Abstract
A series of Compound 4‐(2᾽‐hydroxy‐3᾽‐chloro‐5᾽‐ethyl phen‐1᾽‐yl)‐1‐(4᾽‐tolyl)‐3‐chloro‐2‐azetidinone 4a‐j have been prepared by the reaction of 2 ‐hydroxy‐3 ‐chloro‐5 ‐ethyl‐N‐(p‐tolyl)‐chalconimines 3a‐j with chloroacetyl chloride in the presence of triethylamine. The Schiff base derivatives 3a‐j has been prepared by the condensation of different substituted chalone derivatives 1 with p‐toluidine 2. The synthesized compounds were screened for their antibacterial activity against Staphylococcus aureus and Escherichia 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 callDisclaimer: 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.
