通过电-有机催化级联进行不对称环丙烷化反应

IF 4.3 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY Chemical Communications Pub Date : 2024-10-22 DOI:10.1039/d4cc05092d
Anastasiya Krech, Marharyta Laktsevich-Iskryk, Nora Deil, Mihhail Fokin, Mariliis Kimm, Maksim Ošeka
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引用次数: 0

摘要

我们报告了一种通过电催化、碘介导的环闭合,以鎓离子为促进剂不对称合成环丙烷的方法。通过温和、可控的电化学方法生成催化量的亲电碘物种,可防止有机催化剂失活,同时也无需使用卤代试剂,从而简化了传统的合成方法。
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Asymmetric cyclopropanation via electro-organocatalytic cascade
We report an iminium ion-promoted, asymmetric synthesis of cyclopropanes via an electrocatalytic, iodine-mediated ring closure. The mild, controlled electrochemical generation of electrophilic iodine species in catalytic quantities prevents organocatalyst deactivation, while also eliminating the need for halogenated reagents, thus simplifying traditional synthetic approaches.
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来源期刊
Chemical Communications
Chemical Communications 化学-化学综合
CiteScore
8.60
自引率
4.10%
发文量
2705
审稿时长
1.4 months
期刊介绍: ChemComm (Chemical Communications) is renowned as the fastest publisher of articles providing information on new avenues of research, drawn from all the world''s major areas of chemical research.
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