Please use this identifier to cite or link to this item: http://hdl.handle.net/2440/68627
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dc.contributor.authorHale, K.en
dc.contributor.authorManaviazar, S.en
dc.contributor.authorGeorge, J.en
dc.contributor.authorWalters, M.en
dc.contributor.authorDalby, S.en
dc.date.issued2009en
dc.identifier.citationOrganic Letters, 2009; 11(3):733-736en
dc.identifier.issn1523-7060en
dc.identifier.issn1523-7052en
dc.identifier.urihttp://hdl.handle.net/2440/68627-
dc.description.abstractAsymmetric total syntheses of (+)-azinothricin and (+)-kettapeptin have been completed through a common new pathway that exploits a highly chemoselective coupling reaction between the fully elaborated cyclodepsipeptide 5 and the glycal activated esters 3 and 4 at the final stages of both respective syntheses.en
dc.description.statementofresponsibilityKarl J. Hale, Soraya Manaviazar, Jonathan H. George, Marcus A. Walters, and Stephen M. Dalbyen
dc.language.isoenen
dc.publisherAmer Chemical Socen
dc.rightsCopyright © 2009 American Chemical Societyen
dc.subjectEsters; Depsipeptides; Peptides; Molecular Structure; Stereoisomerismen
dc.titleTotal Synthesis of (+)-Azinothricin and (+)-Kettapeptinen
dc.typeJournal articleen
dc.identifier.rmid0020105895en
dc.identifier.doi10.1021/ol802817ten
dc.identifier.pubid30958-
pubs.library.collectionChemistry publicationsen
pubs.verification-statusVerifieden
pubs.publication-statusPublisheden
dc.identifier.orcidGeorge, J. [0000-0002-7330-2160]en
Appears in Collections:Chemistry publications

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