Synthesis of novel tryptophan derivatives of potential biological activity

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Sociedad Chilena De Quimica

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Journal of the Chilean Chemical Society;vol.54 , no.2

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Abstract

Tryptophan methyl ester 2 reacts with ethyl cyanoacetate to form acetonitrilocarbonyltryptophan methylester 3. The latter reacts with cyanomethylene reagents, hydrazines, cyanomethylenes and sulfur to form the corresponding ?-pyrido-3-indolopropanoate derivatives 6a,b, pyrazolyltryptophan methyl ester derivatives 8a,b and thiophenotryptophan methyl ester derivatives 10a,b, respectively. Also compound 3 reacts with benzaldehyde to give the condensated product 12. The reactivity of the latter product towards chemical reagents was studied to form pyridine, pyrazole and isoxazole derivatives.

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SJR 2024 0.307 Q3 H-Index 44

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MOHAREB, R. M., LOUCA, N. A., ELMEGEED, G. A., & HANA, H. Y. (2009). SYNTHESIS OF NOVEL TRYPTOPHAN DERIVATIVES OF POTENTIAL BIOLOGICAL ACTIVITY. Journal of the Chilean Chemical Society, 54(2). https://doi.org/10.4067/s0717-97072009000200018 ‌

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