首页> 外文期刊>Organic letters >Combining Ru-Catalyzed C-H Functionalization with Pd-Catalyzed Asymmetric Allylic Alkylation: Synthesis of 3-Allyl-3-aryl Oxindole Derivatives from Aryl alpha-Diazoamides
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Combining Ru-Catalyzed C-H Functionalization with Pd-Catalyzed Asymmetric Allylic Alkylation: Synthesis of 3-Allyl-3-aryl Oxindole Derivatives from Aryl alpha-Diazoamides

机译:结合Ru催化的C-H功能化与Pd催化的不对称烯丙基烷基化:由芳基α-重氮酰胺合成3-烯丙基-3-芳基羟吲哚衍生物

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摘要

Ruthenium-catalyzed C-H functionalization was successfully combined with palladium-catalyzed asymmetric allylic alkylation in one pot. The novel dual-metal-catalyzed reaction provides a variety of 3-allyl-3-aryl oxindoles from the corresponding alpha-diazoamides in up to 99% yield with up to 85% ee. The appropriate ligand choice is important to promote the sequential reaction, avoiding undesired metal interaction or ligand exchange.
机译:在一锅中成功地将钌催化的C-H功能化与钯催化的不对称烯丙基烷基化结合在一起。新颖的双金属催化反应可从相应的α-重氮酰胺中以高达99%的收率和高达85%ee的产率提供各种3-烯丙基-3-芳基羟吲哚。适当的配体选择对于促进顺序反应,避免不希望的金属相互作用或配体交换很重要。

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