Abstract
Azomethine ylides were generated from Schiffs bases of S-allylcysteine methyl ester and their intramolecular 1,3-dipolar cycloadditions were studied. These reactions led to the synthesis of thieno[3,4-b]pyrrole derivatives in good yield.
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APA
Cabral, A. M. T. D. P. V., D’A Rocha Gonsalves, A. M., & Pinho E Melo, T. M. V. D. (1998). Intramolecular cycloaddition of imines of cysteine derivatives. In Molecules (Vol. 3, pp. 60–63). Molecular Diversity Preservation International. https://doi.org/10.3390/30300060
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