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Mendeleev Communications, 1994, Volume 4, Issue 6, Pages 225–226
DOI: https://doi.org/10.1070/MC1994v004n06ABEH000426
(Mi mendc5230)
 

This article is cited in 1 scientific paper (total in 1 paper)

Ring Opening of Persubstituted 4H-Thiopyran 1-Oxide During Chlorination

P. Sebeka, J. Kroulika, M. Husakb, P. Sedmerac, V. Havlicekc, B. Kratochvilb, J. Kuthana

a Department of Organic Chemistry, Institute of Chemical Technology, Prague, Czech Republic
b Department of Solid State Chemistry, Institute of Chemical Technology, Prague, Czech Republic
c Institute of Microbiology, Academy of Science of the Czech Republic, Prague
Full-text PDF (253 kB) Citations (1)
Abstract: Chlorination of 3,5-dichloro-2,4,4,6-tetraphenyl-4H-thiopyran 1-oxide 3(CI2 in CS2,20°C) followed byalcoholysis (EtOH, MeOH) gives ethyl or methyl (1E,4E)-1,4,5-trichloro-1,3,3,5-tetraphenylpenta-1,4-diene-1-sulfinates 5 and 6, respectively; the structure of 5 has been determined by X-ray analysis.
Document Type: Article
Language: English


Citation: P. Sebek, J. Kroulik, M. Husak, P. Sedmera, V. Havlicek, B. Kratochvil, J. Kuthan, “Ring Opening of Persubstituted 4H-Thiopyran 1-Oxide During Chlorination”, Mendeleev Commun., 4:6 (1994), 225–226
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  • https://www.mathnet.ru/eng/mendc5230
  • https://www.mathnet.ru/eng/mendc/v4/i6/p225
  • This publication is cited in the following 1 articles:
    1. P. SEBEK, J. KROULIK, M. HUSAK, P. SEDMERA, V. HAVLICEK, B. KRATOCHVIL, J. KUTHAN, “ChemInform Abstract: Ring Opening of Persubstituted 4H‐Thiopyran 1‐Oxide During Chlorination.”, ChemInform, 26:18 (1995)  crossref
    Citing articles in Google Scholar: Russian citations, English citations
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