Journal
ASIAN JOURNAL OF ORGANIC CHEMISTRY
Volume 10, Issue 3, Pages 559-562Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/ajoc.202000650
Keywords
electrolytes; trifluoromethylation; halogenation; 8-aminoquinolines; electrocatalysis
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Funding
- National Natural Science Foundation of China, NSFC [21978273, 21576239]
- National Key R&D Program of China [2018YFC0214100]
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An efficient electrolyte-triggered trifluoromethylation and halogenation at C5 position of 8-aminoquinoline derivatives was developed, giving moderate to excellent yields of C-H functionalization products. The mild and green reactions had lower energy consumption and shorter reaction times, while avoiding the use of transition-metal catalysts and oxidants.
An efficient electrolyte-triggered trifluoromethylation and halogenation at C5 position of 8-aminoquinoline derivatives was developed, affording the C-H functionalization products in moderate to excellent yields. Furthermore, the mild and green reactions had lower energy consumption and shorter times. Most importantly, both transition-metal catalysts and oxidants were avoided.
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