Asymmetric synthesis of allylic compounds via hydrofunctionalisation and difunctionalisation of dienes, allenes, and alkynes

被引:316
作者
Li, Guanlin [1 ]
Huo, Xiaohong [1 ]
Jiang, Xieyang [1 ]
Zhang, Wanbin [1 ,2 ,3 ]
机构
[1] Shanghai Jiao Tong Univ, Shanghai Key Lab Mol Engn Chiral Drugs, Sch Chem & Chem Engn, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
[2] Shanghai Jiao Tong Univ, Sch Pharm, 800 Dongchuan Rd, Shanghai 200240, Peoples R China
[3] Zhengzhou Univ, Coll Chem & Mol Engn, 75 Daxue Rd, Zhengzhou 450052, Peoples R China
基金
中国国家自然科学基金;
关键词
FUNCTIONALLY-SUBSTITUTED ARYL; RHODIUM-CATALYZED ALLYLATION; REGIOSELECTIVE DECARBOXYLATIVE ADDITION; OPTICALLY-ACTIVE ALLYLSILANES; SYNERGISTIC CU/PD CATALYSIS; DIELS-ALDER REACTION; ALPHA-AMINO-ACIDS; H BOND ACTIVATION; ENANTIOSELECTIVE SYNTHESIS; CONJUGATED DIENES;
D O I
10.1039/c9cs00400a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydrofunctionalisation and difunctionalisation of dienes, allenes, and alkynes are widely utilized in the synthesis of valuable allylic compounds. In the past decades, asymmetric catalysis has emerged as one of the most attractive fields in organic synthesis. Recently, the asymmetric versions of hydro-functionalisation and difunctionalisation reactions have become powerful and compelling tools to afford enantiopure allylic compounds, appealing to a large range of chemists. Various metal complexes modified with a large number of chiral ligands and several chiral organocatalysts have been developed to promote the hydrofunctionalisation and difunctionalisation reactions and expand substrate scope. This review provides an overview of this field, and aims at summarizing the chiral ligand used in this area of research. A detailed discussion of the development of these reactions and the general reaction mechanisms is provided.
引用
收藏
页码:2060 / 2118
页数:59
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