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Chemical Glycosylation with p-Methoxyphenyl (PMP) Glycosides via Oxidative Activation

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dc.contributor.authorKim, Hyun Su-
dc.contributor.authorJang, Eunbin-
dc.contributor.authorKim, Hoe In-
dc.contributor.authorBabu, Madala Hari-
dc.contributor.authorLee, Jae-Young-
dc.contributor.authorKim, Sang Kyum-
dc.contributor.authorSim, Jaehoon-
dc.date.accessioned2024-04-26T00:23:43Z-
dc.date.available2024-04-26T00:23:43Z-
dc.date.created2024-04-25-
dc.date.issued2023-05-
dc.identifier.citationORGANIC LETTERS, Vol.25 No.19, pp.3471-3475-
dc.identifier.issn1523-7060-
dc.identifier.urihttps://hdl.handle.net/10371/199458-
dc.description.abstractA novel persulfate-mediated oxidative glycosylation system using p-methoxyphenyl (PMP) glycosides as bench-stable glycosyl donors is developed. This study shows that both K2S2O8 as an oxidant and Hf(OTf)4 as a Lewis acid catalyst play important roles in the oxidative activation of the PMP group into a potential leaving group. This convenient glycosylation protocol proceeds under mild conditions and delivers a wide range of biologically and synthetically valuable glycoconjugates, including glycosyl fluorides.-
dc.language영어-
dc.publisherAMER CHEMICAL SOC-
dc.titleChemical Glycosylation with p-Methoxyphenyl (PMP) Glycosides via Oxidative Activation-
dc.typeArticle-
dc.identifier.doi10.1021/acs.orglett.3c01050-
dc.citation.journaltitleORGANIC LETTERS-
dc.identifier.wosid000984662300001-
dc.identifier.scopusid2-s2.0-85159609225-
dc.citation.endpage3475-
dc.citation.number19-
dc.citation.startpage3471-
dc.citation.volume25-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorLee, Jae-Young-
dc.type.docTypeArticle-
dc.description.journalClass1-
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  • College of Pharmacy
  • Department of Pharmacy
Research Area Biomaterial-based nano-platforms for cancer drug delivery and imaging, Formulation design and development, Functional protein expression and evaluation for drug delivery and therapy applications

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