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首页> 外文期刊>Organic letters >Single-Electron Transmetalation: Photoredox/Nickel Dual Catalytic Cross-Coupling of Secondary Alkyl beta-Trifluoroboratoketones and -esters with Aryl Bromides
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Single-Electron Transmetalation: Photoredox/Nickel Dual Catalytic Cross-Coupling of Secondary Alkyl beta-Trifluoroboratoketones and -esters with Aryl Bromides

机译:单电子重金属化:仲烷基β-三氟硼酮酮和酯与芳族溴化物的光氧化还原/镍双催化交叉偶联

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摘要

The first cross-coupling of secondary alkyl beta-trifluoroboratoketones and -esters has been achieved through application of photoredoxickel dual catalysis. Although the related beta-trifluoroboratoamides have been effectively cross-coupled via Pd-catalysis, the corresponding ketones and esters had proven recalcitrant prior to this report. Reactions occur under mild conditions, and a variety of functional groups and sterically and electronically diverse reaction partners are tolerated.
机译:仲烷基β-三氟硼烷基酮酸酯与-酯的第一次交叉偶联已通过应用光氧化还原/镍双重催化而实现。尽管相关的β-三氟硼酰胺已通过Pd催化有效地交叉偶联,但在本报告之前,相应的酮和酯已被证明具有顽固性。反应在温和的条件下发生,可以耐受各种官能团以及空间和电子上多样化的反应伙伴。

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