立体中心
对映选择合成
化学
合成子
环加成
产量(工程)
俘获
组合化学
催化作用
立体化学
有机化学
生态学
生物
冶金
材料科学
作者
Wei Yi,Song Liu,Miaomiao Li,Yi Li,Yu Lan,Liang‐Qiu Lu,Wen‐Jing Xiao
摘要
An enantioselective [5+2] cycloaddition of vinylethylene carbonates and α-diazoketones was achieved for the first time by merging photoactivation and asymmetric Pd catalysis. The key to the success of this method is the enantioselective trapping of Pd-containing, 1,5-dipolar intermediates by ketenes, a class of reactive C2 synthons, which were generated in an in situ and traceless manner under visible light irradiation. Through this trapping, a variety of 7-membered lactones bearing challenging chiral quaternary stereocenters can be accessed in a facile manner with good efficiency and high enantioselectivity (up to 99% yield and 96:4 er).
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