首页> 外文期刊>Journal of the American Chemical Society >Multiple Absolute Stereocontrol in Cascade Lactone Formation via Dynamic Kinetic Resolution Driven by the Asymmetric Transfer Hydrogenation of Keto Acids with Oxo-Tethered Ruthenium Catalysts
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Multiple Absolute Stereocontrol in Cascade Lactone Formation via Dynamic Kinetic Resolution Driven by the Asymmetric Transfer Hydrogenation of Keto Acids with Oxo-Tethered Ruthenium Catalysts

机译:氧束缚钌催化剂催化酮酸的不对称转移加氢,通过动态动力学拆分驱动级联内酯形成中的多个绝对立体控制。

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摘要

A straightforward asymmetric construction of chiral fused gamma- and delta-lactones containing multiple contiguous stereocenters was successfully developed by either (1) the dynamic kinetic resolution-asymmetric transfer hydrogenation (DKR-ATH) reaction using oxo-tethered Ru(II) complexes followed by syn-selective lactonization or (2) the tandem DKR-ATH/lactonization in combination with asymmetric hydrogenation catalyzed by Ru-chiral diphosphine complexes. The expedient protocol is applicable to the enantioselective synthesis of natural wine lactone and a biologically active benzo-fused lactone with an unprecedented level of diastereo- and enantioselectivity.
机译:通过以下两种方法之一成功开发了一种简单的不对称结构,即含有多个连续立体中心的手性融合的γ-和δ-内酯,其方法是:(1)使用氧束缚的Ru(II)络合物进行动态动力学拆分-不对称转移氢化(DKR-ATH)反应,然后进行顺式选择性内酯化或(2)串联DKR-ATH /内酰胺化与Ru-手性二膦配合物催化的不对称氢化反应。方便的方案适用于天然酒内酯和具有非对映选择性和对映选择性的生物活性的苯并稠合内酯的对映选择性合成。

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