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Thiazolidinones: Synthesis and Antitubercular Activity of 2,3-Disubstituted -5- (W - Carboxy, Heptyl) -4-Thiazolidinones (Part II)

Volume 10, Number 1

Anjani Solankee* And Kishor Kapadia

Chemistry Department, B.K.M. Science College, Valsad - 396001 India.

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ABSTRACT:

Several -2- phenyl -3- substituted phenyl/naphthyl -5- (W - carboxy heptyl) -4- thiazolidinones have been prepared by condensing schiff bases, from arylamines and benzaldehyde, with 2 - mercapto sebacic acid. The title compounds were screened for antitubercular activity. The structure has been studied by elemental and spectral analysis.

KEYWORDS:

Thiazolidinones; 3-Disubstituted; Elemental

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Solankee a, Kapadia K. Thiazolidinones: Synthesis and Antitubercular Activity of 2,3-Disubstituted -5- (W - Carboxy, Heptyl) -4-Thiazolidinones (Part II). Orient J Chem 1994;10(1).

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Solankee a, Kapadia K. Thiazolidinones: Synthesis and Antitubercular Activity of 2,3-Disubstituted -5- (W - Carboxy, Heptyl) -4-Thiazolidinones (Part II). Orient J Chem 1994;10(1). Available from:http://www.orientjchem.org/?p=38217

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