3-Azidoarynes: Generation and Regioselective Reactions

Jumpei Taguchi, Kota Kimura, Kazunobu Igawa, Katsuhiko Tomooka, Takamitsu Hosoya

Research output: Contribution to journalArticlepeer-review

Abstract

The generation of 3-azidoarynes from o-iodoaryl triflatetype precursors was achieved using a silylmethyl Grignard reagent as the activator. The azido group served to control the regioselectivity of the reaction of 3-azidoarynes with arynophiles. The remaining azido group in the adduct also served as a transformable functional group, enabling further derivatization to various nitrogen-containing compounds.

Original languageEnglish
Pages (from-to)94-98
Number of pages5
JournalChemistry Letters
Volume51
Issue number2
DOIs
Publication statusPublished - Feb 2022

All Science Journal Classification (ASJC) codes

  • Chemistry(all)

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