Iridium-Catalyzed Asymmetric Allylic Substitution Reactions

被引:593
作者
Cheng, Qiang [1 ]
Tu, Hang-Fei [1 ]
Zheng, Chao [1 ]
Qu, Jian-Ping [2 ]
Helmchen, Guenter [3 ]
You, Shu-Li [1 ]
机构
[1] Univ Chinese Acad Sci, Chinese Acad Sci, Shanghai Inst Organ Chem, State Key Lab Organometall Chem, 345 Lingling Lu, Shanghai 200032, Peoples R China
[2] Nanjing Tech Univ, Jiangsu Natl Synerget Innovat Ctr Adv Mat, Sch Chem & Mol Engn, Inst Adv Synth, Nanjing 211816, Jiangsu, Peoples R China
[3] Heidelberg Univ, Organ Chem Inst Ruprecht Karls, Neuenheimer Feld 270, D-69120 Heidelberg, Germany
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
HETEROCYCLIC CARBENE COMPLEX; CROSS-COUPLING REACTIONS; ALPHA-AMINO-ACIDS; ENANTIOSELECTIVE MODULAR SYNTHESIS; AMINATION/RING-CLOSING METATHESIS; TETRAHYDRO-BETA-CARBOLINES; IR/ZN DUAL CATALYSIS; STEREOSELECTIVE-SYNTHESIS; DEAROMATIZATION REACTION; PHOSPHORAMIDITE LIGAND;
D O I
10.1021/acs.chemrev.8b00506
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this review, we summarize the origin and advancements of iridium catalyzed asymmetric allylic substitution reactions during the past two decades. Since the first report in 1997, Ir-catalyzed asymmetric allylic substitution reactions have attracted intense attention due to their exceptionally high regio- and enantioselectivities. Ir-catalyzed asymmetric allylic substitution reactions have been significantly developed in recent years in many respects, including ligand development, mechanistic understanding, substrate scope, and application in the synthesis of complex functional molecules. In this review, an explicit outline of ligands, mechanism, scope of nucleophiles, and applications is presented.
引用
收藏
页码:1855 / 1969
页数:115
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