Issue 15, 2020

Electrifying green synthesis: recent advances in electrochemical annulation reactions

Abstract

Electricity originating from renewable resources can be used for highly sustainable and economically attractive applications. With electrons as the mass-free reagent, the use of a stoichiometric amount of oxidants in annulation reactions can be avoided, thereby eliminating the production of waste. Considered as a modern reaction configuration, the availability of electrochemical methods is expanding synthetic applications in the field of organic chemistry. Electrochemical transformations possess many benefits over traditional reagent-based methodologies, such as high functional group tolerance, mild conditions, easy scale up setup, high yields and selective transformations. In this review, we targeted electrochemical annulation reactions involving mediators and mediator-free conditions with generation of new C–C, C–heteroatom and heteroatom–heteroatom bonds, their mechanistic insights, as well as the reactivity of substrates. We also explain the recent use of sacrificial electrodes in annulation reactions.

Graphical abstract: Electrifying green synthesis: recent advances in electrochemical annulation reactions

Article information

Article type
Tutorial Review
Submitted
15 Apr 2020
Accepted
30 Jun 2020
First published
30 Jun 2020
This article is Open Access
Creative Commons BY-NC license

Green Chem., 2020,22, 4849-4870

Electrifying green synthesis: recent advances in electrochemical annulation reactions

G. M. Martins, G. C. Zimmer, S. R. Mendes and N. Ahmed, Green Chem., 2020, 22, 4849 DOI: 10.1039/D0GC01324B

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