A straightforward alpha-selective aromatic glycosylation and its application for stereospecific synthesis of 4-methylumbelliferyl alpha-T-antigen

doi:10.1016/j.carres.2008.12.013

完整後設資料紀錄

DC 欄位	值	語言
dc.contributor.author	Chang, Shih-Sheng	en_US
dc.contributor.author	Lin, Chun-Cheng	en_US
dc.contributor.author	Li, Yaw-Kuen	en_US
dc.contributor.author	Mong, Kwok-Kong Tony	en_US
dc.date.accessioned	2014-12-08T15:09:47Z	-
dc.date.available	2014-12-08T15:09:47Z	-
dc.date.issued	2009-03-10	en_US
dc.identifier.issn	0008-6215	en_US
dc.identifier.uri	http://dx.doi.org/10.1016/j.carres.2008.12.013	en_US
dc.identifier.uri	http://hdl.handle.net/11536/7494	-
dc.description.abstract	A practical and efficient alpha-selective aromatic glycosylation with simple per-O-acetyl glycopyranosyl trichloroacetimidates is reported. The method is particularly effective for L-fucosyl and 2-azido-2-deoxy-D-galatosaminyl imidates, with which exclusive alpha-selectivity was achieved. The synthetic utility of this method was demonstrated in the stereoselective synthesis of 4-methylumbelliferyl alpha-T-antigen. (C) 2008 Elsevier Ltd. All rights reserved.	en_US
dc.language.iso	en_US	en_US
dc.subject	Stereoselective	en_US
dc.subject	Aromatic	en_US
dc.subject	Glycosylation	en_US
dc.subject	Imidate	en_US
dc.subject	alpha-T-Antigen	en_US
dc.title	A straightforward alpha-selective aromatic glycosylation and its application for stereospecific synthesis of 4-methylumbelliferyl alpha-T-antigen	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1016/j.carres.2008.12.013	en_US
dc.identifier.journal	CARBOHYDRATE RESEARCH	en_US
dc.citation.volume	344	en_US
dc.citation.issue	4	en_US
dc.citation.spage	432	en_US
dc.citation.epage	438	en_US
dc.contributor.department	應用化學系	zh_TW
dc.contributor.department	Department of Applied Chemistry	en_US
dc.identifier.wosnumber	WOS:000264615900003	-
dc.citation.woscount	6	-
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