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Эта публикация цитируется в 5 научных статьях (всего в 5 статьях)
Adducts of ArSCl with vinyl ethers or esters as synthones in geminal alkylation
W. A. Smita, A. V. Gromovb, E. A. Yagodkina a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b Higher Chemical College of the Russian Academy of Sciences, D.I. Mendeleev University of Chemical Technology of Russia, Moscow, Russian Federation
Аннотация:
The in situ-prepared adducts of arylsulfenyl chloride and vinyl ethers (esters) were employed as synthetic equivalents of 1,1-bis-electrophiles in the Lewis acid-promoted reaction sequence with two different carbon nucleophiles resulting in the formation of geminal bisalkylation products.
Образец цитирования:
W. A. Smit, A. V. Gromov, E. A. Yagodkin, “Adducts of ArSCl with vinyl ethers or esters as synthones in geminal alkylation”, Mendeleev Commun., 13:1 (2003), 21–23
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc3938 https://www.mathnet.ru/rus/mendc/v13/i1/p21
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