E. I. Troyanskii, D. V. Demchuk, R. F. Ismagilov, M. I. Lazareva, Yu. A. Strelenko, G. I. Nikishin, “Homolytic Macrocyclization of Alkynes with Propane-1,3-dithiol as a Route to 14- and 21-Membered Crown Thioethers”, Mendeleev Commun., 3:3 (1993), 112

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Mendeleev Communications, 1993, Volume 3, Issue 3, Pages 112–114
DOI: https://doi.org/10.1070/MC1993v003n03ABEH000248 (Mi mendc5291)

This article is cited in 11 scientific papers (total in 11 papers)

Homolytic Macrocyclization of Alkynes with Propane-1,3-dithiol as a Route to 14- and 21-Membered Crown Thioethers

E. I. Troyanskii^a, D. V. Demchuk^a, R. F. Ismagilov^b, M. I. Lazareva^a, Yu. A. Strelenko^a, G. I. Nikishin^a

^a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
^b Higher Chemical College of the Russian Academy of Sciences, D.I. Mendeleev University of Chemical Technology of Russia, Moscow, Russian Federation

Full-text PDF (337 kB) Citations (11)

DOI: https://doi.org/10.1070/MC1993v003n03ABEH000248

Abstract: Crown thioethers, 1,4,8,11-tetrathiacyclotetradecanes and 1,4,8,11,15,18-hexathiaheneicosanes, have been synthesized as 2:2 and 3:3 cycloadducts in a ‘one-pot’ homolytic macrocyclization of alkynes with propane-1,3-dithiol.

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Document Type: Article

Language: English

Citation: E. I. Troyanskii, D. V. Demchuk, R. F. Ismagilov, M. I. Lazareva, Yu. A. Strelenko, G. I. Nikishin, “Homolytic Macrocyclization of Alkynes with Propane-1,3-dithiol as a Route to 14- and 21-Membered Crown Thioethers”, Mendeleev Commun., 3:3 (1993), 112–114

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https://www.mathnet.ru/eng/mendc/v3/i3/p112

This publication is cited in the following 11 articles:

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