Electrochemical synthesis of carbazoles by dehydrogenative coupling reaction

Thumbnail Image

Files

kehl_anton-electrochemica-20210705132735420.pdf (964.29 KB)

Date issued

2020

Authors

Editors

Journal Title

Journal ISSN

Volume Title

Publisher

Reuse License

CC-BY-NC-ND-4.0
Description of rights: CC-BY-NC-ND-4.0
Item type: Item , ZeitschriftenaufsatzAccess status: Open Access ,

Abstract

A constant current protocol, employing undivided cells, a remarkably low supporting electrolyte concentration, inexpensive electrode materials, and a straightforward precursor synthesis enabling a novel access to N-protected carbazoles by anodic N,C bond formation using directly generated amidyl radicals is reported. Scalability of the reaction is demonstrated and an easy deblocking of the benzoyl protecting group is presented.

DOI

http://doi.org/10.25358/openscience-6178

Description

Keywords

Citation

URI

https://openscience.ub.uni-mainz.de/handle/20.500.12030/6187

Published in

Chemistry - a European journal, 26, 68, Wiley-VCH, Weinheim, 2020, https://doi.org/10.1002/chem.202003430

Relationships

Collections

JGU-Publikationen

Endorsement

Review

Supplemented By

Referenced By