Iridium Catalysed Asymmetric Allylic Substitution Reaction of Indolizine Derivatives

被引:16
作者
Lu, Jiamin [1 ]
Wang, Meifang [1 ]
Xu, Ruigang [1 ]
Sun, Haizhou [1 ]
Zheng, Xuan [1 ]
Zhong, Guofu [1 ]
Zeng, Xiaofei [1 ]
机构
[1] Hangzhou Normal Univ, Coll Mat Chem & Chem Engn, 2318 Yuhangtang Rd, Hangzhou 311121, Peoples R China
基金
中国国家自然科学基金;
关键词
Iridium catalysis; Indolizine; Allylic substitution; Asymmetric synthesis; C3; FUNCTIONALIZATION; N-ALLYLATION; CONSTRUCTION; ARYLATION; ALCOHOLS; NITROGEN; OXYGEN;
D O I
10.1002/ajoc.202100171
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A highly efficient direct asymmetric allylic substitution (AAS) reaction of indolizine derivatives with allylic alcohols for accessing enantioenriched indolizine derivatives was realized by combining a chiral iridium complex catalyst with Lewis acid under mild reaction conditions, delivering various chiral allylation products in remarkably high yields and excellent enantioselectivities. This protocol distinguishes itself by availability of the starting materials, mild reaction conditions, broad substrate scope, high yields, excellent selectivity and easy scale-up in a stereoselective manner, which provides a highly efficient protocol for chiral indolizines.
引用
收藏
页码:1500 / 1507
页数:8
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