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dc.creatorMatović, R.
dc.creatorBihelović, Filip
dc.creatorGruden-Pavlović, Maja
dc.creatorSaičić, Radomir
dc.date.accessioned2018-11-22T00:29:19Z
dc.date.available2018-11-22T00:29:19Z
dc.date.issued2014
dc.identifier.issn1477-0520
dc.identifier.urihttp://cherry.chem.bg.ac.rs/handle/123456789/1860
dc.description.abstractThe total synthesis of desmethylabyssomicin C analogue 1 was accomplished using diastereotopos-selective ring closing metathesis and Nozaki-Hiyama-Kishi cyclization as the key steps. The synthetic analogue retained its antibacterial activity against methicillin-resistant S. aureus strains, whereas its cytotoxicity decreased for three orders of magnitude, as compared to atrop-abyssomicin C.en
dc.publisherRoyal Soc Chemistry, Cambridge
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172027/RS//
dc.relationSerbian Academy of Sciences and Arts [F193]
dc.rightsrestrictedAccess
dc.sourceOrganic and Biomolecular Chemistry
dc.titleTotal synthesis and biological evaluation of atrop-O-benzyl-desmethylabyssomicin Cen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractСаичић, Радомир; Бихеловић, Филип; Груден-Павловић, Маја; Матовиц, Р.;
dc.citation.volume12
dc.citation.issue39
dc.citation.spage7682
dc.citation.epage7685
dc.identifier.wos000342886000005
dc.identifier.doi10.1039/c4ob01436g
dc.citation.other12(39): 7682-7685
dc.citation.rankM21
dc.identifier.pmid25166901
dc.type.versionpublishedVersionen
dc.identifier.scopus2-s2.0-84907867681
dc.identifier.rcubKon_2743


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