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  PhenoFluor: Practical Synthesis, New Formulation, and Deoxyfluorination of Heteroaromatics

Fujimoto, T., Becker, F., & Ritter, T. (2014). PhenoFluor: Practical Synthesis, New Formulation, and Deoxyfluorination of Heteroaromatics. Organic Process Research & Development, 18(8), 1041-1044. doi:10.1021/op500121w.

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Item Permalink: https://hdl.handle.net/11858/00-001M-0000-002B-8597-A Version Permalink: https://hdl.handle.net/21.11116/0000-0000-F69D-A
Genre: Journal Article

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 Creators:
Fujimoto, Teppei1, Author
Becker, Fabian1, Author
Ritter, Tobias1, Author           
Affiliations:
1Harvard Univ, Dept Chem & Chem Bio, , 12 Oxford St, Cambridge, MA 02138 USA., ou_persistent22              

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Free keywords: COPPER-MEDIATED FLUORINATION; ARYL FLUORIDES; CATALYZED FLUORINATION; NUCLEOPHILIC FLUORINATION; REDUCTIVE ELIMINATION; FUNCTIONALIZED ARYL; BOND FORMATION; CONVERSION; STANNANES; ALCOHOLS
 Abstract: We report a practical synthesis method of the reagent PhenoFluor on decagram scale, provide a new formulation of PhenoFluor as a toluene solution, which should decrease challenges associated with the moisture sensitivity of the reagent, and expand the substrate scope of deoxyfluorination with PhenoFluor to heteroaromatics.

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Language(s): eng - English
 Dates: 2014-04-132014-07-232014-08-15
 Publication Status: Issued
 Pages: 4
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1021/op500121w
 Degree: -

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Title: Organic Process Research & Development
  Other : Org. Process Res. Dev.
Source Genre: Journal
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Affiliations:
Publ. Info: Washington, DC : American Chemical Society
Pages: 4 Volume / Issue: 18 (8) Sequence Number: - Start / End Page: 1041 - 1044 Identifier: ISSN: 1083-6160
CoNE: https://pure.mpg.de/cone/journals/resource/1083-6160