442160-82-9Relevant academic research and scientific papers
Structure-cytotoxicity relationship of a novel series of miconazole-like compounds
Yousefi, Reza,Khalafi-Nezhad, Ali,Panahi, Farhad,Soltani Rad, Mohammad Navid,Behrouz, Somayeh,Esmaili, Mansoore,Ghaffari, Sayed Mahmoud,Moosavi-Movahedi, Ali Akbar,Niazi, Ali
, p. 1921 - 1928,8 (2020/07/30)
In the current study, two novel classes of the carboacyclic nucleosides having miconazole-like scaffolds as imidazole- and pyrimidine-based compounds were examined for their cytotoxic properties. The aim was to establish a relation between cytotoxic activ
Studies with 1-functionally substituted alkyl azoles: Novel synthesis of functionally substituted azolylbenzimidazoles and functionally substituted azolyl-1,2,4-triazoles
Abdel-Megid, Mohamed,Elnagdi, Mohamed H.,Negm, Abdalla M.
, p. 105 - 108 (2007/10/03)
ω-Azolylacetophenones 1 and 2 react with dimethylformamide dimethylacetal to yield enaminones 7,8 that were converted into azolylazoles via reaction with hydrazine and with hydroxylamine. Compounds 1,2 also coupled with aromatic diazonium salts to yield arylhydrazones and reacted with nitrous acid to yield corresponding oximes.
