Boron Trifluoride-Catalyzed Rearrangement of 2-Aryloxytetrahydropyrans: A New Entry to C-Arylglycosidation

DOI: 10.1055/s-1988-27788

Source and publish data:

Synthesis p. 1005 - 1007 (1988)

Update date:2022-08-02

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Authors:

Kometani, Tadashi

Kondo, Hiroyuki

Fujimori, Yukio

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Article abstract of DOI:10.1055/s-1988-27788

Treatment of 2-aryloxytetrahydropyrans with boron trifluoride afforded 2-aryltetrahydropyrans via rearrangement in good yield.Aryl O-glycopyranosides were converted into the corresponding C-glycopyranosides by the same procedure.

Full text of DOI:10.1055/s-1988-27788

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