Equipe Chimie Moléculaire Organique, LCP UMR 6264, Boite 562, Université Paul Cézanne, Faculté des Sciences St Jérôme, Avenue Escadrille Normandie-Niemen, 13397, Marseille Cedex 20, France.
Org Biomol Chem. 2010 Sep 21;8(18):4165-8. doi: 10.1039/c0ob00054j. Epub 2010 Jul 27.
Chemoenzymatic dynamic kinetic resolution (DKR) of amines involving sulfanyl radical-induced racemization happened to be the very first switchable DKR process allowing the synthesis of either (R)- or (S)-amides, in good yield and high enantiomeric excess, depending on the nature of the enzyme; the different steps of the development of (S)-selective DKR are discussed.
涉及硫自由基诱导外消旋化的手性胺的酶促动态动力学拆分(DKR)正好是第一个可切换的 DKR 过程,可根据酶的性质以良好的收率和高对映体过量合成(R)-或(S)-酰胺;讨论了(S)-选择性 DKR 发展的不同步骤。