Facile access to ?-hydroxyl ketones via a cobalt-catalyzed ring-opening/hydroxylation cascade of cyclopropanols

被引:5
|
作者
Zhai, Shengxian [1 ]
Qiu, Shuxian [2 ]
Yang, Shuangtao [1 ]
Gao, Xingyuan [2 ]
Feng, Xinyu [1 ]
Yun, Chenzhe [1 ]
Han, Ning [1 ]
Niu, Yongsheng [1 ]
Wang, Jing [1 ]
Zhai, Hongbin [3 ,4 ,5 ,6 ]
机构
[1] Anyang Inst Technol, Coll Chem & Environm Engn, Anyang 455000, Peoples R China
[2] Guangdong Univ Educ, Engn Technol Dev Ctr Adv Mat & Energy Saving Emiss, Guangzhou 510303, Peoples R China
[3] Peking Univ, State Key Lab Chem Oncogen, Shenzhen Grad Sch, Shenzhen 518055, Peoples R China
[4] Peking Univ, Key Lab Chem Genom, Shenzhen Engn Lab Nano Drug Slow Release, Shenzhen Grad Sch, Shenzhen 518055, Peoples R China
[5] Shenzhen Bay Lab, Shenzhen 518055, Peoples R China
[6] Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
Cobalt catalysis; Ring-opening; Cyclopropanol; -Hydroxy ketone; Cascade reaction; C BOND-CLEAVAGE; EFFICIENT SYNTHESIS; H ACTIVATION; VINYL AZIDES; BETA; STRATEGY; FUNCTIONALIZATION; CHEMISTRY; TRIFLUOROMETHYLATION; FLUORINATION;
D O I
10.1016/j.cclet.2022.06.080
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A cobalt-catalyzed ring-opening/hydroxylation cascade of highly strained cyclopropanols has been developed for the first time. The reaction was conducted under open-air atmosphere to afford a broad series of structurally diverse /3-hydroxy ketones in moderate to good yields with high regioselectivity. The protocol features mild reaction conditions, simple operation, high-functional-group tolerance, facile scalability, and heterocycle compatibility.(c) 2023 Published by Elsevier B.V. on behalf of Chinese Chemical Society and Institute of Materia Medica, Chinese Academy of Medical Sciences.
引用
收藏
页数:4
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