@article{2e0bb2dc47734e4abf0985b354a15db1,
title = "Highly β-stereoselective glycosylation by use of 1-O-acetyl-2,6-anhydro-2-thio glycosyl donor for synthesis of 2,6-dideoxy-β-glycosides",
abstract = "Gycosylations of the 1-O-acetyl-2,6-anhydro-2-thio sugar 3 with alcohols in the presence of several Lewis acids in CH2Cl2 proceeded smoothly to give the corresponding β-O-glycosides with high stereocontrol in high yields, and the selectivity of the glycosylation was highly independent on Lewis acids.",
keywords = "1-O-acetyl-2,6-anhydro-2-thio glycosyl donor, 2,6-dideoxy glycoside, Lewis acid, thermodynamic control, β-stereoselective glycosylation",
author = "Kazunobu Toshima and Yuko Nozaki and Satsuki Mukaiyama and Kuniaki Tatsuta",
note = "Funding Information: We are grateful to the Instituteo f Microbial Chemistry for the generouss upporto f our program.F inancial supports by the Ministry of Education, Science and Culture (Grant-in-Aid Scientific Research) is gratefully acknowledged.",
year = "1992",
month = mar,
day = "10",
doi = "10.1016/S0040-4039(00)91656-3",
language = "English",
volume = "33",
pages = "1491--1494",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "11",
}