化学
亚胺
立体化学
生物催化
组合化学
胺化
分子内力
位阻效应
手性(物理)
氮丙啶
催化作用
立体异构
蛋白质工程
轴手性
酶
还原胺化
定向进化
突变体
立体选择性
分子动力学
动力学分辨率
对映选择合成
人工酶
作者
Zitian Zhou,Yuxuan Yan,Shuai Fan,Zhouchang Yao,Wenbang Wang,Keting Li,Tianzhang Qiao,Ling Huang,Zhaoyong Yang,Haigen Fu
摘要
Atropisomeric dibenz[c,e]azepines are privileged scaffolds in asymmetric synthesis, medicinal chemistry, and materials science, yet their atroposelective preparation remains challenging due to the difficulty of controlling axial chirality while constructing a strained medium-sized ring. Tetra-ortho-substituted dibenz[c,e]azepines are especially elusive, with no catalytic asymmetric method reported owing to extreme steric hindrance. Here, we report the first biocatalytic strategy for the atroposelective synthesis of these congested bridged biaryls, employing an engineered imine reductase (IRED) that catalyzes a sequential inter- and intramolecular reductive amination cascade. Structure-guided directed evolution of an IRED from Streptomyces tricolor provided a triple mutant (IRED-04-M3) that delivers various tetra-ortho-substituted dibenz[c,e]azepines in high yields with excellent atroposelectivity (up to 97% yield, >99:1 er) by dynamic kinetic resolution. Gram-scale preparation was also demonstrated. Mechanistic studies and molecular dynamics simulations provide insight into the cascade reaction and stereocontrol exerted by the engineered enzyme.
科研通智能强力驱动
Strongly Powered by AbleSci AI