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首页> 外文期刊>Tetrahedron, Asymmetry: The International Journal for Repid Publication on all Aspects of Asymmetry in Orgainc, Inorganic, Organometallic, Physical and Bio-Organic Chemistry >Aqua-organocatalyzed direct asymmetric aldol reaction with acyclic amino acids and organic bases with control of diastereo- and enantioselectivity
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Aqua-organocatalyzed direct asymmetric aldol reaction with acyclic amino acids and organic bases with control of diastereo- and enantioselectivity

机译:在非对映和对映选择性的控制下,与无环氨基酸和有机碱进行水族有机催化的直接不对称羟醛缩合反应

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摘要

An effective aqua-organocatalytic direct aldol reaction is described. Aromatic amino acids can be a bifunctional catalyst system, which demonstrate excellent reactivity, diastereoselectivity, and enantioselectivity (up to 96% ee) in water without the addition of organic solvents. Furthermore, the present study demonstrates that both diastereo and enantioselectivity can be easily modulated by the appropriate combination of an organocatalyst together with an organic base as a co-catalyst. (c) 2007 Elsevier Ltd. All rights reserved.
机译:描述了有效的水-有机催化直接羟醛反应。芳族氨基酸可以是双功能催化剂体系,在水中无需添加有机溶剂即可表现出出色的反应性,非对映选择性和对映选择性(最高96%ee)。此外,本研究表明,通过有机催化剂与有机碱作为助催化剂的适当组合,可以轻松调节非对映选择性和对映选择性。 (c)2007 Elsevier Ltd.保留所有权利。

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