College of Chemistry and Chemical Engineering, Qingdao University, Ningxia Road 308#, Qingdao, 266071, China.
Angew Chem Int Ed Engl. 2021 Sep 27;60(40):21718-21722. doi: 10.1002/anie.202108747. Epub 2021 Aug 25.
N-C Biaryl atropisomers are prevalent in natural products and bioactive drug molecules. However, the enantioselective synthesis of such molecules has not developed significantly. Particularly, the enantioselective synthesis of N-C biaryl atropisomers by stereoselective metal-catalyzed aryl amination remains unprecedented. Herein, a Pd-catalyzed cross-coupling strategy is presented for the synthesis of N-C axially chiral biaryl molecules. A broad spectrum of N-C axially chiral compounds was obtained with excellent enantioselectivities (up to 99 % ee) and good yields (up to 98 %). The practicality of this reaction was validated in the synthesis of useful biological molecules.
N-C 轴手性联芳化合物在天然产物和生物活性药物分子中很常见。然而,此类分子的对映选择性合成并没有得到显著发展。特别是,通过立体选择性金属催化的芳基胺化反应来对映选择性合成 N-C 轴手性联芳化合物仍是前所未有的。本文提出了一种钯催化的交叉偶联策略,用于合成 N-C 轴手性联芳分子。通过该策略,获得了具有广泛底物适用性的 N-C 轴手性化合物,具有优异的对映选择性(高达 99%ee)和良好的收率(高达 98%)。该反应的实用性已在有用生物分子的合成中得到验证。