Journal
CHEMICAL COMMUNICATIONS
Volume 49, Issue 68, Pages 7501-7503Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c3cc43723j
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Funding
- National Natural Science Foundation of China [21172185]
- Hunan Provincial Natural Science Foundation of China [11JJ1003, 12JJ7002]
- New Century Excellent Talents in University from Ministry of Education of China [NCET-11-0974]
- Hunan Provincial Innovative Foundation for Postgraduate [CX2012B250]
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A palladium-catalyzed desulfitative hydroarylation of alkynes with aryl sulfinic acid sodium salts is described. The reaction showed good regio- and stereoselectivity, and afforded the hydroarylation products in good yields. Various functional groups were well tolerated under the optimized reaction conditions.
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