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钯催化、降冰片烯介导、邻位氨基化反位酰胺化:顺序 C-N 键形成。

Palladium-Catalyzed, Norbornene-Mediated, ortho-Amination ipso-Amidation: Sequential C-N Bond Formation.

机构信息

Davenport Research Laboratories, Department of Chemistry, University of Toronto , Toronto M5S 3H6, Canada.

出版信息

Org Lett. 2018 Jan 19;20(2):345-348. doi: 10.1021/acs.orglett.7b03577. Epub 2017 Dec 28.

Abstract

A palladium-catalyzed, norbornene-mediated ortho- and ipso-C-N bond-forming Catellani reaction is reported. This reaction proceeds through a sequential intermolecular amination followed by intramolecular cyclization of a tethered amide. The products, ortho-aminated dihydroquinolinones, were generated in moderate to good yields and are present in bioactive molecules. This work highlights the challenge of competing intra- vs intermolecular palladium-catalyzed processes.

摘要

报道了钯催化、降冰片烯介导的邻位和同碳 C-N 键形成的 Catellani 反应。该反应通过连接酰胺的分子间氨化 followed by 分子内环化进行。邻位氨化的二氢喹啉酮以中等至良好的收率生成,存在于生物活性分子中。这项工作强调了竞争的分子内与分子间钯催化过程的挑战。

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