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双核锌协同催化不对称膦-Michael/Michael 级联反应:含磷酰基的 1,2,3-三取代茚满的合成。

Dinuclear zinc synergistic catalytic asymmetric phospha-Michael/Michael cascade reaction: synthesis of 1,2,3-trisubstituted indanes bearing phosphoryl groups.

机构信息

College of Chemistry and Molecular Engineering, School of Pharmaceutical Sciences, Zhengzhou University, No. 100, Science Road, Zhengzhou City, Henan province 450000, P. R. China.

出版信息

Org Biomol Chem. 2019 Apr 24;17(17):4301-4310. doi: 10.1039/c9ob00544g.

Abstract

A new dinuclear zinc synergistic catalytic asymmetric phospha-Michael/Michael cascade reaction of o-dienones and dialkyl phosphates is reported. This method has been proven to be general and efficient for the formation of a range of chiral 1,2,3-trisubstituted indane compounds containing phosphorus groups in good yields (up to 92%) with excellent stereoselectivities (up to >99% ee and up to >99 : 1 dr). The relative configuration of the product was identified as having a trans,trans substitution pattern via two-dimensional (2D) nuclear Overhauser effect spectroscopy 1H-1H NMR experiments. A possible mechanism was proposed.

摘要

报道了一种新型双核锌协同催化不对称膦-Michael/Michael 级联反应,用于邻二烯酮和二烷基磷酸酯的反应。该方法已被证明对一系列手性 1,2,3-三取代茚烷化合物的形成具有普遍性和高效性,收率高(高达 92%),立体选择性好(高达 >99%ee 和高达 >99 : 1 dr)。通过二维(2D)核 Overhauser 效应光谱 1H-1H NMR 实验确定产物的相对构型为具有 trans,trans 取代模式。提出了一种可能的机制。

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