Synthesis and Antitubercular Activity of 2, 3-Disubstituted-5-[ω-Carboxyheptyl]-4-Thioazolidinoes
Corresponding Author(s) : Anjani Solankee
Asian Journal of Chemistry,
Vol. 6 No. 3 (1994): Vol 6 Issue 3
Abstract
2, 3-Disubstituted-4-thiazolidinones have been synthesized by refluxing Schiff bases with 2-mercaptosebacic acid using benzene as solvent. The compounds have been screened for their antitubercular activity against H37Rv strain of Mycobacterium tuberculosis.
Keywords
synthesis
Antitubercular Activity
2, 3-Disubstituted-5-[ω-Carboxyheptyl]-4-Thioazolidinoes
Solankee, A., & Kapadia, K. (2010). Synthesis and Antitubercular Activity of 2, 3-Disubstituted-5-[ω-Carboxyheptyl]-4-Thioazolidinoes . Asian Journal of Chemistry, 6(3), 713–714. Retrieved from https://asianpubs.org/index.php/ajchem/article/view/24641
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