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ЖУРНАЛЫ // Mendeleev Communications // Архив

Mendeleev Commun., 1994, том 4, выпуск 6, страницы 225–226 (Mi mendc5230)

Эта публикация цитируется в 1 статье

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

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.

Язык публикации: английский

DOI: 10.1070/MC1994v004n06ABEH000426



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