完整後設資料紀錄
DC 欄位語言
dc.contributor.authorChen, Jiun-Hanen_US
dc.contributor.authorRuei, Jyh-Herngen_US
dc.contributor.authorMong, Kwok-Kong Tonyen_US
dc.date.accessioned2014-12-08T15:35:26Z-
dc.date.available2014-12-08T15:35:26Z-
dc.date.issued2014-03-01en_US
dc.identifier.issn1434-193Xen_US
dc.identifier.urihttp://dx.doi.org/10.1002/ejoc.201400006en_US
dc.identifier.urihttp://hdl.handle.net/11536/23994-
dc.description.abstractThis paper describes the development of an iterative and -selective glycosylation method for 2-deoxyglycosyl and 2,6-dideoxythioglycoside donors based on the DMF modulation concept. We used NMR spectroscopy to probe the 2-deoxyglycosyl imidinium intermediate and elucidated the conditions to decrease the formation of glycal and thus to increase the reaction yields. Further elaboration of the glycosylation method opened the gate for an iterative one-pot synthesis of 2-deoxy- and 2,6-dideoxyglycoside-containing oligosaccharides.en_US
dc.language.isoen_USen_US
dc.titleIterative alpha-Glycosylation Strategy for 2-Deoxy- and 2,6-Dideoxysugars: Application to the One-Pot Synthesis of Deoxysugar-Containing Oligosaccharidesen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/ejoc.201400006en_US
dc.identifier.journalEUROPEAN JOURNAL OF ORGANIC CHEMISTRYen_US
dc.citation.volume2014en_US
dc.citation.issue9en_US
dc.citation.spage1827en_US
dc.citation.epage1831en_US
dc.contributor.department交大名義發表zh_TW
dc.contributor.departmentNational Chiao Tung Universityen_US
顯示於類別:期刊論文