Wei Zhikang, Zhao Yi, Wang Tianyi, Li Jiaomeng, Yuan Wei, Wei Liwen, Yang Xing
Key Laboratory of Chemical Biology and Traditional Chinese Medicine (Ministry of Education of China), Key Laboratory of the Assembly and Application of Organic Functional Molecules of Hunan Province College of Chemistry and Chemical Engineering, Hunan Normal University, Changsha 410081, China.
Org Lett. 2024 Aug 30;26(34):7110-7115. doi: 10.1021/acs.orglett.4c02345. Epub 2024 Aug 16.
We disclose herein an asymmetric synthesis of axially chiral oxazepine-containing bridged biaryls via CPA-catalyzed kinetic asymmetric alcoholysis. Control experiments showed that this CPA-catalyzed alcoholysis was reversible, and lowering the reaction temperature could almost suppress the reversible reaction, thus providing a series of axially chiral oxazepine-containing bridged biaryl compounds in good to excellent enantioselectivities. The gram-scale reactions and facile derivatizations of the enantioenriched products demonstrate the practical utility of this reaction.
我们在此披露一种通过CPA催化的动力学不对称醇解反应来不对称合成含氮杂卓的轴手性桥连联芳基化合物的方法。对照实验表明,这种CPA催化的醇解反应是可逆的,降低反应温度几乎可以抑制该可逆反应,从而以良好至优异的对映选择性提供了一系列含氮杂卓的轴手性桥连联芳基化合物。克级规模反应以及对映体富集产物的简便衍生化证明了该反应的实际应用价值。