Please use this identifier to cite or link to this item: http://nopr.niscair.res.in/handle/123456789/6486
Title: Synthesis of some novel 4-substituted coumarins having potential biological activity (Part III)
Authors: Mashelka, U C
Audi, A A
Keywords: Schiff bases
thioglycolic acid 4-thiazolidinone
oxadiazoles and thiadiazoles
polyphosphoric acid
Issue Date: Jun-2006
Publisher: CSIR
Series/Report no.: <b>Int.Cl.<sup>8</sup> C07D</b>
Abstract: Various methyl substituted coumarin carboxaldehydes have been condensed with aromatic amines to give Schiff bases. These Schiff bases have then been reacted with thioglycolic acid to give five membered cyclized products, 4-thiazolidinone substituted at 4-position of coumarins. 4-alkyl coumarin acetates have been reacted with semicarbazide or thiosemicarbazide in polyphosphoric acid to undergo condensation followed by <i>in situ</i> cyclization to form oxadiazoles and thiadiazoles. All the 4 – substituted coumarin heterocycles have been found to possess antibacterial activity.
Description: 1463-1469
URI: http://hdl.handle.net/123456789/6486
ISSN: 0975-0983(Online); 0376-4699(Print)
Appears in Collections:IJC-B Vol.45B(06) [June 2006]

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