化学
迈克尔反应
组合化学
立体化学
有机化学
催化作用
作者
Huidan Fan,Cong‐Hai Zhang,Sheng‐Jiao Yan,Lin Jun
摘要
Chiral auxiliaries controlled asymmetric reaction is one of the main methods in asymmetric synthesis.Under the control of the Evans auxiliary and catalyzed by FeCl 3 , different Grignard reagents were added asymmetrically to the substrates 1 by the way of 1,4-Michael addition reaction, and a series of Michael addition products 2a~2h which containing two chiral centers have been synthesized with higher stereoselectivity.Among them, compounds 2d and 2e achieved high diastereospecifically up to 98% de.The results showed that the steric hindrance of the Grignard reagents is the main factor which influences the stereoselectivity of Micheal addition.
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