Abstract
A reliable synthetic method has been developed for 2, 4, 5-trisubstituted imidazole from benzil, ammonium acetate, and aromatic aldehyde by using papain a non toxic and inexpensive catalyst. The Structural features have been arrived at from their analytical data, IR, Mass, 1H NMR. The antibacterial activity of all synthesized compound has been performed by using filter paper disc method against gram positive and gram negative bacteria.We observed that 4a –compound is more active against gram +ve S. Typhi at lower concentration 4f less active against gram +ve S. Typhi and gram –ve E. Coli
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callMore From: Asian Journal of Biomedical and Pharmaceutical Sciences
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
