Приказ основних података о документу

dc.creatorMilićević, Selena
dc.creatorMatović, Radomir
dc.creatorSaičić, Radomir N.
dc.date.accessioned2019-04-28T15:58:11Z
dc.date.available2019-04-28T15:58:11Z
dc.date.issued2004
dc.identifier.issn0040-4039
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/2762
dc.description.abstractOptically pure (-)-cytoxazone was synthesized, starting from methyl p-methoxycinnamate, in six steps and in 31%, overall yield. The required anti-aminoalcohol configuration was established by combining Sharpless asymmetric aminohydroxylation with the configurational inversion of the intermediate amidoalcohol via ail oxazoline. The synthesis of (+)-epi-cytoxazone is also described. (C) 2003 Elsevier Ltd. All rights reserved.en
dc.publisherOxford : Pergamon-Elsevier Science Ltd
dc.rightsrestrictedAccess
dc.sourceTetrahedron Letters
dc.subjectcytoxazoneen
dc.subjectasymmetric synthesisen
dc.subjectnatural productsen
dc.subjectimmunosuppressive compoundsen
dc.subjectamino alcoholsen
dc.titleStereoselective synthesis of (-)-cytoxazone and (+)-epi-cytoxazoneen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractСаичић, Радомир Н.; Матовић, Радомир; Милићевић, Селена;
dc.rights.holderElsevier
dc.citation.volume45
dc.citation.issue5
dc.citation.spage955
dc.citation.epage957
dc.citation.other45(5): 955-957
dc.citation.rankM21
dc.identifier.doi10.1016/j.tetlet.2003.11.096
dc.identifier.scopus2-s2.0-0346392218
dc.identifier.wos000188380400015
dc.type.versionpublishedVersionen


Документи

Thumbnail

Овај документ се појављује у следећим колекцијама

Приказ основних података о документу