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dc.creatorTokic-Vujosevic, Z
dc.creatorPetrović, G
dc.creatorRakić, B
dc.creatorMatović, Radomir
dc.creatorSaičić, Radomir N.
dc.date.accessioned2019-04-29T07:36:55Z
dc.date.available2019-04-29T07:36:55Z
dc.date.issued2005
dc.identifier.issn0039-7911
dc.identifier.urihttp://cer.ihtm.bg.ac.rs/handle/123456789/2769
dc.description.abstractImmunomodulator (-)-cytoxazone and its epimer (+)-epi-cytoxazone were synthesized starting from (D)-(-)-4-hydroxyphenylglycine. Homologation of the amino acid was achieved via the corresponding aldehyde, by a cyanohydrin reaction. The racemization of highly sensible amido aldehyde was efficiently suppressed when the oxidation of the parent aminoalcohol was performed by a modified Dess-Martin procedure.en
dc.publisherTaylor & Francis
dc.rightsrestrictedAccess
dc.sourceSynthetic Communications
dc.subjectamino alcoholsen
dc.subjectcyanohydrinsen
dc.subjectcytoxazoneen
dc.subjectoxazolinesen
dc.titleSynthesis of (-)-cytoxazone and (+)-epi-cytoxazone: The chiral pool approachen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractСаичић, Радомир Н.; Матовић, Радомир; Токиц-Вујосевиц, З; Петровић, Г; Ракић, Б;
dc.rights.holderTaylor & Francis
dc.citation.volume35
dc.citation.issue3
dc.citation.spage435
dc.citation.epage447
dc.citation.other35(3): 435-447
dc.citation.rankM23
dc.identifier.doi10.1081/SCC-200048953
dc.identifier.scopus2-s2.0-14644411112
dc.identifier.wos000227372500012
dc.type.versionpublishedVersion


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