Design and Synthesis of substituted oxazolones and their antibacterial activity

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ECSOC-13 | Bioorganic Chemistry and Natural Products

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13th Int. Electron. Conf. Synth. Org. Chem. 2009, c025:1-7

Communication

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Design and Synthesis of substituted oxazolones and their antibacterial activity

Mohd. Shahnawaaz*

, Arshi Naqvi, A.V. Rao and D. S. Seth

Chemistry Department, St. John’s College, Agra-282002, India; * Author to whom correspondence should be addressed.

(This article belongs to the section C. Bioorganic Chemistry and Natural Products)

Cite this paper as: Shahnawaaz, M.; Naqvi, A.; Rao, A.; Seth, D. Design and Synthesis of substituted oxazolones and their antibacterial activity. In Proceedings of the 13th Int. Electron. Conf. Synth. Org. Chem., 1-30 November 2009; Sciforum Electronic Conferences Series, 2009, c025:1-7.

Abstract: A great deal of work has been done on the synthesis of oxazolones. We have obtained 5(4H)-oxazolones by condensing anthracene-10-carbaldehyde & furan-2- carbaldehyde with a number of substituted benzoyl glycines, and tried to design new and effective anti-bacterial agents.

Keywords: Substituted oxazolones, substituted benzoyl glycines, substituted aromatic aldehydes, anti-bacterial activity

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