Abstract
Noncatalyzed, regio-And stereoselective hypochlorite oxidation of 3-Aminothieno[2,3-b]pyridine-2-carboxamides is presented. Unexpectedly, the oxidation proceeded by different mechanistic pathways, and different products were formed, depending on the nature of solvents used. A possible mechanism, the structure of products, kinetics and dynamics of intramolecular processes, and biological activity of products are discussed.
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CITATION STYLE
Stroganova, T. A., Vasilin, V. K., Dotsenko, V. V., Aksenov, N. A., Morozov, P. G., Vassiliev, P. M., … Krapivin, G. D. (2021). Unusual Oxidative Dimerization in the 3-Aminothieno[2,3-b]pyridine-2-carboxamide Series. ACS Omega, 6(22), 14030–14048. https://doi.org/10.1021/acsomega.1c00341
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