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JOURNALS // Mendeleev Communications // Archive

Mendeleev Commun., 1992 Volume 2, Issue 2, Pages 48–49 (Mi mendc5395)

This article is cited in 13 papers

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

E. I. Troyanskiia, D. V. Demchuka, M. I. Lazarevaa, V. V. Samoshinb, Yu. A. Strelenkoa, G. I. Nikishina

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

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.

Language: English

DOI: 10.1070/MC1992v002n02ABEH000124



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