TY - JOUR
T1 - Synthesis, characterization and antimicrobial activity of some novel 2,3-disubstituted thiazolidin-4-one derivatives
AU - Chandrashekhar Kumar, B.
AU - Venugopala Reddy, K. R.
AU - Fasiulla, null
AU - Shridhara, A. M.
PY - 2013/8/1
Y1 - 2013/8/1
N2 - A series of new 3-(4-(p-toluidino)thiazol-2-yl)-2-phenylthiazolidin-4-one derivatives (5a-g) were synthesized from novel schiff base of 2-((4-(p-toluidino)thiazol-2-ylimino)methyl)phenol (4a-g) with thioglycolic acid in presence of anhydrous zinc chloride. The chemical structures of these compounds were confirmed by various physic-chemical methods viz, IR, 1H NMR, mass spectral data and elemental analysis. Newly synthesized compounds were screened in vitro for their antimicrobial activity against varieties of gram +ve and gram -ve bacterial strains such as Bacillus subtilis, Pseudomonas aeruginosa and fungi strain Candida albicans & Aspergillus nigar at 40 μg/mL. The chloro and bromo substituted 2,3-substituted thiazolidin-4-one derivatives are showing activity as compare to the other functional groups.
AB - A series of new 3-(4-(p-toluidino)thiazol-2-yl)-2-phenylthiazolidin-4-one derivatives (5a-g) were synthesized from novel schiff base of 2-((4-(p-toluidino)thiazol-2-ylimino)methyl)phenol (4a-g) with thioglycolic acid in presence of anhydrous zinc chloride. The chemical structures of these compounds were confirmed by various physic-chemical methods viz, IR, 1H NMR, mass spectral data and elemental analysis. Newly synthesized compounds were screened in vitro for their antimicrobial activity against varieties of gram +ve and gram -ve bacterial strains such as Bacillus subtilis, Pseudomonas aeruginosa and fungi strain Candida albicans & Aspergillus nigar at 40 μg/mL. The chloro and bromo substituted 2,3-substituted thiazolidin-4-one derivatives are showing activity as compare to the other functional groups.
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M3 - Article
AN - SCOPUS:84880709145
VL - 5
SP - 1
EP - 6
JO - Journal of Chemical and Pharmaceutical Research
JF - Journal of Chemical and Pharmaceutical Research
IS - 6
ER -