@article{84a9e0c6fc5e489c95704f635cc0fc40,
title = "Environmentally benign and stereoselective formation of β-mannosidic linkages utilizing 2,3-di-O-benzyl-4,6-O-benzylidene-protected mannopyranosyl phosphite and montmorillonite K-10",
abstract = "An environmentally benign and stereoselective β-mannopyranosylation has been developed employing 4,6-O-benzylidene-protected mannopyranosyl diethyl phosphite as a glycosyl donor and montmorillonite K-10 as an activator.",
keywords = "Glycosidation, Glycosyl phosphite, Montmorillonite K-10, Solid acid, β-Mannopyranoside",
author = "Hideyuki Nagai and Shuichi Matsumura and Kazunobu Toshima",
note = "Funding Information: This research was partially supported by Grant-in-Aid for the 21st Century COE program {\textquoteleft}KEIO Life Conjugate Chemistry{\textquoteright} from the Ministry of Education, Culture, Sports, Science, and Technology, Japan.",
year = "2003",
month = jul,
day = "22",
doi = "10.1016/S0008-6215(03)00234-9",
language = "English",
volume = "338",
pages = "1531--1534",
journal = "Carbohydrate Research",
issn = "0008-6215",
publisher = "Elsevier BV",
number = "15",
}