Issue 18, 2018

Electrochemical initiation of electron-catalyzed phenanthridine synthesis by trifluoromethylation of isonitriles

Abstract

The electron-catalyzed formation of phenanthridines starting from isonitriles initiated by an electrochemical reduction of the Togni reagent is presented. The required number of faradays per mole of starting material and the respective yields clearly show the catalytic character of the electron in this reaction. The mechanism is supported by cyclic voltammetry experiments.

Graphical abstract: Electrochemical initiation of electron-catalyzed phenanthridine synthesis by trifluoromethylation of isonitriles

Supplementary files

Article information

Article type
Communication
Submitted
04 Гру 2017
Accepted
03 Січ 2018
First published
12 Лют 2018
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2018,54, 2240-2243

Electrochemical initiation of electron-catalyzed phenanthridine synthesis by trifluoromethylation of isonitriles

M. Lübbesmeyer, D. Leifert, H. Schäfer and A. Studer, Chem. Commun., 2018, 54, 2240 DOI: 10.1039/C7CC09302K

This article is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported Licence. You can use material from this article in other publications, without requesting further permission from the RSC, provided that the correct acknowledgement is given and it is not used for commercial purposes.

To request permission to reproduce material from this article in a commercial publication, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party commercial publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements