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dc.contributor.authorVeerapen, Natacha
dc.contributor.authorBrigl, Manfred
dc.contributor.authorGarg, Salil
dc.contributor.authorCerundolo, Vincenzo
dc.contributor.authorCox, Liam R.
dc.contributor.authorBrenner, Michael Barry
dc.contributor.authorBesra, Gurdyal S.
dc.date.accessioned2010-09-30T17:26:04Z
dc.date.issued2009
dc.identifier.citationVeerapen, Natacha, Manfred Brigl, Salil Garg, Vincenzo Cerundolo, Liam R. Cox, Michael B. Brenner, and Gurdyal S. Besra. 2009. Synthesis and biological activity of α-galactosyl ceramide KRN7000 and galactosyl (α1→2) galactosyl ceramide. Bioorganic & Medicinal Chemistry Letters 19(15): 4288-4291.en_US
dc.identifier.issn0960-894Xen_US
dc.identifier.urihttp://nrs.harvard.edu/urn-3:HUL.InstRepos:4454679
dc.description.abstractWe herein report a faster and less cumbersome synthesis of the biologically attractive, α-galactosyl ceramide (α-GalCer), known as KRN7000, and its analogues. More importantly, the use of a silicon tethered intramolecular glycosylation reaction gave easy access to the diglycosyl ceramide Gal(α1→2)GalCer, which has been shown to require uptake and processing to the biologically active α-GalCer derivative.en_US
dc.description.sponsorshipEngineering and Applied Sciencesen_US
dc.language.isoen_USen_US
dc.publisherElsevier Science Ltden_US
dc.relation.isversionofdoi:10.1016/j.bmcl.2009.05.095en_US
dc.relation.hasversionhttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC2722241/pdf/en_US
dash.licenseOAP
dc.titleSynthesis and Biological Activity of α-Galactosyl Ceramide KRN7000 and Galactosyl (α1→2) Galactosyl Ceramideen_US
dc.typeJournal Articleen_US
dc.description.versionAccepted Manuscripten_US
dc.relation.journalBioorganic & Medicinal Chemistry Lettersen_US
dash.depositing.authorBrenner, Michael Barry
dc.date.available2010-09-30T17:26:04Z
dc.identifier.doi10.1016/j.bmcl.2009.05.095*
dash.contributor.affiliatedBrigl, Manfred
dash.contributor.affiliatedGarg, Salil
dash.contributor.affiliatedBrenner, Michael


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