757190-35-5Relevant academic research and scientific papers
Boron trifluoride-induced, new stereospecific rearrangements of chiral epoxy ethers. Ready access to enantiopure 4-(diarylmethyl)-1,3-dioxolanes and 4,5-disubstituted tetrahydrobenzo[c]oxepin-4-ols
Islas-Gonzalez, Gabriela,Benet-Buchholz, Jordi,Maestro, Miguel A.,Riera, Antoni,Pericas, Miquel A.
, p. 1537 - 1544 (2007/10/03)
Upon treatment with BF3 · Et2O at low temperature, enantiopure benzyl-type ethers of arylglycidols with electron withdrawing substituents at the skeletal aryl group and electron donating substituents at the benzyl group undergo stere
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
