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Coordination-assisted, transition-metal-catalyzed enantioselective desymmetric C-H functionalization
被引:37
|作者:
Yu, Xin
[1
]
Zhang, Zhuo-Zhuo
[2
]
Niu, Jun-Long
[3
]
Shi, Bing-Feng
[1
]
机构:
[1] Zhejiang Univ, Dept Chem, Hangzhou 310027, Zhejiang, Peoples R China
[2] Chengdu Univ, Sch Food & Biol Engn, Chengdu 610106, Sichuan, Peoples R China
[3] Zhengzhou Univ, Coll Chem, Green Catalysis Ctr, Zhengzhou 450001, Peoples R China
基金:
中国博士后科学基金;
关键词:
PLANAR CHIRAL FERROCENES;
C(SP(3))-H BONDS;
ASYMMETRIC-SYNTHESIS;
ALIPHATIC AMIDES;
NATURAL-PRODUCTS;
ACTIVATION;
ARYLATION;
LIGANDS;
BORYLATION;
ALKYLATION;
D O I:
10.1039/d1qo01884a
中图分类号:
O62 [有机化学];
学科分类号:
070303 ;
081704 ;
摘要:
Transition-metal-catalyzed asymmetric C-H functionalization has gradually emerged as a powerful tool for the creation of structural and chiral complexity in an atom- and step-economical fashion. The nature of this strategy provides a variety of methodologies to overcome the limitation of enantioselective desymmetrization caused by the synthesis of preformed multifunctional symmetric substrates. This review aims to summarise recent advances in transition-metal-catalyzed enantioselective desymmetric C-H functionalization reactions via coordination-assisted metal insertion, covering the literature from 2008 to June 2021. The mechanistic pathway and the modes of stereocontrol are discussed where appropriate.
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页码:1458 / 1484
页数:27
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