Direct and selective functionalization of sp³ 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(sp³)–H bonds.

中文翻译：

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协同十杂碳酸盐光-HAT和镍催化实现强C（sp ³）-H芳基化

在有机化合物中无处不在的sp ³ C–H键的直接和选择性官能化仍然是一个长期存在的挑战性反应。在《自然》杂志的最近一篇论文中，麦克米伦及其同事披露，去catungstate的光-HAT与镍催化的合并为强C（sp ³）-H键的直接和选择性芳基化提供了一个温和的，普遍适用的平台。