首页> 外文期刊>Organic letters >C-2-Symmetric Chiral Bisoxazolines as Hydrogen-Bond-Acceptor Catalysts in Enantioselective Aldol Reaction of beta-Carbonyl Acids with Trifluoroacetaldehyde Hemiacetals
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C-2-Symmetric Chiral Bisoxazolines as Hydrogen-Bond-Acceptor Catalysts in Enantioselective Aldol Reaction of beta-Carbonyl Acids with Trifluoroacetaldehyde Hemiacetals

机译:C-2-对称的手性联二恶唑啉作为β-羰基酸与三氟乙醛半缩醛的对映选择性醛醇缩合反应中的氢键受体催化剂

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摘要

A simple C-2-symmetric chiral bisoxazoline is demonstrated to use hydrogen bonding to catalyze an important family of aldol reactions of trifluoroacetaldehyde hemiacetals with various beta-carbonyl acids. This reaction is highly enantioselective, delivering chiral nonracemic trifluoromethylated alcohols with excellent optical purity and good isolated yields. This concept of relaying chiral information via a chiral hydrogen-bond acceptor should be applicable to a vast number of organo catalytic processes.
机译:一个简单的C-2-对称手性双恶唑啉被证明使用氢键催化三氟乙醛半缩醛与各种β-羰基酸的重要的醛醇缩合反应家族。该反应是高度对映体选择性的,以优异的光学纯度和良好的分离产率提供手性非外消旋三氟甲基化醇。通过手性氢键受体传递手性信息的概念应适用于大量有机催化过程。

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