Deprotonative C–H Silylation of Functionalized Arenes and Heteroarenes Using Trifluoromethyltrialkylsilane with Fluoride
M Sasaki, Y Kondo
Index: Taneda, Hiroshi; Inamoto, Kiyofumi; Kondo, Yoshinori Chemical Communications, 2014 , vol. 50, # 49 p. 6523 - 6525
Full Text: HTML
Citation Number: 4
Abstract
A highly selective C–H silylation reaction of functionalized arenes and heteroarenes was developed using Ruppert–Prakash reagent (TMSCF3) activated by alkali metal fluoride. TMSCF3 is considered to play dual roles as a precursor of a mild base and also as a silicon
Related Articles:
[Dicken, C. Michael; Lu, Fu-Lung; Nee, Michael W.; Bruice, Thomas C. Journal of the American Chemical Society, 1985 , vol. 107, # 20 p. 5776 - 5789]
[Wong, Wah-Hun; Ostovic, Drazen; Bruice, Thomas C. Journal of the American Chemical Society, 1987 , vol. 109, # 11 p. 3428 - 3436]
[Dicken, C. Michael; Lu, Fu-Lung; Nee, Michael W.; Bruice, Thomas C. Journal of the American Chemical Society, 1985 , vol. 107, # 20 p. 5776 - 5789]
[Dicken, C. Michael; Lu, Fu-Lung; Nee, Michael W.; Bruice, Thomas C. Journal of the American Chemical Society, 1985 , vol. 107, # 20 p. 5776 - 5789]
[Dicken, C. Michael; Lu, Fu-Lung; Nee, Michael W.; Bruice, Thomas C. Journal of the American Chemical Society, 1985 , vol. 107, # 20 p. 5776 - 5789]