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首页> 外文期刊>Beilstein journal of organic chemistry. >Copper-catalyzed asymmetric methylation of fluoroalkylated pyruvates with dimethylzinc
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Copper-catalyzed asymmetric methylation of fluoroalkylated pyruvates with dimethylzinc

机译:铜催化的氟烷基丙酮酸与二甲基锌的不对称甲基化

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The catalytic asymmetric methylation of fluoroalkylated pyruvates is shown with dimethylzinc as a methylating reagent in the presence of a copper catalyst bearing a chiral phosphine ligand. This is the first catalytic asymmetric methylation to synthesize various α-fluoroalkylated tertiary alcohols with CF3, CF2H, CF2Br, and n -C n F2 n +1 ( n = 2, 3, 8) groups in good-to-high yields and enantioselectivities. Axial backbones and substituents on phosphorus atoms of chiral phosphine ligands critically influence the enantioselectivity. Moreover, the methylation of simple perfluoroalkylated ketones is found to be facilitated by only chiral phosphines without copper.
机译:在带有手性膦配体的铜催化剂存在下,用二甲基锌作为甲基化试剂显示了氟代烷基化丙酮酸的催化不对称甲基化。这是首次用CF 3 ,CF 2 H,CF 2 Br和n合成各种α-氟烷基化叔醇的催化不对称甲基化反应-C n F 2 n +1 (n = 2,3,8)组-高产率和对映选择性。手性膦配体的磷原子上的轴向骨架和取代基严重影响对映选择性。此外,发现仅通过手性膦而不使用铜可以促进简单的全氟烷基化的酮的甲基化。

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