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Lipase-Catalyzed Stereoselective Cross-Aldol Reaction Promoted by Water

Journal 2013 · IF 5.181 · 5(7): 1935-1940 · 发表于 2013 年 3 月 7 日
作者: Zong-Bo Xie,Na Wang,Long-Hua Zhou,Fang Wan,Ting He,Zhang-Gao Le,Xiao-Qi Yu
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摘要

Graphical Lip synthing: A lipase-catalyzed, green, and efficient approach for the cross-aldol reaction promoted by water with high yield and good stereoselectivity is described. PPL, lipase from porcine pancreas, is first reported to catalyze direct asymmetric aldol reactions between aromatic aldehydes and cyclic ketones. More importantly, the catalytic activity of PPL was greatly promoted by a small quantity of water at 37 °C. A wide range of aromatic aldehydes reacted with cyclic ketones to provide the corresponding aldol products with high yields (up to 99 %) and moderate to good stereoselectivity (up to 90 % ee and 99:1 dr ).

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