Fluorination at C2', C3' and C5' of nucleosides with 1-chloromethyl-4-fluoro-1,4-diazabicyclo[2.2.2]octane bis(tetrafluoroborate) SELECTFLUOR(TM) reagent

Article abstract of DOI:10.1080/00397919508011410

Electrophilic fluorination of thioaryl ethers on the sugar component of nucleosides with commercially available SELECTFLUOR(TM) reagent provides a new method for the synthesis of C2', C3' and C5' fluoronucleosides.

Full text of DOI:10.1080/00397919508011410

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Fluorination at C2′, C3′ and
C5′ of Nucleosides with 1-
Chloromethyl-4-fluoro-1,4-
diazabicyclo[2.2.2]octane
bis(Tetrafluoroborate)
SelectfluorTM Reagent
G. Sankar Lal a
a Corporate Science and Technology Center, Air
Products and Chemicals, Inc. , 7201, Hamilton
Boulevard, Allentown, PA, 18195-1501
Published online: 23 Sep 2006.
To cite this article: G. Sankar Lal (1995) Fluorination at C2′, C3′ and C5′
of Nucleosides with 1-Chloromethyl-4-fluoro-1,4-diazabicyclo[2.2.2]octane
bis(Tetrafluoroborate) SelectfluorTM Reagent, Synthetic Communications: An
International Journal for Rapid Communication of Synthetic Organic Chemistry,
25:5, 725-737
To link to this article: http://dx.doi.org/10.1080/00397919508011410
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