Construction of Planar Chiral Ferrocenes by Cobalt-Catalyzed Enantioselective C-H Acyloxylation Enabled by Dual Ligands

被引:14
|
作者
Huang, Fan-Rui [1 ]
Zhang, Peng [1 ]
Yao, Qi-Jun [1 ]
Shi, Bing-Feng [1 ,2 ]
机构
[1] Zhejiang Univ, Ctr Chem Frontier Technol, Dept Chem, Hangzhou 310027, Peoples R China
[2] Hangzhou Normal Univ, Coll Mat Chem & Chem Engn, Key Lab Organosilicon Chem & Mat Technol, Minist Educ, Hangzhou 311121, Peoples R China
来源
CCS CHEMISTRY | 2023年 / 6卷 / 11期
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
C-H acyloxylation; cobalt; dehydrogena-tive coupling; enantioselectivity; ferrocenes; BOND FUNCTIONALIZATION; DERIVATIVES; OLEFINATION; ACTIVATION; ALKYLATION; INSERTION; ANALOGS; ACCESS; INDOLE;
D O I
10.31635/ccschem.024.202303709
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Oxy-substituted planar chiral ferrocenes are of greatimportance in asymmetric synthesis and pharmaceu-ticals. However, enantioselective C-H activation offerrocenes that form C-O bonds remains a hugechallenge and has not yet been reported. Herein, theasymmetric synthesis of oxy-substituted planar chi-ral ferrocenes is achieved by cobalt-catalyzed enan-tioselective dehydrogenative C-H acyloxylation. Theuse of a dual-ligand system consisting of a chiralsalicyloxazoline (Salox) ligand and a neutral phos-phine oxide ligand, which is oxidized in situ fromthe corresponding phosphine, resulted in good yield(up to 83%) and excellent enantioselectivity (90-99% ee). The utility of this unprecedented pro-tocol is highlighted by its versatile synthetic trans-formations.
引用
收藏
页码:2783 / 2793
页数:11
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