Abstract
The review summarizes published data on the reactions of cyclic and acyclic thioamides with derivatives of acetylenecarboxylic acids, which lead to the formation of both acyclic and heterocyclic systems, including thiazolidines and thiazines. Methods for determination of the structure of the condensation products and factors responsible for the reaction direction are discussed.
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Original Russian Text © N.A. Danilkina, L.E. Mikhailov, B.A. Ivin, 2006, published in Zhurnal Organicheskoi Khimii, 2006, Vol. 42, No. 6, pp. 807–839.
Natal’ya Danilkina graduated from the Pharmaceutical Faculty, St. Petersburg Chemical and Pharmaceutical Academy, in 2003 and entered post-graduate courses at the Organic Chemistry Department, St. Petersburg Chemical and Pharmaceutical Academy. In 2004, she was a J. Soros’ post-graduate student. Fields of scientific interest: chemistry of heterocyclic compounds and application of NMR for studying the structure of heterocycles.
Leonid Mikhailov graduated from the Faculty of Chemistry, Leningrad State University, in 1989. In 1995–1998, he was a post-graduate student at the Organic Chemistry Department, St. Petersburg Chemical and Pharmaceutical Academy, where he sustained his Candidate’s Theses in 1998. L. Mikhailov works now at the Department of Dyes and Phototropic Compounds, St. Petersburg State Institute of Technology. Field of scientific interest: chemistry of biologically active heterocyclic compounds.
Boris Ivin is Doctor of Chemical Sciences, Professor, Honored Scientific Worker of the Russian Federation, Head of the Organic Chemistry Department, St. Petersburg Chemical and Pharmaceutical Academy. Fields of scientific interest: chemistry of heterocyclic compounds, medicinal chemistry, and relations between the structure and biological activity of organic compounds.
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Danilkina, N.A., Mikhailov, L.E. & Ivin, B.A. Condensations of thioamides with acetylenecarboxylic acid derivatives. Russ J Org Chem 42, 783–814 (2006). https://doi.org/10.1134/S1070428006060017
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DOI: https://doi.org/10.1134/S1070428006060017