Journal
RSC ADVANCES
Volume 6, Issue 102, Pages 100632-100635Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c6ra22310a
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Funding
- National Natural Science Foundation of China [21502174, 21502175]
- Beijing National Laboratory for Molecular Sciences [20140105]
- Startup Research Fund of Zhengzhou University [1411316005]
- Scientific Research Fund of Henan Provincial Education Department [15A150080]
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A novel strategy for the dearomatization of inactive 1-halonaph-thalenes via palladium-catalyzed reductive Heck-type vinylative reaction was successfully developed. Both homo- and hetero-cyclic naphthalene derivatives were tolerated, and the desired products were obtained in modest to good yields.
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