Journal
CHEMISTRYSELECT
Volume 2, Issue 1, Pages 428-431Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/slct.201601549
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Funding
- National Natural Science Foundation of China [21502160, 21372187, 21572194]
- Project Supported by Scientific Research Fund of Hunan Provincial Education Department [15C1311, YB2016B024]
- China Postdoctoral Science Foundation Funded Project [2015 M572257]
- Hunan Provincial Natural Science Foundation of China [16JJ3112]
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An efficient and convenient method has been developed for the preparation of aryl sulfides via a piperidine promoted direct sulfenylation of naphthols with arylthiols under aqueous conditions. This synthetic strategy features environmental friendliness, easy operation, and mild reaction conditions.
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