首页> 外文期刊>Journal of the American Chemical Society >Enantioselective Synthesis of syn- and anti-1,3-Aminoalcohols via β-Aminoketones and Subsequent Reduction/Dynamic Kinetic Asymmetric Transformation
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Enantioselective Synthesis of syn- and anti-1,3-Aminoalcohols via β-Aminoketones and Subsequent Reduction/Dynamic Kinetic Asymmetric Transformation

机译:通过β-氨基酮和随后的还原/动力学动力学不对称转化反应,对映选择性合成顺式和反式1,3-氨基醇

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摘要

β-Aminoketones obtained from imines in an organocatalytic Mannich reaction were transformed to enantio- and diastereomerically pure 1,3-aminoalcohols with two stereogenic centers via a combined reduction/dynamic kinetic asymmetric transformation. Both syn and anti diastereomers were obtained in high yield, dr, and ee.
机译:在有机催化曼尼希反应中从亚胺获得的β-氨基酮通过还原/动态动力学不对称转化相结合,转化为具有两个立体中心的对映体和非对映体纯的1,3-氨基醇。 syn和抗非对映异构体均以高收率(dr和ee)获得。

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