An expeditious green synthesis of Schiff bases and azetidinones derivatised with 1,2,4-triazoles

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Abstract

An efficient green approach to the synthesis of Schiff bases (11-21) of 1-amino-2-aryl-3-oxo-1,2,4- triazoles (1-3) have been reported under Mg(ClO 4)2 as catalyst followed by the reaction with chloroacetyl chloride in solvent-free conditions to yield the azetidinones (22-32) with excellent yields. The synthesized compounds were evaluated for the extent of penetration into biological membranes (clogP), drug-likeliness and finally drug score was calculated and also screened for antitubercular and antimicrobial activities. © Indian Academy of Sciences.

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Taj, T., Kamble, R. R., Gireesh, T., & Badami, B. V. (2011). An expeditious green synthesis of Schiff bases and azetidinones derivatised with 1,2,4-triazoles. Journal of Chemical Sciences, 123(5), 657–666. https://doi.org/10.1007/s12039-011-0138-8

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