Enantioselective transition metal catalysis directed by chiral cations

被引:32
|
作者
Ye, Xinyi [1 ,2 ]
Tan, Choon-Hong [3 ]
机构
[1] Zhejiang Univ Technol, Coll Pharmaceut Sci, 18 Chaowang Rd, Hangzhou 310014, Peoples R China
[2] Zhejiang Univ Technol, Collaborat Innovat Ctr Yangtze River Delta Reg Gr, 18 Chaowang Rd, Hangzhou 310014, Peoples R China
[3] Nanyang Technol Univ, Div Chem & Biol Chem, 21 Nanyang Link, Singapore 637371, Singapore
关键词
PHASE-TRANSFER; ALLYLIC ALKYLATION; AMINO-ACIDS; OXIDATION; ALLYLATION; COMPLEXES; OXIDANT;
D O I
10.1039/d0sc05734g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Enantioselective transition metal catalysis directed by chiral cations is the amalgamation of chiral cation catalysis and organometallic catalysis. Thus far, three strategies have been revealed: ligand scaffolds incorporated on chiral cations, chiral cations paired with transition metal 'ate'-type complexes, and ligand scaffolds incorporated on achiral anions. Chiral cation ion-pair catalysis has been successfully applied to alkylation, cycloaddition, dihydroxylation, oxohydroxylation, sulfoxidation, epoxidation and C-H borylation. This development represents an effective approach to promote the cooperation between chiral cations and transition metals, increasing the versatility and capability of both these forms of catalysts. In this review, we present current examples of the three strategies and suggest possible inclusions for the future.
引用
收藏
页码:533 / 539
页数:7
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