Recent progress in asymmetric radical reactions enabled by chiral iron catalysts

被引:1
|
作者
Zhang, Jun [1 ,2 ]
Wu, Jie [1 ,2 ,3 ,4 ,5 ]
机构
[1] Taizhou Univ, Sch Pharmaceut & Chem Engn, 1139 Shifu Ave, Taizhou 318000, Peoples R China
[2] Taizhou Univ, Inst Adv Studies, 1139 Shifu Ave, Taizhou 318000, Peoples R China
[3] Chinese Acad Sci, State Key Lab Organomet Chem, Shanghai Inst Organ Chem, 345 Lingling Rd, Shanghai 200032, Peoples R China
[4] Henan Normal Univ, Sch Chem & Chem Engn, Xinxiang 453007, Peoples R China
[5] Zhejiang Normal Univ, Key Lab Minist Educ Adv Catalysis Mat, Jinhua 321004, Peoples R China
基金
中国国家自然科学基金;
关键词
2-NAPHTHOLS;
D O I
10.1039/d4cc03047h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Transition-metal-catalyzed radical asymmetric reactions offer a versatile and effective platform for accessing chiral organic molecules with high enantiopurity. Given that iron is the most abundant and less toxic transition metalic element available, the application of iron catalysts is considered to be a more sustainable and attractive approach. Over the last decade, several exciting and notable achievements have been witnessed. In this highlight, we aim to provide an overview of the progress in ligand-enabled iron-catalyzed asymmetric radical reactions, with an emphasis on the reaction mechanisms. In this highlight, we discuss recently developed chiral iron catalysts and their application in radical asymmetric reactions for the construction of axial or central chirality.
引用
收藏
页码:12633 / 12649
页数:17
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