1274835-65-2Relevant academic research and scientific papers
Lewis acid catalyzed benzylic C-H bond functionalization of azaarenes: Addition to enones
Komai, Hirotomo,Yoshino, Tatsuhiko,Matsunaga, Shigeki,Kanai, Motomu
, p. 1706 - 1709 (2011)
A Lewis acid catalyzed benzylic C-H bond functionalization of alkyl-substituted azaarenes is described. Sc(OTf)3 and Y(OTf) 3 promoted the direct addition of alkyl-substituted azaarenes and benzoxazole to enones and an α,β-unsaturate
Lewis acid catalyzed benzylic C-H bond functionalization of azaarenes; Addition to imines and enones
Komai, Hirotomo,Yoshino, Tatsuhiko,Matsunaga, Shigeki,Kanai, Motomu
experimental part, p. 2185 - 2194 (2012/10/08)
Lewis acid catalyzed benzylic C-H bond functionalization of alkyl-substituted azaarenes is described. The addition to N-tosyl imines proceeded under solvent-free conditions using various Lewis acids. Cu(OTf) 2 was the best Lewis acid, and 1,2-a
