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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >Phosphoramidites based on phenyl-substituted 1,2-diols as ligands in palladium-catalyzed asymmetric allylations: the contribution of steric demand and chiral centers to the enantioselectivity
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Phosphoramidites based on phenyl-substituted 1,2-diols as ligands in palladium-catalyzed asymmetric allylations: the contribution of steric demand and chiral centers to the enantioselectivity

机译:钯催化的不对称烯丙基中以苯基取代的1,2-二醇为配体的亚磷酰胺:空间需求和手性中心对对映选择性的贡献

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摘要

A small family of readily available phosphoramidite ligands, including compounds with P*-stereocenters, has been prepared from phenyl-substituted 1,2-diols as simple and cheap starting materials. Using these ligands, up to 84% ee was achieved in Pd-catalyzed asymmetric allylic substitution. The influence of structural modules such as asymmetric atoms and steric demand on the enantioselectivity is discussed.
机译:由苯基取代的1,2-二醇作为简单,廉价的原料,制备了一小撮容易获得的亚磷酰胺配体,包括具有P *-立体中心的化合物。使用这些配体,在Pd催化的不对称烯丙基取代中可实现高达84%ee。讨论了不对称原子和空间需求等结构模块对对映选择性的影响。

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