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Mendeleev Communications, 1995, Volume 5, Issue 1, Pages 18–20
DOI: https://doi.org/10.1070/MC1995v005n01ABEH000441
(Mi mendc5015)
 

This article is cited in 10 scientific papers (total in 10 papers)

An Approach to 8-, 16- and 24-Membered Sulfur-containing Heterocycles via Homolytic Cycloaddition of Alkynes with Butane-1,4-dithiol

E. I. Troyanskiia, R. F. Ismagilovb, E. N. Korneevab, M. S. Pogosyana, G. I. Nikishina

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
Abstract: Homolytic cycloaddition of butane-1,4-dithiol with alkynes offers a facile one-pot route to 8-membered 1,4-dithiocanes and 16-and 24-membered crown thioethers, 1,4,9,12-tetrathiacyclohexadecanes and 1,4,9,12,17,20-hexathiacyclotetracosanes.
Document Type: Article
Language: English


Citation: E. I. Troyanskii, R. F. Ismagilov, E. N. Korneeva, M. S. Pogosyan, G. I. Nikishin, “An Approach to 8-, 16- and 24-Membered Sulfur-containing Heterocycles via Homolytic Cycloaddition of Alkynes with Butane-1,4-dithiol”, Mendeleev Commun., 5:1 (1995), 18–20
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  • https://www.mathnet.ru/eng/mendc/v5/i1/p18
  • This publication is cited in the following 10 articles:
    1. George R. Newkome, Charles N. Moorefield, Comprehensive Heterocyclic Chemistry IV, 2022, 258  crossref
    2. L. Germán López-Valdez, Holber Zuleta-Prada, Benito Reyes-Trejo, Erick Cuevas-Yañez, “Synthesis of 10-membered and larger rings via free radical methods”, Tetrahedron, 74:14 (2018), 1581  crossref
    3. Cristina Lluch, Braulio Esteve‐Zarzoso, Albert Bordons, Gerard Lligadas, Juan C. Ronda, Marina Galià, Virginia Cádiz, “Antimicrobial Polyurethane Thermosets Based on Undecylenic Acid: Synthesis and Evaluation”, Macromolecular Bioscience, 14:8 (2014), 1170  crossref
    4. Samir Kundu, Babli Roy, Basudeb Basu, “Silica: An efficient catalyst for one-pot regioselective synthesis of dithioethers”, Beilstein J. Org. Chem., 10 (2014), 26  crossref
    5. Zhuang Jin, Bo Xu, Gerald B. Hammond, “Green Synthesis of Vicinal Dithioethers and Alkenyl Thioethers from the Reaction of Alkynes and Thiols in Water”, Eur J Org Chem, 2010:1 (2010), 168  crossref
    6. V. V. Litvinova, A. V. Anisimov, “Thiacrown compounds: Synthesis and properties. (Review)”, Chem Heterocycl Compd, 35:12 (1999), 1385  crossref
    7. E. I. Troyansky, D. V. Demchuk, G. I. Nikishin, “Homolytic addition of dithiols to alkynes: A new approach to the construction of dithiacyclanes and crown thioethers”, Russ Chem Bull, 46:7 (1997), 1199  crossref
    8. E. I. Troyanskii, M. S. Pogosyan, N. M. Samoshina, G. I. Nikishin, V. V. Samoshin, L. K. Shpigun, N. E. Kopytova, P. M. Kamilova, “Crown thioethers and 1,4-dithiacyclanes immobilized on silica carrier: preparation and studies of complexation affinity towards metal ions”, Mendeleev Commun., 6:1 (1996), 9–11  mathnet  crossref
    9. Emmanuil I. Troyansky, Rustem F. Ismagilov, Yury A. Strelenko, Vyacheslav V. Samoshin, Dmitry V. Demchuk, Gennady I. Nikishin, Sergey V. Lindeman, Viktor V. Khrustalyov, Yury T. Struchkov, “Remote asymmetric induction in free radical cycloaddition leading to trans-cyclohexano-fused 12-membered crown thioethers”, Tetrahedron Letters, 36:13 (1995), 2293  crossref
    10. Emmanuil I. Troyansky, Rustem F. Ismagilov, Vyacheslav V. Samoshin, Yury A. Strelenko, Dmitry V. Demchuk, Gennady I. Nikishin, Sergey V. Lindeman, Viktor N. Khrustalyov, Yury T. Struchkov, “Stereoselective free radical cycloaddition-macrocyclization in facile synthesis of trans-cyclohexano-fused 12-membered crown thioethers”, Tetrahedron, 51:42 (1995), 11431  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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