首页> 美国卫生研究院文献>Molecules >Spiro Indane-Based Phosphine-Oxazolines as Highly Efficient PN Ligands for Enantioselective Pd-Catalyzed Allylic Alkylation of Indoles and Allylic Etherification
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Spiro Indane-Based Phosphine-Oxazolines as Highly Efficient PN Ligands for Enantioselective Pd-Catalyzed Allylic Alkylation of Indoles and Allylic Etherification

机译:基于螺茚满的膦-恶唑啉作为高效PN配体用于对映选择性Pd催化的吲哚烯丙基烷基化和烯丙基醚化

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摘要

A series of indane-based phosphine-oxazoline ligands with a spirocarbon stereogenic center were examined for palladium-catalyzed asymmetric allylic alkylation of indoles. Under optimized conditions, high yields (up to 98%) and enantioselectivities (up to 98% ee) were obtained with a broad scope of indole derivatives. The ligand was determined to be the most efficient P,N-ligand for this reaction. Moreover, the ligand was also efficient for Pd-catalyzed asymmetric allylic etherification with hard aliphatic alcohols as nucleophiles.
机译:研究了一系列具有螺碳立体异构中心的基于茚满的膦-恶唑啉配体的钯催化吲哚的不对称烯丙基烷基化反应。在优化的条件下,使用多种吲哚衍生物可获得高收率(最高98%)和对映选择性(最高98%ee)。确定该配体是该反应最有效的P,N-配体。而且,该配体对于以硬脂族醇作为亲核试剂的钯催化的不对称烯丙基醚化反应也是有效的。

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