Journal
CHEM
Volume 4, Issue 11, Pages 2496-2498Publisher
CELL PRESS
DOI: 10.1016/j.chempr.2018.10.014
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Direct and selective functionalization of sp(3) C-H bonds, which are ubiquitous in organic compounds, remains a long-standing challenging reaction. In a recent paper in Nature, MacMillan and colleagues disclosed that the merger of decatungstate photo-HAT and nickel catalysis provided a mild, generally applicable platform for direct and selective arylation of strong C(sp(3))-H bonds.
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