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铜催化的芳基硼酸对吲哚啉酮的不对称加成:涉及烷氧基铜中间体的催化循环。

Copper-catalyzed asymmetric addition of arylboronates to isatins: a catalytic cycle involving alkoxocopper intermediates.

机构信息

Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan.

出版信息

Chem Commun (Camb). 2010 Sep 28;46(36):6822-4. doi: 10.1039/c0cc01635g. Epub 2010 Aug 20.

Abstract

A copper-catalyzed addition of arylboronates to isatins has been developed to give 3-aryl-3-hydroxy-2-oxindoles under mild conditions. The catalytic cycle of this process has been examined through a series of stoichiometric reactions and an effective asymmetric variant has also been described by the use of a chiral N-heterocyclic carbene ligand.

摘要

发展了一种铜催化的芳基硼酸与色酮的加成反应,在温和条件下得到 3-芳基-3-羟基-2-氧吲哚。通过一系列的计量反应研究了这个催化循环,并且通过使用手性 N-杂环卡宾配体也描述了一种有效的不对称变体。

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