Journal
RSC ADVANCES
Volume 4, Issue 101, Pages 57923-57928Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c4ra07455f
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Funding
- National Natural Science Foundation of China [21402123, 21202102]
- Zhejiang Provincial Natural Science Foundation of China [LQ14B020001]
- Science Technology Project of Shaoxing City [2013014017]
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Palladium (Pd)-catalyzed desulfitative cross-coupling reactions of sodium arylsulfinates with a wide variety of arylboronic acids were achieved in good to excellent yields under simple aerobic conditions. These catalytic reactions could be accelerated by addition of a catalytic amount of Cu(II) salts as co-catalyst. Moreover, these reactions were tolerant to all of the tested functional groups, making them attractive alternatives to the traditional cross-coupling reactions.
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