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dc.contributor.authorLuo, Shun-Yuanen_US
dc.contributor.authorTripathi, Ashishen_US
dc.contributor.authorZulueta, Medel Manuel L.en_US
dc.contributor.authorHung, Shang-Chengen_US
dc.date.accessioned2014-12-08T15:22:38Z-
dc.date.available2014-12-08T15:22:38Z-
dc.date.issued2012-05-01en_US
dc.identifier.issn0008-6215en_US
dc.identifier.urihttp://hdl.handle.net/11536/16004-
dc.description.abstractGlycosylations 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.language.isoen_USen_US
dc.subject2-Allylphenyl glycosideen_US
dc.subjectBleomycinen_US
dc.subjectGlycosylationen_US
dc.subjectD-Mannoseen_US
dc.subjectStereoselectivityen_US
dc.title2-Allylphenyl glycosides as glycosyl donors for sugar couplingen_US
dc.typeArticleen_US
dc.identifier.journalCARBOHYDRATE RESEARCHen_US
dc.citation.volume352en_US
dc.citation.issueen_US
dc.citation.epage197en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000302778000025-
dc.citation.woscount5-
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