化学
铑
试剂
催化作用
芳基
药物化学
有机化学
不对称诱导
对映选择合成
氯化物
烷基
作者
Long Yin,Dewei Zhang,Junhao Xing,Yuhan Wang,Changhui Wu,Tao Lu,Yadong Chen,Tamio Hayashi,Xiaowei Dou
标识
DOI:10.1021/acs.joc.8b00952
摘要
Asymmetric arylation of γ,δ-unsaturated β-ketophosphonates with arylboronic acids is reported. By using the (R)-diene* ligated rhodium(I) chloride complex as a catalyst under none basic conditions, the corresponding β-ketophosphonates bearing a δ-chiral center were obtained in high yields (up to 99%) with good to excellent enantioselectivities (up to >99% ee). The enantioenriched products can be readily converted to diverse chiral β′-aryl enones by the Horner–Wadsworth–Emmons reaction.
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