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钯催化的二芳基膦对α,β-不饱和醛的 1,4-加成反应。

Palladium-catalyzed 1,4-addition of diarylphosphines to α,β-unsaturated aldehydes.

机构信息

State Key Laboratory of Organometallic Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.

出版信息

Org Lett. 2011 Nov 4;13(21):5824-6. doi: 10.1021/ol2024339. Epub 2011 Oct 6.

DOI:10.1021/ol2024339
PMID:21977906
Abstract

A highly stereoselective asymmetric 1,4-addition of diarylphosphines to α,β-unsaturated aldehydes catalyzed by a bis(phosphine) pincer-Pd complex has been developed for the synthesis of chiral phosphines with excellent stereoselectivity (up to 98% ee) under mild conditions. The application of the current method to the synthesis of enantiopure bisphosphine and its pincer-Pd complex has also been demonstrated.

摘要

一种双(膦)钳钯配合物催化的二芳基膦对α,β-不饱和醛的高对映选择性 1,4-加成反应已被开发出来,用于在温和条件下以优异的对映选择性(高达 98%ee)合成手性膦。该方法在手性双膦及其钳钯配合物的合成中的应用也得到了证明。

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