Max-Planck-Institut für Kohlenforschung, Kaiser-Wilhelm-Platz 1, 45470, Mülheim an der Ruhr, Germany.
Angew Chem Int Ed Engl. 2019 Aug 12;58(33):11479-11482. doi: 10.1002/anie.201905623. Epub 2019 Jul 12.
We report a highly enantioselective catalytic protonation of bis-silyl ketene acetals. Our method delivers α-branched carboxylic acids, including nonsteroidal anti-inflammatory arylpropionic acids such as Ibuprofen, in high enantiomeric purity and high yields. The process can be incorporated in an overall deracemization of α-branched carboxylic acids, involving a double deprotonation and silylation followed by the catalytic asymmetric protonation.
我们报告了一种对双硅基烯酮缩醛的高对映选择性催化质子化反应。我们的方法提供了α-支链羧酸,包括非甾体抗炎药芳基丙酸如布洛芬,具有高对映体纯度和高收率。该过程可以整合到α-支链羧酸的整体外消旋化中,涉及双重去质子化和硅化,然后进行催化不对称质子化。