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.
- This article is part of the themed collection: Synthetic methodology in OBC