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首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Copper-Catalyzed Enantioselective Coupling between Allylboronates and Phosphates Using a Phenol-Carbene Chiral Ligand: Asymmetric Synthesis of Chiral Branched 1,5-Dienes
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Copper-Catalyzed Enantioselective Coupling between Allylboronates and Phosphates Using a Phenol-Carbene Chiral Ligand: Asymmetric Synthesis of Chiral Branched 1,5-Dienes

机译:使用苯酚 - 卡宾手性配体与烯丙基酯和磷酸盐之间的铜催化的对映选择性偶联:手性分支的不对称合成1,5-二烯

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摘要

Details of the Cu-catalyzed enantioselective allyl-allyl coupling reaction between allylboronates and (Z)-allylic phosphates using a new chiral N-heterocyclic carbene (NHC) ligand containing a phenolic hydroxy group are presented. The copper catalysis delivers enantioenriched chiral 1,5-dienes with a tertiary stereogenic center. Compatibility with various functional groups and the use of earth-abundant and relatively low-toxicity copper as a metal are attractive features of this protocol. The utility of the chiral phenol-NHC ligand for enantioselective copper catalysis with organoboron compounds is demonstrated and enantiodiscrimination models are discussed.
机译:介绍了使用含有含有酚羟基的新的手性N-杂环(NHC)配体的烯丙基酸盐和(Z)-Allylic磷酸酯之间的Cu催化的母烯醇烯丙基烯丙基酰基偶联反应。 铜催化剂用叔立体中心赋予对母语细胞的手性1,5-二烯。 与各种官能团的兼容性以及作为金属的地球丰富和相对低毒性铜的使用是本协议的有吸引力的特征。 对映选择性铜催化铜催化的手性苯酚-NHC配体的用途证明了有机硼化合物的催化,并讨论了映周性模型。

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