Issue 33, 2021

Transition-metal free synthesis of N-aryl carbazoles and their extended analogs

Abstract

Herein, we describe a facile synthesis of N-arylated carbazoles via ladderization of fluorinated oligophenylenes. The reaction consists of two subsequent nucleophilic substitutions triggered by an electronic transfer from dimsyl anions. The reaction allows the effective one-pot formation of at least six C–N bonds with pronounced selectivity to the C–F bond placement.

Graphical abstract: Transition-metal free synthesis of N-aryl carbazoles and their extended analogs

Supplementary files

Article information

Article type
Paper
Submitted
13 May 2021
Accepted
09 Jul 2021
First published
12 Jul 2021

Org. Biomol. Chem., 2021,19, 7172-7175

Transition-metal free synthesis of N-aryl carbazoles and their extended analogs

M. Feofanov, V. Akhmetov, R. Takayama and K. Amsharov, Org. Biomol. Chem., 2021, 19, 7172 DOI: 10.1039/D1OB00940K

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