Zhang Xue, Li Shunian, Yu Wenjing, Xie Yufang, Tung Chen-Ho, Xu Zhenghu
Key Lab for Colloid and Interface Chemistry of Education Ministry, Department of Chemistry, Shandong University, No. 27 South Shanda Road, Jinan 250100, China.
State Key Laboratory of Organometallic Chemistry, Chinese Academy of Sciences, Shanghai 200032, China.
J Am Chem Soc. 2022 Apr 13;144(14):6200-6207. doi: 10.1021/jacs.2c02563. Epub 2022 Apr 4.
An Ir(I)/squaramide cooperative catalytic strategy for atroposelective synthesis of axially chiral aryltriazoles has been developed for the first time. Diverse structurally novel aryltriazole skeletons that cannot be accessed by traditional click reactions were synthesized in good yields with excellent enantioselectivity. Both enantiomers were easily obtained from a pair of diastereoisomeric natural quinidine- and quinine-derived squaramides. A significant Ir(I)/squaramide coordination activation, but no self-quenching phenomenon was observed in this metal/organo cooperative catalytic system.
首次开发了一种用于轴向手性芳基三唑的对映选择性合成的铱(I)/方酰胺协同催化策略。通过传统点击反应无法获得的多种结构新颖的芳基三唑骨架以良好的产率和优异的对映选择性被合成出来。两种对映体都很容易从一对非对映异构的天然奎尼丁和奎宁衍生的方酰胺中获得。在这种金属/有机协同催化体系中观察到显著的铱(I)/方酰胺配位活化,但没有自猝灭现象。