完整後設資料紀錄
DC 欄位語言
dc.contributor.authorHu, Jhe-Cyuanen_US
dc.contributor.authorFeng, Ai-Fen Wendyen_US
dc.contributor.authorChang, Bo-Yaoen_US
dc.contributor.authorLin, Chun-Hungen_US
dc.contributor.authorMong, Kwok-Kong Tonyen_US
dc.date.accessioned2018-08-21T05:54:15Z-
dc.date.available2018-08-21T05:54:15Z-
dc.date.issued2017-07-07en_US
dc.identifier.issn1477-0520en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c7ob00839ben_US
dc.identifier.urihttp://hdl.handle.net/11536/145720-
dc.description.abstractA flexible 1,2-cis alpha-selective glycosylation strategy for a wide range of glycosyl donors and acceptors has been developed, which is based on an in situ adduct transformation protocol. Based on this strategy, both NFM-derived and iodide covalent adducts can be accessed for glycosylation. Using low temperature NMR spectroscopy, the aforementioned glycosyl adducts were detected.en_US
dc.language.isoen_USen_US
dc.titleA flexible 1,2-cis alpha-glycosylation strategy based on in situ adduct transformationen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c7ob00839ben_US
dc.identifier.journalORGANIC & BIOMOLECULAR CHEMISTRYen_US
dc.citation.volume15en_US
dc.citation.spage5345en_US
dc.citation.epage5356en_US
dc.contributor.department交大名義發表zh_TW
dc.contributor.departmentNational Chiao Tung Universityen_US
dc.identifier.wosnumberWOS:000404358300017en_US
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