立体中心
化学
磷化氢
催化作用
铜
区域选择性
芳基
组合化学
齿合度
配体(生物化学)
反应条件
有机化学
对映选择合成
金属
烷基
受体
生物化学
作者
Wei Li,Cheng Wang,Mengdie Xiao,Li‐Jie Cheng
出处
期刊:Organic Letters
[American Chemical Society]
日期:2024-01-05
卷期号:26 (2): 525-529
被引量:5
标识
DOI:10.1021/acs.orglett.3c03995
摘要
A copper-catalyzed protoarylation of gem-difluoroallenes with aryl boronic esters has been developed, enabling highly regioselective synthesis of gem-difluoroalkenes in high yields. The mild reaction conditions allow for a variety of functional groups to be tolerated, and the reaction can be extended to protoalkenylation of gem-difluoroallenes. The synthetic utility of this method has been demonstrated in gram-scale operation as well as synthesis of chiral gem-difluoroalkenes bearing γ-carbon stereogenic centers in moderate enantioselectivity using a chiral bidentate phosphine ligand with a copper catalyst.
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