Redox-Neutral electrochemical Diazo Coupling: Controlled Synthesis of Olefins and Azines via modulating reaction conditions

Abstract

We report a metal-free, linear paired redox-neutral electrochemical diazo coupling that enables the controllable synthesis of olefins and azines by modulating reaction conditions. The protocol exhibits a broad substrate scope, delivering desired products in good yields and diastereoselectivities. Mechanistic investigations, including control experiments and cyclic voltammetry studies, support a cathodically initiated radical-anion formation pathway.

Supplementary files

Article information

Article type
Research Article
Submitted
14 Apr 2026
Accepted
05 Jun 2026
First published
06 Jun 2026
This article is Open Access
Creative Commons BY-NC license

Org. Chem. Front., 2026, Accepted Manuscript

Redox-Neutral electrochemical Diazo Coupling: Controlled Synthesis of Olefins and Azines via modulating reaction conditions

A. Mohapatra and V. Tyagi, Org. Chem. Front., 2026, Accepted Manuscript , DOI: 10.1039/D6QO00499G

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