Naphtho[2,1-b]furan-2-carbohydrazide (1) undergoes facile condensation with aromatic aldehydes to affo rd the corresponding N-arylidenenaphtho[2,1-b]furan-2-carb ohydrazide(3a-h) in good yields. Cyclocondensation of compounds (3a-h) with thioglycolic acid yields N-(4 -oxo-2-arylthiazolidin-3-yl) naphtho[2,1-b]furan-2- carboxamide (4a-h). The structures of these compoun ds were established on the basis of analytical and spectral data. All the newly synthesized compounds were eval uated for their antibacterial and antifungal activi ties
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