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 α-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.
CITATION STYLE
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), 175–179. https://doi.org/10.4067/S0717-97072009000200018
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