E. I. Troyanskii, D. V. Demchuk, M. I. Lazareva, V. V. Samoshin, Yu. A. Strelenko, G. I. Nikishin, “Macrocyclization with Participation of ThiyI Radicals: Construction of 18- and 9-Membered Crown Thioethers”, Mendeleev Commun., 2:2 (1992), 48

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Mendeleev Communications, 1992, Volume 2, Issue 2, Pages 48–49
DOI: https://doi.org/10.1070/MC1992v002n02ABEH000124 (Mi mendc5395)

This article is cited in 13 scientific papers (total in 13 papers)

Macrocyclization with Participation of ThiyI Radicals: Construction of 18- and 9-Membered Crown Thioethers

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

^a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
^b Department of Chemistry, University of the Pacific, Stockton, California, USA

Full-text PDF (293 kB) Citations (13)

DOI: https://doi.org/10.1070/MC1992v002n02ABEH000124

Abstract: A one-pot synthesis of crown thioethers, 1,10-dioxa-4,7,13,16-tetrathiacyclooctadecanes and 1-oxa-4,7-dithiacyclononanes, which are the 2:2 and 1:1 cycloadducts of the homolytic macrocyclization of alkynes with 3-oxapentane-1,5-dithiol, has been developed.

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Document Type: Article

Language: English

Citation: E. I. Troyanskii, D. V. Demchuk, M. I. Lazareva, V. V. Samoshin, Yu. A. Strelenko, G. I. Nikishin, “Macrocyclization with Participation of ThiyI Radicals: Construction of 18- and 9-Membered Crown Thioethers”, Mendeleev Commun., 2:2 (1992), 48–49

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https://www.mathnet.ru/eng/mendc/v2/i2/p48

This publication is cited in the following 13 articles:

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