@article{efe1a50fa4df4260ac5cc9d271415512,
title = "Aryl C-glycosylation using an ionic liquid containing a protic acid",
abstract = "Aryl C-glycosylation of several glycosyl donors, including unprotected sugars, with phenol and naphthol derivatives in an ionic liquid containing a protic acid proceeded effectively and stereoselectively to give the corresponding aryl C-glycosides in good to high yields. Because the ionic liquid was nonvolatile, the reaction could be carried out under reduced pressure; in addition, the ionic liquid could be reused without loss of effectiveness. These features contribute to the significant advantages of this novel aryl C-glycosylation reaction.",
keywords = "Aryl C-glycosylation, Carbohydrate, Ionic liquid, Protic acid",
author = "Chigusa Yamada and Kaname Sasaki and Shuichi Matsumura and Kazunobu Toshima",
note = "Funding Information: This research was supported in part by a Grant-in-Aid for the 21st Century COE Program {\textquoteleft}KEIO Life Conjugated Chemistry{\textquoteright}, for Scientific Research on Priority Areas 18032068, and for JSPS Fellows 18·6013 from the Ministry of Education, Culture, Sports, Science, and Technology, Japan.",
year = "2007",
month = jun,
day = "11",
doi = "10.1016/j.tetlet.2007.04.077",
language = "English",
volume = "48",
pages = "4223--4227",
journal = "Tetrahedron Letters",
issn = "0040-4039",
publisher = "Elsevier Limited",
number = "24",
}