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镍催化烯烃的还原芳酰化反应合成含羰基的氧化吲哚

Ni-Catalyzed Reductive Arylacylation of Alkenes toward Carbonyl-Containing Oxindoles.

作者信息

Xu Sheng, Wang Kuai, Kong Wangqing

机构信息

The Center for Precision Synthesis (CPS), Institute for Advanced Studies (IAS) , Wuhan University , Wuhan 430072 , People's Republic of China.

出版信息

Org Lett. 2019 Sep 20;21(18):7498-7503. doi: 10.1021/acs.orglett.9b02788. Epub 2019 Sep 3.

DOI:10.1021/acs.orglett.9b02788
PMID:31479280
Abstract

An easy-to-handle Ni-catalyzed three-component reductive arylacylation of alkenes using isobutyl chloroformate as a CO source was described. This reaction operates under mild reaction conditions without the need to use toxic CO gas or metal carbonyl reagents. In addition, this method allows for rapid synthesis of 3,3-disubstituted oxindoles with an all-carbon quaternary stereocenter containing a ketone group in good yields with broad substrate scope.

摘要

描述了一种易于操作的镍催化的烯烃三组分还原芳基酰化反应,该反应使用氯甲酸异丁酯作为CO源。该反应在温和的反应条件下进行,无需使用有毒的CO气体或金属羰基试剂。此外,该方法能够快速合成具有全碳季碳立体中心且含有酮基的3,3-二取代氧化吲哚,产率良好,底物范围广泛。

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