96779-70-3

Upstream product

• 71204-44-9 benzyl 2,3-anhydro-4-O-trifluoromethanesulfonyl-α-D-ribopyranoside 

Relevant academic research and scientific papers

Efficient High-Yielding Syntheses and NMR Spectroscopic Studies of Some Fluorodeoxy Sugars

Displacement of the triflyl group by fluoride ion in benzyl 2,3-anhydro-4-O-(trifluoromethylsulfonyl)pyranosides 1-3 leads with stereochemical inversion to the 4-fluoro-4-deoxy sugars 4-6, providing a general method for the introduction of fluorine in the

Epoxide Assisted Displacement of Triflyl Group by Fluoride Ion. An Efficient Approach to Fluorodeoxy Sugars

Displacement of triflyl group by fluoride ion in benzyl 2,3-anhydro sugars leads with stereochemical inversion to fluorodeoxy sugars, providing a general method for the introduction of fluorine in the neighbourhood of oxirane ring in anhydro sugars.This p