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首页> 外文期刊>Advanced synthesis & catalysis >Ferrocene-Based Chiral Phosphine-Triazines:A New Family of Highly Efficient P,N Ligands for Asymmetric Catalysis
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Ferrocene-Based Chiral Phosphine-Triazines:A New Family of Highly Efficient P,N Ligands for Asymmetric Catalysis

机译:二茂铁基手性膦-三嗪类化合物:一种新的高效P,N配体,用于不对称催化

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摘要

The presence of the additional heterocyclic nitrogen atoms in chiral P,N ligands has an important influence on the asymmetric catalysis,and a clear trend was observed in the present research that the enantioselectivity and reactivity were significantly increased by raising the number of heterocyclic nitrogen atoms in these P,N ligands.Through finely tuning the number of heterocyclic nitrogen atoms,a new family of ferrocene-based chiral phosphine-triazine ligands with three heterocyclic nitrogen atoms has been developed and successfully applied in Pd-catalyzed asymmetric allylic substitution.Up to 99% ee with 99% yield of allylic alkylation products and 94% ee of allylic animation products have been obtained by the use of ligand(R_c,S_p)-1f with a 4,6-diphenoxy-1,3,5-triazine moiety.
机译:手性P,N配体中额外的杂环氮原子的存在对不对称催化具有重要影响,并且在本研究中观察到明显的趋势是,通过增加杂环氮原子的数目可以大大提高对映选择性和反应性。通过微调杂环氮原子的数目,开发了具有三个杂环氮原子的新的二茂铁基手性膦-三嗪配体家族,并将其成功应用于钯催化的不对称烯丙基取代中。多达99个通过使用具有4,6-二苯氧基-1,3,5-三嗪部分的配体(R_c,S_p)-1f获得了具有99%收率的烯丙基烷基化产物和94%ee收率的%ee。

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