1236142-26-9Relevant academic research and scientific papers
Carbon acid induced mukaiyama aldol type reaction of sterically hindered ketones
Yanai, Hikaru,Yoshino, Yasuhiro,Takahashi, Arata,Taguchi, Takeo
, p. 5375 - 5378 (2010)
(Figure presented) 1,1,3,3-Tetrakis(trifluoromethanesulfonyl)propane (Tf2CHCH2CHTf2) is one of the most effective Bronsted acid precatalysts for the Mukaiyama aldol type reactions of sterically hindered ketones. By using Tf2CHCH2CHTf 2 in a range from 0.5 to 2.0 mol %, the vinylogous Mukaiyama aldol reaction of α-substituted cyclohexanones with 2-silyloxyfurans smoothly proceeded to give the aldol products in excellent yield without the loss of diastereoselectivity. Under similar conditions, acyclic ketene silyl acetals also performed as nice nucleophiles toward sterically hindered ketones. These findings suggest that Tf2CHCH2CHTf2 induced Mukaiyama aldol type reactions can overcome the steric hindrance between reaction sites.
