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Article: Synthesis of protected sugar-amino acid hybrid molecules as platform for further derivatization

TitleSynthesis of protected sugar-amino acid hybrid molecules as platform for further derivatization
Authors
KeywordsHybrid molecule
Sugar
Amino acid
Depsipeptide
Issue Date2012
PublisherPergamon. The Journal's web site is located at http://www.elsevier.com/locate/tetlet
Citation
Tetrahedron Letters, 2012, v. 53 n. 51, p. 6957-6960 How to Cite?
AbstractThe sugar-amino acid hybrid molecules with appropriate protecting groups were synthesized from sugar-derived lactones and ester of amino acids in five high yielding steps. The C-5 of the resultant hybrid molecule, upon selective deprotection, can be further derivatized to afford the linear depsipeptide.
Persistent Identifierhttp://hdl.handle.net/10722/185677
ISSN
2021 Impact Factor: 2.032
2020 SCImago Journal Rankings: 0.541
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLiu, H-
dc.contributor.authorLi, X-
dc.date.accessioned2013-08-20T11:37:21Z-
dc.date.available2013-08-20T11:37:21Z-
dc.date.issued2012-
dc.identifier.citationTetrahedron Letters, 2012, v. 53 n. 51, p. 6957-6960-
dc.identifier.issn0040-4039-
dc.identifier.urihttp://hdl.handle.net/10722/185677-
dc.description.abstractThe sugar-amino acid hybrid molecules with appropriate protecting groups were synthesized from sugar-derived lactones and ester of amino acids in five high yielding steps. The C-5 of the resultant hybrid molecule, upon selective deprotection, can be further derivatized to afford the linear depsipeptide.-
dc.languageeng-
dc.publisherPergamon. The Journal's web site is located at http://www.elsevier.com/locate/tetlet-
dc.relation.ispartofTetrahedron Letters-
dc.subjectHybrid molecule-
dc.subjectSugar-
dc.subjectAmino acid-
dc.subjectDepsipeptide-
dc.titleSynthesis of protected sugar-amino acid hybrid molecules as platform for further derivatization-
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.doi10.1016/j.tetlet.2012.10.042-
dc.identifier.scopuseid_2-s2.0-84869220410-
dc.identifier.hkuros219109-
dc.identifier.volume53-
dc.identifier.issue51-
dc.identifier.spage6957-
dc.identifier.epage6960-
dc.identifier.isiWOS:000312231400022-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl0040-4039-

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