| Literature DB >> 32115957 |
Yongan Liu1, Donghai Yu1, Yong Guo1, Ji-Chang Xiao1, Qing-Yun Chen1, Chao Liu2,1.
Abstract
We report herein a general and practical copper-catalyzed fluorosulfonylation reaction of a wide range of abundant arenediazonium salts to smoothly prepare various arenesulfonyl fluorides using the 1,4-diazabicyclo[2.2.2]octane-bis(sulfur dioxide) adduct as a convenient sulfonyl source in combination with KHF2 as an ideal fluorine source and without the need for additional oxidants. Interestingly, the electronic character of the arene ring in the starting arenediazonium salts has a significant impact on the reaction mechanistic pathway.Entities:
Year: 2020 PMID: 32115957 DOI: 10.1021/acs.orglett.0c00484
Source DB: PubMed Journal: Org Lett ISSN: 1523-7052 Impact factor: 6.005