aDepartment of Organic Chemistry, Institute of Chemical Technology, Prague, Czech Republic bDepartment of Solid State Chemistry, Institute of Chemical Technology, Prague, Czech Republic cInstitute of Microbiology, Academy of Science of the Czech Republic, Prague
Аннотация:
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.
Тип публикации:
Статья
Язык публикации: английский
Образец цитирования:
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
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc5230
https://www.mathnet.ru/rus/mendc/v4/i6/p225
Эта публикация цитируется в следующих 1 статьяx:
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)
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