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  PhenoFluorMix: Practical Chemoselective Deoxyfluorination of Phenols

Fujimoto, T., & Ritter, T. (2015). PhenoFluorMix: Practical Chemoselective Deoxyfluorination of Phenols. Organic Letters, 17(3), 544-547. doi:10.1021/ol5035518.

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 Creators:
Fujimoto, Teppei1, Author
Ritter, Tobias2, Author           
Affiliations:
1Department of Chemistry and Chemical Biology, Harvard University,s, 12 Oxford Street, Cambridge, Massachusetts 02138, United State, ou_persistent22              
2Research Department Ritter, Max-Planck-Institut für Kohlenforschung, Max Planck Society, Kaiser-Wilhelm-Platz 1, 45470 Mülheim an der Ruhr, DE, ou_2040308              

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Free keywords: PALLADIUM-CATALYZED CONVERSION; COPPER-MEDIATED FLUORINATION; LATE-STAGE FLUORINATION; H BOND FLUORINATION; ARYL FLUORIDES; NUCLEOPHILIC FLUORINATION; REDUCTIVE ELIMINATION; DIARYLIODONIUM SALTS; MEDICINAL CHEMISTRY; BROMIDES
 Abstract: A practical deoxyfluorination with novel deoxyfluorinating reagent PhenoFluorMix, a mixture of N,N'-1,3-bis(2,6-diisopropylphenyl)chloroimidazolium chloride and CsF, is presented. PhenoFluorMix overcomes the challenges associated with hydrolysis of PhenoFluor. PhenoFluorMix does not hydrolyze, is readily available on decagram scale, and is storable in air. In this paper, we demonstrate the practicality of the reagent and exhibit the deoxyfluorination of a variety of phenols and heterocycles.

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Language(s): eng - English
 Dates: 2014-12-092015-01-262015-02-06
 Publication Status: Issued
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/ol5035518
 Degree: -

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Title: Organic Letters
  Other : Org. Lett.
Source Genre: Journal
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Publ. Info: Washington, DC : American Chemical Society
Pages: 4 Volume / Issue: 17 (3) Sequence Number: - Start / End Page: 544 - 547 Identifier: ISSN: 1523-7060
CoNE: https://pure.mpg.de/cone/journals/resource/954925626338