2-Allylphenyl glycosides as glycosyl donors for sugar coupling
| dc.citation.epage | 197 | en_US |
| dc.citation.issue | en_US | |
| dc.citation.volume | 352 | en_US |
| dc.citation.woscount | 5 | |
| dc.contributor.author | Luo, Shun-Yuan | en_US |
| dc.contributor.author | Tripathi, Ashish | en_US |
| dc.contributor.author | Zulueta, Medel Manuel L. | en_US |
| dc.contributor.author | Hung, Shang-Cheng | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:22:38Z | |
| dc.date.available | 2014-12-08T15:22:38Z | |
| dc.date.issued | 2012-05-01 | en_US |
| dc.description.abstract | Glycosylations employing 2-allylphenyl glycoside, a new type of stable glycosyl donor, were optimized and explored with a variety of acceptors promoted by ICl/AgOTf. The utility of the protocol was further demonstrated with an efficient synthesis of the disaccharide fragment of bleomycins. (C) 2012 Elsevier Ltd. All rights reserved. | en_US |
| dc.identifier.issn | 0008-6215 | en_US |
| dc.identifier.journal | CARBOHYDRATE RESEARCH | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/16004 | |
| dc.identifier.wosnumber | WOS:000302778000025 | |
| dc.language.iso | en_US | en_US |
| dc.subject | 2-Allylphenyl glycoside | en_US |
| dc.subject | Bleomycin | en_US |
| dc.subject | Glycosylation | en_US |
| dc.subject | D-Mannose | en_US |
| dc.subject | Stereoselectivity | en_US |
| dc.title | 2-Allylphenyl glycosides as glycosyl donors for sugar coupling | en_US |
| dc.type | Article | en_US |