Issue 79, 2021

Iminyl-radicals by electrochemical decarboxylation of α-imino-oxy acids: construction of indole-fused polycyclics

Abstract

Iminyl radicals are reactive intermediates that can be used for the construction of various valuable heterocycles. Herein, the electrochemical decarboxylation of α-imino-oxy acids for the generation of iminyl radicals has been accomplished under exogenous-oxidant- and metal-free conditions through the use of nBu4NBr as a mediator. The resulting iminyl radicals undergo intramolecular cyclization smoothly with the adjacent (hetero)arenes to afford a series of indole-fused polycyclic compounds.

Graphical abstract: Iminyl-radicals by electrochemical decarboxylation of α-imino-oxy acids: construction of indole-fused polycyclics

Supplementary files

Article information

Article type
Communication
Submitted
19 Jul 2021
Accepted
08 Sep 2021
First published
08 Sep 2021

Chem. Commun., 2021,57, 10242-10245

Iminyl-radicals by electrochemical decarboxylation of α-imino-oxy acids: construction of indole-fused polycyclics

J. Wan, J. Cui, W. Zhong and J. Huang, Chem. Commun., 2021, 57, 10242 DOI: 10.1039/D1CC03891E

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