Wen Hao-Chen, Chen Wei, Li Meng, Ma Chen, Wang Jian-Fei, Fu Aiping, Xu Shi-Qi, Zhou Yi-Feng, Ni Shao-Fei, Mao Bin
Collaborative Innovation Center of Yangtze River Delta Region Green Pharmaceuticals, Zhejiang University of Technology, Hangzhou, P.R. China.
Department of Chemistry and Key Laboratory for Preparation and Application of Ordered Structural Materials of Guangdong Province, Shantou University, Shantou, China.
Nat Commun. 2024 Jun 20;15(1):5277. doi: 10.1038/s41467-024-49435-2.
The synthesis of chiral α-azaheteroaryl oxiranes via enantioselective catalysis is a formidable challenge due to the required complex stereoselectivity and diverse N-heterocyclic structures. These compounds play a crucial role in developing bioactive molecules, where precise chirality significantly influences biological activity. Here we show that using chiral phosphoric acid as a catalyst, our method efficiently addresses these challenges. This technique not only achieves high enantio- and diastereoselectivity but also demonstrates superior chemo- and stereocontrol during the epoxidation of alkenyl aza-heteroarenes. Our approach leverages a synergistic blend of electrostatic and hydrogen-bonding interactions, enabling the effective activation of both substrates and hydrogen peroxide. The resulting chiral oxiranes exhibit enhanced diversity and functionality, aiding the construction of complex chiral azaaryl compounds with contiguous stereocenters. Kinetic and density functional theory studies elucidate the mechanism, highlighting chiral phosphoric acid's pivotal role in this intricate enantioselective process.
由于所需的复杂立体选择性和多样的N-杂环结构,通过对映选择性催化合成手性α-氮杂芳基环氧乙烷是一项艰巨的挑战。这些化合物在生物活性分子的开发中起着至关重要的作用,其中精确的手性显著影响生物活性。在这里,我们表明,使用手性磷酸作为催化剂,我们的方法有效地应对了这些挑战。该技术不仅实现了高对映选择性和非对映选择性,而且在烯基氮杂芳烃的环氧化过程中表现出卓越的化学和立体控制。我们的方法利用了静电和氢键相互作用的协同组合,能够有效激活底物和过氧化氢。所得的手性环氧乙烷表现出增强的多样性和功能性,有助于构建具有连续立体中心的复杂手性氮杂芳基化合物。动力学和密度泛函理论研究阐明了该机制,突出了手性磷酸在这一复杂的对映选择性过程中的关键作用。