers
[Omim][Bf4] ionic liquid, a green and recyclable medium for one-pot aminomethylation of electron-rich aromatic compounds
Arzephoni, Amene Yaghoubi,Naimi-Jamal, M. Reza,Sharifi, Ali,Abaee, M. Saeed,Mirzaei, Mojtaba
, p. 216 - 218 (2013/07/05)
An efficient catalyst-free procedure has been developed for one-pot aminomethylation of some electron-rich aromatic compounds such as 1- and 2-naphthols, indole, N-methylindol and benzamide, in [omim][BF4] ionic liquid at room temperature. The ionic liquid can be recovered and reused without any noticeable loss of performance.
Peroxo complexes of uranium(VI) containing nitrogen and oxygen donor ligands1
Singh, Balgar,Mahajan, Simpy,Sheikh,Sharma, Mohita,Kalsotra, Bansi Lal
body text, p. 1079 - 1088 (2012/10/08)
The uranium(VI) peroxo complexes containing Mannich base ligands having composition [UO(O2)L-L(NO3)2] {where L-L = morpholinobenzyl acetamide (MBA), piperidinobenzyl acetamide (PBA), morpholinobenzyl benzamide (MBB), piper
Solvent-free preparation of monoacylaminals assisted by microwave irradiation
Sharifi,Mohsenzadeh,Naimi-Jamal
, p. 394 - 396 (2007/10/03)
Reaction of amide 1, aldehyde 2, and amine 3 promoted by microwave irradiation produced monoacylaminals 4 up to 100% yield in a short time under solvent-free conditions.
Monoacylaminals by the benzotriazole-assisted aminoalkylation of amides
Katritzky, Alan R.,Fali, Clara N.,Bao, Weiliang,Qi, Ming
, p. 1421 - 1423 (2007/10/03)
A general synthesis of a range of monoacylaminals from the reaction of N-(α-aminoalkyl)benzotriazoles with amides in the presence of a base has been developed. In less reactive cases zinc bromide was used to facilitate the above reaction.
