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通过镍环中间体催化羰基化烯-亚胺高效合成多环γ-内酰胺。

Efficient Synthesis of Polycyclic γ-Lactams by Catalytic Carbonylation of Ene-Imines via Nickelacycle Intermediates.

机构信息

Department of Applied Chemistry, Faculty of Engineering, Osaka University, Suita, Osaka, 565-0871, Japan.

Frontier Research Base for Global Young Researchers, Graduate School of Engineering, Osaka University, Suita, Osaka, 565-0871, Japan.

出版信息

Angew Chem Int Ed Engl. 2017 Jul 3;56(28):8206-8210. doi: 10.1002/anie.201703187. Epub 2017 Jun 12.

Abstract

The nickel(0)-catalyzed carbonylative cycloaddition of 1,5- and 1,6-ene-imines with carbon monoxide (CO) is reported. Key to this reaction is the efficient regeneration of the catalytically active nickel(0) species from nickel carbonyl complexes such as [Ni(CO) L]. A variety of tri- and tetracyclic γ-lactams were thus prepared in excellent yields with 100 % atom efficiency. Preliminary results on asymmetric derivatives promise potential in the synthesis of enantioenriched polycyclic γ-lactams.

摘要

报道了镍(0)催化的 1,5-和 1,6-烯亚胺与一氧化碳(CO)的羰基环加成反应。该反应的关键是从镍羰基配合物(如[Ni(CO)L])中有效再生催化活性的镍(0)物种。因此,多种三环和四环γ-内酰胺以优异的收率和 100%的原子效率得到了制备。不对称衍生物的初步结果预示着在手性多环γ-内酰胺合成方面具有潜在应用。

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