Synthesis and antimicrobial activity of α N-Phthilimido and acetimido derivatives from amino acids and Anhydrides

Reddy, C. Uma Maheswara (37095986500) and Jayakar, Balasundaram (6603630993) and Srinivasan, R. (58797312300) (2010) Synthesis and antimicrobial activity of α N-Phthilimido and acetimido derivatives from amino acids and Anhydrides.

Full text not available from this repository.

Abstract

The phthaloyl and acetyl group are common protecting groups from are common protecting group for amines in organic synthesis 1 and are also important pharmacophores 2. Common method are imide synthesis include dehydrative condensation of an anhydride and amino acid at high temperature, the acid-catalyzed cyclization of N-substituted amic acid. Abdol Reza Hajipour 3, rapidly synthesised Phthalimide derivatives by microwave irradiation. A simple extremely fast, and high yielding method for the reaction of phthalic anhydride with a number of amino acids using microwave irradiation under solventless dry condition has been developed. The aim of the study was to design, synthesize and investigate the antimicrobial and antifungal activities, anticancer activities of some α N-Phthilimido and acetylated derivatives of amino acids. The chemical structures of the titled compound were confirmed by IR, 13CNMR and elemental analysis. All the compounds were screened for antimicrobial activity against gram positive, gram negative bacteria (Escherichia coli, Klebsiella, Staphylococcus epidermitis, Bacillus cereus, Micrococcus leteus, Staphylococcus aureus) and fungal strains (Candida albicans, Aspergillus niger). © 2012 Elsevier B.V., All rights reserved.

Item Type: Article
Subjects: Medicine > Pharmacology
Divisions: Pharmacy > Vinayaka Mission's College of Pharmacy, Salem > Pharmacy
Depositing User: Unnamed user with email techsupport@mosys.org
Last Modified: 11 Dec 2025 06:17
URI: https://vmuir.mosys.org/id/eprint/5148

Actions (login required)

View Item
View Item