Blasius Clemens K, Heinrich Niklas F, Vasilenko Vladislav, Gade Lutz H
Anorganisch-Chemisches Institut, Universität Heidelberg, Im Neuenheimer Feld 270, 69120, Heidelberg, Germany.
Angew Chem Int Ed Engl. 2020 Sep 7;59(37):15974-15977. doi: 10.1002/anie.202006557. Epub 2020 Jun 25.
A readily activated iron alkyl precatalyst effectively catalyzes the highly enantioselective hydroboration of N-alkyl imines. Employing a chiral bis(oxazolinylmethylidene)isoindoline pincer ligand, the asymmetric reduction of various acyclic N-alkyl imines provided the corresponding α-chiral amines in excellent yields and with up to >99 % ee. The applicability of this base metal catalytic system was further demonstrated with the synthesis of the pharmaceuticals Fendiline and Tecalcet.
一种易于活化的铁烷基预催化剂能有效催化N-烷基亚胺的高度对映选择性硼氢化反应。使用手性双(恶唑啉基亚甲基)异吲哚啉钳形配体,各种无环N-烷基亚胺的不对称还原反应能以优异的产率提供相应的α-手性胺,对映体过量率高达>99%。药物芬地林和特卡塞的合成进一步证明了这种贱金属催化体系的适用性。