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Diastereoselective 1,2-difunctionalization of 1,3-enynes enabled by merging photoexcited Hantzsch ester with chromium catalysis

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成果类型:
期刊论文
作者:
Wu, Jia;Xu, Xiangyun;Duan, Chongwen;Chen, Shan;Wang, Dan;...
通讯作者:
Li, FS
作者机构:
[Wu, Jia; Li, Fusheng; Fang, Likui; Duan, Chongwen; Xu, Xiangyun; Wang, Dan; Chen, Shan] Univ South China, Sch Chem & Chem Engn, Hengyang 421001, Peoples R China.
[Tang, Weiyang] Hangzhou Normal Univ, Sch Pharm, Hangzhou 311121, Peoples R China.
通讯机构:
[Li, FS ] U
Univ South China, Sch Chem & Chem Engn, Hengyang 421001, Peoples R China.
语种:
英文
期刊:
Organic Chemistry Frontiers
ISSN:
2052-4110
年:
2024
卷:
11
期:
2
页码:
284-289
基金类别:
We express our gratitude to Dr Weiyang Tang for their valuable suggestions and assistance in conducting the experiments. This work is supported by the Fundamental Research Funds for the University of South China (No. 220XQD08). [220XQD08]; Fundamental Research Funds for the University of South China
机构署名:
本校为第一且通讯机构
院系归属:
化学化工学院
摘要:
1,3-Enynes have been widely recognized as prevalent synthons for the construction of valuable allenes, 1,3-dienes, and propargylic derivatives. However, significant advancements have primarily focused on elucidating the ionic reaction mechanism. The selective difunctionalization of 1,3-enynes involving radicals remains an outstanding challenge in particular within the realm of radical 1,2-difunctionalization. Herein, we present a comprehensive account of the regio- and diastereoselective radical multicomponent 1,2-dialkylation of 1,3-enynes via photoexcited Hantzsch ester and chromium co-catal...

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