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手性二烯作为配体,通过钯催化的 Suzuki-Miyaura 偶联反应合成轴手性化合物。

Chiral diene as the ligand for the synthesis of axially chiral compounds via palladium-catalyzed Suzuki-Miyaura coupling reaction.

机构信息

Key Laboratory of Synthetic Chemistry of Natural Substances, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 345 Lingling Road, Shanghai 200032, China.

出版信息

Org Lett. 2010 Dec 3;12(23):5546-9. doi: 10.1021/ol102521q. Epub 2010 Nov 11.

Abstract

The first palladium-diene-catalyzed asymmetric Suzuki-Miyaura coupling reaction has been achieved. A number of functionalized biaryls were obtained in high yields and in moderate to high enantioselectivities. The existence of an ortho-formyl group greatly improves the catalyst efficiency and permits further synthetic elaborations.

摘要

首例钯-二烯催化的不对称铃木-宫浦偶联反应已经实现。许多功能化联芳基以高产率和中等至高产率获得了较高的对映选择性。邻甲酰基的存在极大地提高了催化剂的效率,并允许进一步的合成修饰。

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