Asymmetric cyclopropanation via an electro-organocatalytic cascade

Abstract

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 halogenating reagents, thus simplifying traditional synthetic approaches.

Graphical abstract: Asymmetric cyclopropanation via an electro-organocatalytic cascade

Supplementary files

Article information

Article type
Communication
Submitted
29 Sept. 2024
Accepted
21 Okt. 2024
First published
22 Okt. 2024
This article is Open Access
Creative Commons BY license

Chem. Commun., 2024, Advance Article

Asymmetric cyclopropanation via an electro-organocatalytic cascade

A. Krech, M. Laktsevich-Iskryk, N. Deil, M. Fokin, M. Kimm and M. Ošeka, Chem. Commun., 2024, Advance Article , DOI: 10.1039/D4CC05092D

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