Journal
ORGANIC CHEMISTRY FRONTIERS
Volume 8, Issue 7, Pages 1490-1495Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/d0qo01651a
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Funding
- Hubei Technological Innovation Project [2019ACA125]
- Science, Technology and Innovation Commission of Shenzhen Municipality [JCYJ20180305180832515]
- Fundamental Research Funds for the Central Universities [HUST: 2020kfyXJJS062]
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An efficient iron-catalyzed cross-dehydrogenative aromatic C-H amidation using DDQ as an oxidant under mild conditions is reported, providing a straightforward access to structurally diverse diarylamine derivatives incorporating benzofuran/benzothiophene motifs. Mechanistic studies indicated that a nitrogen-centered anilino radical is involved in the C-N bond formation.
An efficient iron-catalyzed cross-dehydrogenative aromatic C-H amidation using DDQ as an oxidant under mild conditions is reported, providing a straightforward access to structurally diverse diarylamine derivatives incorporating benzofuran/benzothiophene motifs. Mechanistic studies indicated that a nitrogen-centered anilino radical is involved in the C-N bond formation.
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