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.
Тип публикации:
Статья
Язык публикации: английский
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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Zhen Wang, Xuefei Huang, Encyclopedia of Reagents for Organic Synthesis, 2008
William A. Smit, Alexei V. Gromov, Elisey A. Yagodkin, “Adducts of ArSCl with Vinyl Ethers or Esters as Synthones in Geminal Alkylation.”, ChemInform, 34:31 (2003)
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