Article ; Online: 1,2-Fluorosulfenylation of unactivated alkenes with thiols and a fluoride source promoted by bromodimethylsulfonium bromide.
Chemical communications (Cambridge, England)
2023 Volume 59, Issue 95, Page(s) 14153–14156
Abstract: A practical method that enables the fluorosulfenylation of unactivated alkenes processed directly with thiols and fluoride salts is presented. Good to excellent efficiencies and functional group tolerance are observed for both alkene substrates and ... ...
Abstract | A practical method that enables the fluorosulfenylation of unactivated alkenes processed directly with thiols and fluoride salts is presented. Good to excellent efficiencies and functional group tolerance are observed for both alkene substrates and thiols. The procedure also allows the use of gaseous ethylene as a two-carbon building block for β-fluoro thioether products. |
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Language | English |
Publishing date | 2023-11-28 |
Publishing country | England |
Document type | Journal Article |
ZDB-ID | 1472881-3 |
ISSN | 1364-548X ; 1359-7345 ; 0009-241X |
ISSN (online) | 1364-548X |
ISSN | 1359-7345 ; 0009-241X |
DOI | 10.1039/d3cc05045a |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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