C–H/N–H cross-coupling has become a key technology for the selective conjugation of azole drugmolecules. However, the development of new synthetic models and green chemical methods is imperative to enhance the construction of multi-functional compounds and compounds with unique functional groups. We herein reported an electrochemical synthesis of α-tetrazolyl ketones with excellent yields and broad
Design, synthesis, in vitro antimicrobial and cytotoxic evaluation of novel 1,2,3-selena/thiadiazolyltetrazole derivatives
作者:S. Kanakaraju、L. Suresh
DOI:10.1039/c4ra12670j
日期:——
A new series of 2,5-disubstituted tetrazoles and 1,2,3-selena/thiadiazolyl-2H-tetrazole derivatives were synthesized and evaluated for theirin vitroantimicrobial and cytotoxic activities against pathogenic strains.