Abstract:
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.
Document Type:
Article
Language: English
Citation:
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
Linking options:
https://www.mathnet.ru/eng/mendc3938
https://www.mathnet.ru/eng/mendc/v13/i1/p21
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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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