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dc.contributor.authorGhosh, Bhaswatien_US
dc.contributor.authorLai, Yen-Hsunen_US
dc.contributor.authorShih, Yu-Yinen_US
dc.contributor.authorPradhan, Tapan Kumaren_US
dc.contributor.authorLin, Chun-Hungen_US
dc.contributor.authorMong, Kwok-Kong Tonyen_US
dc.date.accessioned2014-12-08T15:33:26Z-
dc.date.available2014-12-08T15:33:26Z-
dc.date.issued2013-12-01en_US
dc.identifier.issn1861-4728en_US
dc.identifier.urihttp://dx.doi.org/10.1002/asia.201300933en_US
dc.identifier.urihttp://hdl.handle.net/11536/23229-
dc.description.abstractThe total synthesis of a glycoglycerolipid isolate of Meiothermus taiwanensis and its truncated structural analogues is reported. Our synthesis employed DMF-modulated and low-concentration glycosylation reactions for the construction of - and -glycosidic bonds in the absence of participating protecting groups. Further simplification of the synthesis was achieved by employing a low-concentration one-pot glycosylation procedure. Preliminary immunological studies showed that one of the truncated structural analogues suppressed the cytokine production of THP-1 monocytes.en_US
dc.language.isoen_USen_US
dc.subjectglycosylationen_US
dc.subjectimmunologyen_US
dc.subjectlipidsen_US
dc.subjectnatural productsen_US
dc.subjecttotal synthesisen_US
dc.titleTotal Synthesis of a Glycoglycerolipid from Meiothermus taiwanensis through a One-Pot Glycosylation Reaction and Exploration of its Immunological Propertiesen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/asia.201300933en_US
dc.identifier.journalCHEMISTRY-AN ASIAN JOURNALen_US
dc.citation.volume8en_US
dc.citation.issue12en_US
dc.citation.spage3191en_US
dc.citation.epage3199en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000327256100044-
dc.citation.woscount1-
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