Knoevenagel condensation of various aromatic aldehydes with 2,4-thiazolidinedione has been carried out in polyethylene glycol-300. The reactions were carried out at moderate temperature with very simple isolation procedure and with better yields.
Synthesis and Microbial Activity of New Thiazolyl-1,4-benzothiazines. -Some new thiazolyl-1,4-benzothiazines (VI) are synthesized via oxidative cyclocondensation of diones (IV) with 2-aminobenzenethiol (V) and evaluated for their antibacterial and antifungal activity in vitro. -(DENGLE, R. V.; INGLE, R. D.; BONDGE, S. P.; MANE, R. A.; Indian J. Chem., Sect. B: Org.
Thiazole derivatives R 0260 Rapid and Convenient Synthetic Strategy for 2-Amino-4-aryl-5-aryl-sulfonyl Thiazoles -[using a modified Hantzsch thiazole synthesis]. -(BHINGOLIKAR, V. E.; MAHALLE, S. R.; BONDGE, S. P.; MANE*, R. A.; Indian J. Chem., Sect. B: Org.
A Facile Synthesis of New 6-Acetamido-3-aroyl-2-styryl Chromones. -The title compounds (V) are prepared to study the effect of acetamido and styryl moieties on the biological activity. -(BONDGE, S. P.; MAHALLE, S. R.; BURUNGALE, A. S.; PATIL, L. R.; MANE*, R. A.; Indian J.
Rapid, quantitative and regioselective O-acylation/O-benzoylation of hydroxamic acids has been carried using polymer supported hydroxamate anions and acetyl/benzoyl chloride under mild conditions. The isolation of unambiguous and pure products by simple work-up is also an important feature of this method.
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