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Auxiliary-controlled regiodivergent NiH-catalyzed gem-difluoroallylation of alkenyl amines via defluorinative olefin cross-coupling

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成果类型:
期刊论文
作者:
Zhu, Lin;Huang, Jie;Meng, Fanling;Tan, Ziyun;Meng, Xiao;...
通讯作者:
Li, Wenyi;Wang, C
作者机构:
[Zhu, Lin; Wang, C; Wang, Chao; Tan, Ziyun; Li, Wenyi; Li, WY] Hengyang Normal Univ, Coll Chem & Mat Sci, Hengyang 421000, Peoples R China.
[Meng, Fanling; Zhang, Lanlan; Zhu, Lin; Wang, C; Wang, Chao; Huang, Jie; Xiao, Yang; Meng, Xiao] Tianjin Normal Univ, Tianjin Key Lab Struct & Performance Funct Mol, Coll Chem, Tianjin 300387, Peoples R China.
通讯机构:
[Wang, C ; Li, WY] H
Hengyang Normal Univ, Coll Chem & Mat Sci, Hengyang 421000, Peoples R China.
Tianjin Normal Univ, Tianjin Key Lab Struct & Performance Funct Mol, Coll Chem, Tianjin 300387, Peoples R China.
语种:
英文
期刊:
Organic Chemistry Frontiers
ISSN:
2052-4110
年:
2023
卷:
10
期:
22
页码:
5623-5630
基金类别:
This work was supported by the National Natural Science Foundation of China (21901185 and 22002037) and funds provided by Tianjin Normal University. [21901185, 22002037]; National Natural Science Foundation of China; Tianjin Normal University
机构署名:
本校为第一且通讯机构
院系归属:
化学与材料科学学院
摘要:
A NiH-catalyzed migratory and non-migratory gem-difluoroallylation reaction of alkenyl amines with trifluoromethyl alkenes has been developed by judicious choice of directing groups. The reaction incorporates gem-difluoroalkene motifs into aliphatic amine derivatives at multiple positions with high levels of chemo- and regioselectivity. This practical protocol features wide substrate scope, great functional group tolerance, and easy removal of the directing groups. Notably, products from these reactions possess versatile chemical reactivity because of the secondary amide and difluoroalkene fun...

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