中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Difunctionalization of gem-difluoroalkenes for amination and heteroarylation via metal-free photocatalysis

文献类型:期刊论文

作者Zhong, Yuanchen2,3; Zhuang, Zhen1,2; Zhang, Xiaofei2; Xu, Bin3; Yang, Chunhao1,2
刊名CHEMICAL COMMUNICATIONS
出版日期2024-04-30
卷号60期号:36页码:4830-4833
ISSN号1359-7345
DOI10.1039/d4cc00528g
通讯作者Xu, Bin(xubin@shu.edu.cn) ; Yang, Chunhao(chyang@simm.ac.cn)
英文摘要gem-Difluoroalkenes are widely used building blocks in fluorine chemistry. Herein, a metal-free photocatalytic amination and heteroarylation method of gem-difluoroalkenes with heteroaryl carboxylic acid oxime esters as substrates is reported. This environmentally benign reaction proceeds via radical-radical cross-coupling in energy-transfer-mediated photocatalysis and can be used in the rapid construction of heteroaryl difluoroethylamine scaffolds and late-stage modification of complex pharmaceutical structures.
WOS关键词INHIBITORS ; FLUORINE ; ALKENES
WOS研究方向Chemistry
语种英语
WOS记录号WOS:001202433600001
出版者ROYAL SOC CHEMISTRY
源URL[http://119.78.100.183/handle/2S10ELR8/310753]  
专题新药研究国家重点实验室
通讯作者Xu, Bin; Yang, Chunhao
作者单位1.Univ Chinese Acad Sci, Sch Pharm, 19A Yuquan Rd, Beijing 100049, Peoples R China
2.Chinese Acad Sci, State Key Lab Drug Res, Shanghai Inst Mat Med, 555 Zuchongzhi Rd, Shanghai 201203, Peoples R China
3.Shanghai Univ, Dept Chem, Shanghai 200444, Peoples R China
推荐引用方式
GB/T 7714
Zhong, Yuanchen,Zhuang, Zhen,Zhang, Xiaofei,et al. Difunctionalization of gem-difluoroalkenes for amination and heteroarylation via metal-free photocatalysis[J]. CHEMICAL COMMUNICATIONS,2024,60(36):4830-4833.
APA Zhong, Yuanchen,Zhuang, Zhen,Zhang, Xiaofei,Xu, Bin,&Yang, Chunhao.(2024).Difunctionalization of gem-difluoroalkenes for amination and heteroarylation via metal-free photocatalysis.CHEMICAL COMMUNICATIONS,60(36),4830-4833.
MLA Zhong, Yuanchen,et al."Difunctionalization of gem-difluoroalkenes for amination and heteroarylation via metal-free photocatalysis".CHEMICAL COMMUNICATIONS 60.36(2024):4830-4833.

入库方式: OAI收割

来源:上海药物研究所

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