|
Эта публикация цитируется в 1 научной статье (всего 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.
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
|
|