Iodine catalyzed reduction of quinolines under mild reaction conditions
A reduction of quinolines to synthetically versatile tetrahydroquinoline molecules with I and HBpin is described. In the presence of iodine (20 mol%) as a catalyst, reduction of quinolines and other N-heteroarenes proceeded readily with hydroboranes as the reducing reagents. The broad functional-gro...
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Veröffentlicht in: | Chemical communications (Cambridge, England) England), 2018-08, Vol.54 (62), p.8622-8625 |
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Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
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Online-Zugang: | Volltext |
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Zusammenfassung: | A reduction of quinolines to synthetically versatile tetrahydroquinoline molecules with I
and HBpin is described. In the presence of iodine (20 mol%) as a catalyst, reduction of quinolines and other N-heteroarenes proceeded readily with hydroboranes as the reducing reagents. The broad functional-group tolerance, good yields and mild reaction conditions imply high practical utility. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c8cc04262d |