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Article: Thio-mediated synthesis of derivatized N-linked glycopeptides using isonitrile chemistry

TitleThio-mediated synthesis of derivatized N-linked glycopeptides using isonitrile chemistry
Authors
Wu, XYuan, YLi, XDanishefsky, SJ
Issue Date2009
PublisherPergamon. The Journal's web site is located at http://www.elsevier.com/locate/tetlet
Citation
Tetrahedron Letters, 2009, v. 50 n. 32, p. 4666-4669 How to Cite?
DOI: http://dx.doi.org/10.1016/j.tetlet.2009.06.005
AbstractThe reaction of oligosaccharide isonitriles with peptide thioacids in the presence of bulky thiophenol as activator to provide N-linked glycopeptides at room temperature is described. © 2009 Elsevier Ltd. All rights reserved.
Persistent Identifierhttp://hdl.handle.net/10722/168383
ISSN
0040-4039
2021 Impact Factor: 2.032
2020 SCImago Journal Rankings: 0.541
ISI Accession Number ID
WOS:000267901800025
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorWu, Xen_US
dc.contributor.authorYuan, Yen_US
dc.contributor.authorLi, Xen_US
dc.contributor.authorDanishefsky, SJen_US
dc.date.accessioned2012-10-08T03:18:15Z-
dc.date.available2012-10-08T03:18:15Z-
dc.date.issued2009en_US
dc.identifier.citationTetrahedron Letters, 2009, v. 50 n. 32, p. 4666-4669en_US
dc.identifier.issn0040-4039en_US
dc.identifier.urihttp://hdl.handle.net/10722/168383-
dc.description.abstractThe reaction of oligosaccharide isonitriles with peptide thioacids in the presence of bulky thiophenol as activator to provide N-linked glycopeptides at room temperature is described. © 2009 Elsevier Ltd. All rights reserved.en_US
dc.languageengen_US
dc.publisherPergamon. The Journal's web site is located at http://www.elsevier.com/locate/tetleten_US
dc.relation.ispartofTetrahedron Lettersen_US
dc.titleThio-mediated synthesis of derivatized N-linked glycopeptides using isonitrile chemistryen_US
dc.typeArticleen_US
dc.identifier.emailLi, X:xuechenl@hku.hken_US
dc.identifier.authorityLi, X=rp00742en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1016/j.tetlet.2009.06.005en_US
dc.identifier.scopuseid_2-s2.0-67449099147en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-67449099147&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume50en_US
dc.identifier.issue32en_US
dc.identifier.spage4666en_US
dc.identifier.epage4669en_US
dc.identifier.isiWOS:000267901800025-
dc.publisher.placeUnited Kingdomen_US
dc.identifier.scopusauthoridWu, X=7408235765en_US
dc.identifier.scopusauthoridYuan, Y=35180688100en_US
dc.identifier.scopusauthoridLi, X=24168958800en_US
dc.identifier.scopusauthoridDanishefsky, SJ=7202925243en_US
dc.identifier.issnl0040-4039-

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