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  • Nucleophilic addition of potassium alkynyltrifluoroborates to D-glucal mediated by BF3 x OEt2: highly stereoselective synthesis of alpha-C-glycosides.

Nucleophilic addition of potassium alkynyltrifluoroborates to D-glucal mediated by BF3 x OEt2: highly stereoselective synthesis of alpha-C-glycosides.

Organic letters (2008-10-24)
Adriano S Vieira, Pedro F Fiorante, Thomas L S Hough, Fernando P Ferreira, Diogo S Lüdtke, Hélio A Stefani
ABSTRACT

A convenient, mild and highly stereoselective method for C-glycosidation (alkynylation) of D-glucal with various potassium alkynyltrifluoroborates, mediated by BF3x OEt2 and involving oxonium intermediates, preferentially provides the alpha-acetylene glycoside products with good yields.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Boron trifluoride, electronic grade, ≥99.99%
Supelco
Boron trifluoride - 1-butanol solution, ~10% in 1-butanol (∼1.3 M), for GC derivatization, LiChropur
Sigma-Aldrich
Tetrafluoroboric acid solution, 48 wt. % in H2O