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This article is cited in 7 scientific papers (total in 7 papers)
Thienopentathiepins and pentathiepinofuran
S. A. Amelicheva, L. S. Konstantinovaa, O. A. Rakitina, Ch. W. Reesb a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b Department of Chemistry, Imperial College London, London, UK
Abstract:
Thienopentathiepins and pentathiepinofuran were synthesised by the reaction of thiophenes and 2,5-dimethylfuran with S2Cl2 and N-ethyldiisopropylamine in chloroform at low temperature; thienopentathiepin 2 reacts with methyl propiolate and triphenylphosphine to give a pair of regioisomers.
Citation:
S. A. Amelichev, L. S. Konstantinova, O. A. Rakitin, Ch. W. Rees, “Thienopentathiepins and pentathiepinofuran”, Mendeleev Commun., 16:6 (2006), 289–290
Linking options:
https://www.mathnet.ru/eng/mendc3628 https://www.mathnet.ru/eng/mendc/v16/i6/p289
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