Electrophilic addition of butyl chloride to 2-allylphenol in the presence of sulfur trioxide
AM Magerramov, MP Bairamov, IG Mamedov…
Index: Magerramov; Bairamov; Mamedov; Dzhavadov Russian Journal of Organic Chemistry, 2002 , vol. 38, # 8 p. 1210 - 1211
Full Text: HTML
Citation Number: 1
Abstract
Evidence was reported [133] on insertion of sulfur trioxide into ordinary element3element bonds providing new reagents of high electrophilicity capable of addition to unsaturated systems [4]. The aim of this study was extension of sulfonate activation strategy to increasing electrophilic reactivity of chlorination and alkylation agents by an example of reaction between butyl chloride and 2-allylphenol in the presence of sulfur trioxide.
Related Articles:
[Olah,G.A.; Nishimura,J. Journal of the American Chemical Society, 1974 , vol. 96, p. 2214 - 2220 View citing articles Show Details Binkley; Degering Journal of the American Chemical Society, 1938 , vol. 60, p. 2810 View citing articles Show Details Barkenbus; Owen Journal of the American Chemical Society, 1934 , vol. 56, p. 1206 Show Details Levaillant Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1933 , vol. 197, p. 335 Annales de Chimie (Cachan, France), 1936 , vol. <11>6, p. 495]