4.7 Article

Visible light mediated C-H trifluoromethylation of (hetero)arenes

Journal

ORGANIC CHEMISTRY FRONTIERS
Volume 9, Issue 7, Pages 1982-1985

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2qo00067a

Keywords

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Funding

  1. Students Research Learning and Innovative Experimental Project of University of South China [2020208]
  2. National Key Research and Development Program of China [2021YFF0701700]
  3. National Natural Science Foundation [21971252, 21991122]
  4. Program for Scientific Research Innovation Team in Colleges and Universities of Shandong Province
  5. Jinan Science and Technology Bureau [2019GXRC021]
  6. Key Research Program of Frontier Sciences
  7. Chinese Academy of Sciences (CAS) [QYZDJSSWSLH049]

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A protocol for visible light mediated C-H trifluoromethylation of unactivated (hetero)arenes under blue LED irradiation has been developed. It enables the rapid construction of a range of CF3-containing (hetero)arenes in moderate to high yields from the readily accessible trifluoromethylsulfonyl-pyridinium salt (TFSP). This protocol is also suitable for nitrogen-containing aromatic heterocycles, which are potentially useful in medicinal chemistry.
A protocol for visible light mediated C-H trifluoromethylation of unactivated (hetero)arenes under blue LED irradiation has been developed. The reaction enables the rapid construction of a range of CF3-containing (hetero)arenes in moderate to high yields from the readily accessible trifluoromethylsulfonyl-pyridinium salt (TFSP). This protocol is also suitable for nitrogen-containing aromatic heterocycles, which are potentially useful in medicinal chemistry.

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