Low-Valent Niobium-Mediated Double Activation of CF/CH Bonds: Fluorene Synthesis from o-Arylated α, α, α-Trifluorotoluene Derivatives
K Fuchibe, T Akiyama
Index: Fuchibe, Kohei; Akiyama, Takahiko Journal of the American Chemical Society, 2006 , vol. 128, # 5 p. 1434 - 1435
Full Text: HTML
Citation Number: 123
Abstract
The C−F bond is the strongest single bond connected to carbon. 1 Although several aromatic and aliphatic C−F bond activations have been reported in recent years, 2,3 the development of a novel method for C−F bond activation remains elusive. In particular, the CF 3 group attached to an aromatic ring is surprisingly stable, and the activation of these benzylic C−F bonds is quite limited. 4 The transformation of the CF 3 groups is thus a challenging task from the ...
Related Articles:
[Robertson; Krushinski; Beedle; Leander; Wong; Rathbun Journal of Medicinal Chemistry, 1986 , vol. 29, # 9 p. 1577 - 1586]
Direct catalytic cross-coupling of organolithium compounds
[Giannerini, Massimo; Fananas-Mastral, Martin; Feringa, Ben L. Nature Chemistry, 2013 , vol. 5, # 8 p. 667 - 672]
An NMR investigation of the Mills-Nixon effect
[Collins, Michael J.; Gready, Jill E.; Sternhell, Sever; Tansey, Charles W. Australian Journal of Chemistry, 1990 , vol. 43, p. 1547 - 1557]
Carbene-carbene rearrangements
[Jones,W.M. et al. Journal of the American Chemical Society, 1973 , vol. 95, p. 826 - 835]
An NMR investigation of the Mills-Nixon effect
[Collins, Michael J.; Gready, Jill E.; Sternhell, Sever; Tansey, Charles W. Australian Journal of Chemistry, 1990 , vol. 43, p. 1547 - 1557]