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银催化的炔烃的立体选择性氨基磺酰化反应。

Silver-Catalyzed Stereoselective Aminosulfonylation of Alkynes.

机构信息

Jilin Province Key Laboratory of Organic Functional Molecular Design & Synthesis, Department of Chemistry, Northeast Normal University, Changchun, 130024, China.

Chemistry Research Laboratory, University of Oxford, 12 Mansfield Road, Oxford, OX1 3TA, UK.

出版信息

Angew Chem Int Ed Engl. 2017 Oct 23;56(44):13805-13808. doi: 10.1002/anie.201705122. Epub 2017 Jul 7.

Abstract

A silver-catalyzed intermolecular aminosulfonylation of terminal alkynes with sodium sulfinates and TMSN is reported. This three-component reaction proceeds through sequential hydroazidation of the terminal alkyne and addition of a sulfonyl radical to the resultant vinyl azide. The method enables the stereoselective synthesis of a wide range of β-sulfonyl enamines without electron-withdrawing groups on the nitrogen atom. These enamines are found to be suitable for a variety of further transformations.

摘要

本文报道了银催化的端炔、亚磺酸钠和 TMSN 的分子间氨基磺酰化反应。该三组分反应经历了末端炔烃的顺序氢氮加成反应和磺酰基自由基加成到生成的乙烯基叠氮化物。该方法能够立体选择性地合成一系列氮原子上不带吸电子基团的β-磺酰基烯胺。这些烯胺适合进行多种进一步的转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf6/5655761/0d862d8e38ac/ANIE-56-13805-g001.jpg

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