Recent Advances in Transition-Metal-Catalyzed Enantioconvergent Transformations of Epoxides

被引:0
|
作者
Li, Jianye [1 ]
Li, Sijia [1 ]
Liu, Shuting [2 ]
Cui, Guohao [1 ]
Zhang, Guozhu [1 ]
Guo, Rui [1 ]
机构
[1] Cent China Normal Univ CCNU, Coll Chem, CCNU uOttawa Joint Res Ctr, State Key Lab Green Pesticide,Engn Res Ctr Photoen, 152 Luoyu Rd, Wuhan 430079, Hubei, Peoples R China
[2] Hebei Univ Sci & Technol, Coll Chem & Pharmaceut Engn, Shijiazhuang 050018, Hebei, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
transition-metal-catalyzed; epoxides; enantioconvergent; cross-coupling; functionalization; ASYMMETRIC ALLYLIC AMINATION; MESO-EPOXIDES; KINETIC RESOLUTION; TERMINAL EPOXIDES; COMPLEXES; EFFICIENT; POLYMERIZATION; CONSTRUCTION; ALKYLATION; ALLYLATION;
D O I
10.1055/a-2457-0045
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
In recent years, asymmetric ring-opening reactions of ep-oxides have emerged as a compelling strategy for constructing chiral building blocks in organic synthesis. Among these, transition-metal-catalyzed stereoselective transformations of epoxides have garnered particular attention for their high efficiency and cost-effectiveness. The increasing interest and advancements in this area have spurred exploration into diverse transition-metal catalysts and chiral ligands, highlight-ing their potential to facilitate a wide range of transformations with en-hanced efficiency and flexibility. This short review showcases significantachievements in transition-metal-catalyzed enantioconvergent trans-formations of epoxides, emphasizing their scope of application and re-action mechanisms. 1 Introduction 2 Palladium-Catalyzed Enantioconvergent Cross-Coupling of Epox-ides 3 Nickel-Catalyzed Enantioconvergent Cross-Coupling of Epoxides 4 Titanium-Catalyzed Enantioconvergent Cross-Coupling of Epox-ides 5 Iridium-Catalyzed Enantioconvergent Cross-Coupling of Epox-ides 6 Cobalt-Catalyzed Enantioconvergent Cross-Coupling of Epoxides 7 Copper-Catalyzed Enantioconvergent Cross-Coupling of Epox-ides 8 Conclusions and Outlook
引用
收藏
页数:11
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