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dc.creatorVulović, Bojan
dc.creatorKolarski, Dušan
dc.creatorBihelović, Filip
dc.creatorMatović, Radomir
dc.creatorGruden-Pavlović, Maja
dc.creatorSaičić, Radomir
dc.date.accessioned2018-11-22T00:36:27Z
dc.date.available2018-11-22T00:36:27Z
dc.date.issued2016
dc.identifier.issn1523-7060
dc.identifier.urihttp://cherry.chem.bg.ac.rs/handle/123456789/2290
dc.description.abstract1,6-Diynes with a t-butylcarbonate group in the propargylic position undergo gold(I)-catalyzed dominocyclization which affords alpha-hydroxycyclohexenones. The described sequence can be applied on functionalized, highly oxygenated substrates, as examplified in the synthesis of (-)-gabosine H and its epimer.en
dc.publisherAmer Chemical Soc, Washington
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172027/RS//
dc.relationinfo:eu-repo/grantAgreement/EC/FP7/256716/EU//
dc.relationSerbian Academy of Sciences and Arts [F193]
dc.rightsrestrictedAccess
dc.sourceOrganic Letters
dc.titleGold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine Hen
dc.typearticle
dc.rights.licenseARR
dcterms.abstractВуловић, Бојан; Саичић, Радомир; Коларски, Дусан; Матовиц, Радомир; Груден-Павловић, Маја; Бихеловић, Филип;
dc.citation.volume18
dc.citation.issue15
dc.citation.spage3886
dc.citation.epage3889
dc.identifier.wos000381236300095
dc.identifier.doi10.1021/acs.orglett.6b01898
dc.citation.other18(15): 3886-3889
dc.citation.rankM21
dc.identifier.pmid27456978
dc.description.otherSupplementary material: [http://cherry.chem.bg.ac.rs/handle/123456789/3520]
dc.type.versionpublishedVersionen
dc.identifier.scopus2-s2.0-84981188263
dc.identifier.rcubKon_3106


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