757190-34-4Relevant academic research and scientific papers
Boron trifluoride-induced reactions of phenylglycidyl ethers: A convenient synthesis of enantiopure, stereodefined fluorohydrins
Islas-González, Gabriela,Puigjaner, Cristina,Vidal-Ferran, Anton,Moyano, Albert,Riera, Antoni,Pericàs, Miquel A.
, p. 6337 - 6341 (2007/10/03)
Ring-opening hydrofluorination of enantiomerically pure (2S,3S)-3-arylglycidyl ethers (aryl=phenyl, 4-trifluoromethylphenyl) by boron trifluoride-diethyl ether under mild conditions provides β-fluoro alcohols in good yield in a stereospecific manner with
