@article{oai:nagasaki-u.repo.nii.ac.jp:00001994,
 author = {Makura, Yui and Ueda, Atsushi and Matsuzaki, Takashi and Minamino, Tetsuo and Tanaka, Masakazu},
 issue = {27},
 journal = {Tetrahedron},
 month = {May},
 note = {An α-selective glycosidation reaction of D-tagatofuranose was successfully achieved using 3,4-O-isopropylidene-protected D-tagatofuranose as a glycosyl donor. A variety of glycosyl acceptors, including primary, secondary, and β-amino alcohols, and carbohydrates, can be used for this D-tagatofuranosidation reaction with complete α-selectivities and good yields (57-83%). The stereochemistries at the anomeric positions were determined by nuclear Overhauser effect spectroscopic correlations, as well as comparison of the chemical shifts in the 13C NMR spectra., Tetrahedron, 75(27), pp.3758-3766; 2019},
 pages = {3758--3766},
 title = {α-Selective glycosidation of d-tagatofuranose with a 3,4-O-isopropylidene protection},
 volume = {75},
 year = {2019}
}