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dc.contributor.authorRuei, Jyh-Herngen_US
dc.contributor.authorVenukumar, Pattetien_US
dc.contributor.authorIngle, Arun B.en_US
dc.contributor.authorMong, Kwok-Kong Tonyen_US
dc.date.accessioned2015-07-21T08:28:25Z-
dc.date.available2015-07-21T08:28:25Z-
dc.date.issued2015-01-01en_US
dc.identifier.issn1359-7345en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c4cc08465aen_US
dc.identifier.urihttp://hdl.handle.net/11536/124591-
dc.description.abstractWe reported a remote control glycosylation method using the picoloyl protecting group for 2-deoxy-beta-glycosidic bond formation. The method is applicable to various 2-deoxythioglycosyl donors and the utility is illustrated by the synthesis of a deoxytrisaccharide component of landomycins.en_US
dc.language.isoen_USen_US
dc.titleC6 picoloyl protection: a remote stereodirecting group for 2-deoxy-beta-glycoside formationen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c4cc08465aen_US
dc.identifier.journalCHEMICAL COMMUNICATIONSen_US
dc.citation.volume51en_US
dc.citation.issue25en_US
dc.citation.spage5394en_US
dc.citation.epage5397en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000351393600047en_US
dc.citation.woscount1en_US
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