Recent Advances in the Synthesis of Chiral Allenes via Asymmetric 1,4-Difunctionalization of 1,3-Enynes

被引:2
|
作者
Li, Sijia [1 ]
Yuan, Kaiyao [1 ]
Zhang, Guozhu [1 ]
Guo, Rui [1 ]
机构
[1] Cent China Normal Univ CCNU, Int Joint Res Ctr Intelligent Biosensing Technol &, CCNU uOttawa Joint Res Ctr, Key Lab Pesticides & Chem Biol,Minist Educ,Coll Ch, 152 Luoyu Rd, Wuhan 430079, Hubei, Peoples R China
基金
中国国家自然科学基金;
关键词
1,4-difunctionalization 1,3-enynes; chiral allenes; transition metal catalysis; asymmetric coupling; OPTICALLY-ACTIVE ALLENES; ENANTIOSELECTIVE SYNTHESIS; TRISUBSTITUTED ALLENES; PROPARGYLIC PHOSPHATES; EFFICIENT SYNTHESIS; KINETIC RESOLUTION; ALLENOATES; HYDROSILYLATION; 2,3-ALLENOATES; 1-BUTEN-3-YNES;
D O I
10.1002/ejoc.202301316
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Allenes represent a distinctive class of organic molecules characterized by their unique physical and chemical properties. Among them, chiral allenes play a significant role in modern chemistry. They not only serve as pivotal frameworks for natural products and drug molecules but also are essential building blocks in organic synthesis. Over the years, numerous remarkable and efficient methods have been developed for the synthesis of chiral allenes. Notably, the catalytic synthesis of chiral allenes using transition metals in conjunction with chiral ligands has garnered considerable attention. This review paper aims to provide an overview of recent advancements in the synthesis of chiral allenes through asymmetric 1,4-difunctionalization of 1,3-enynes, in which two distinct strategies including non-radical and radical processes are highlighted. This review presents an overview of recent advancements in the synthesis of chiral allenes through asymmetric 1,4-difunctionalization of 1,3-enynes, in which two distinct strategies including non-radical and radical processes are highlighted, aiming to provide valuable insights and ideas for further studies in this field. image
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页数:15
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