Design, synthesis and antibacterial activity of novel 1,3-thiazolidine pyrimidine nucleoside analogues

Sriharsha, S. N. and Satish, S. and Shashikanth, S. and Raveesha, K. A. (2006) Design, synthesis and antibacterial activity of novel 1,3-thiazolidine pyrimidine nucleoside analogues. BIOORGANIC & MEDICINAL CHEMISTRY, 14 (22). pp. 7476-7481.

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Official URL: http://dx.doi.org/10.1016/j.lfs.2006.08.032

Abstract

The synthesis of a new class of 1, 3-thiazolidine nucleoside analogues in which furanose oxygen atom was replaced with nitrogen atom and T-carbon atom with sulfur atom is described. N-tert-butoxycarbonyl-2-acyloxy-4-trityloxymethyl-1,3-thiazolidine was coupled with the pyrimidine bases like uracil, thymine, etc. in the presence of lewis acids stannic chloride or trimethyl silyl triflate following Vorbruggen procedure. The antibacterial activity of the novel 1,3-thiazolidine pyrimidine nucleoside analogues is highlighted. All compounds (7a-e) with free NH group in the pyrimidine moiety showed significant biological activity against all the standard strains used and in that compounds 7d and 7e showed significant activity against 14 human pathogens tested. (c) 2006 Elsevier Ltd. All rights reserved.

Item Type: Article
Uncontrolled Keywords: 1,3-thiazolidine nucleosides; Vorbruggen coupling; NOE experiment; antibacterial activity
Subjects: Agriculture Biological Sciences > Microbiology
University of Mysore > PG Campuses > Manasagangotri, Mysore > Agriculture Biological Sciences > Microbiology

Physical Sciences > Chemistry
Divisions: PG Campuses > Manasagangotri, Mysore > Microbiology
Depositing User: Users 17 not found.
Date Deposited: 26 Apr 2013 11:54
Last Modified: 02 Sep 2013 05:30
URI: http://eprints.uni-mysore.ac.in/id/eprint/5039

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