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
Hauptverfasser: Yang, Chun-Hua, Chen, Xixi, Li, Huimin, Wei, Wenbo, Yang, Zhantao, Chang, Junbiao
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Sprache:eng
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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.
ISSN:1359-7345
1364-548X
DOI:10.1039/c8cc04262d