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Article: A Stereoselective Ring-Closing Glycosylation via Nonglycosylating Pathway

TitleA Stereoselective Ring-Closing Glycosylation via Nonglycosylating Pathway
Authors
Liu, HLi, X
Issue Date2014
PublisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/joc
Citation
The Journal of Organic Chemistry, 2014, v. 79 n. 12, p. 5834-5841 How to Cite?
DOI: http://dx.doi.org/10.1021/jo5006763
AbstractTwo glycosyl partners were first coupled with as ester linkage, which upon reductive acetylation produced an α-acetoxy ether group. The subsequent activation with TfOH triggered the ring-closing process and provided the corresponding glycosidic bond in high β-selectivity without relying on neighboring group participation.
Persistent Identifierhttp://hdl.handle.net/10722/202611
ISSN
0022-3263
2023 Impact Factor: 3.3
2023 SCImago Journal Rankings: 0.724
ISI Accession Number ID
WOS:000337871100048
Errata
http://dx.doi.org/10.1021/jo501874d
eid_2-s2.0-84924308113

 

DC FieldValueLanguage
dc.contributor.authorLiu, H-
dc.contributor.authorLi, X-
dc.date.accessioned2014-09-19T08:42:31Z-
dc.date.available2014-09-19T08:42:31Z-
dc.date.issued2014-
dc.identifier.citationThe Journal of Organic Chemistry, 2014, v. 79 n. 12, p. 5834-5841-
dc.identifier.issn0022-3263-
dc.identifier.urihttp://hdl.handle.net/10722/202611-
dc.description.abstractTwo glycosyl partners were first coupled with as ester linkage, which upon reductive acetylation produced an α-acetoxy ether group. The subsequent activation with TfOH triggered the ring-closing process and provided the corresponding glycosidic bond in high β-selectivity without relying on neighboring group participation.-
dc.languageeng-
dc.publisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/joc-
dc.relation.ispartofThe Journal of Organic Chemistry-
dc.titleA Stereoselective Ring-Closing Glycosylation via Nonglycosylating Pathway-
dc.typeArticle-
dc.identifier.emailLiu, H: liuhan@hku.hk-
dc.identifier.emailLi, X: xuechenl@hku.hk-
dc.identifier.authorityLiu, H=rp02748-
dc.identifier.authorityLi, X=rp00742-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/jo5006763-
dc.identifier.pmid24877607-
dc.identifier.scopuseid_2-s2.0-84903194662-
dc.identifier.hkuros239976-
dc.identifier.volume79-
dc.identifier.issue12-
dc.identifier.spage5834-
dc.identifier.epage5841-
dc.identifier.isiWOS:000337871100048-
dc.publisher.placeUnited States-
dc.relation.erratumdoi:10.1021/jo501874d-
dc.relation.erratumeid:eid_2-s2.0-84924308113-
dc.identifier.issnl0022-3263-

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