Приказ основних података о документу

dc.creatorVulović, Bojan
dc.creatorKolarski, Dusan
dc.creatorBihelović, Filip
dc.creatorMatović, Radomir
dc.creatorGruden, Maja
dc.creatorSaičić, Radomir N.
dc.date.accessioned2019-01-30T17:48:14Z
dc.date.available2019-01-30T17:48:14Z
dc.date.issued2016
dc.identifier.issn1523-7060
dc.identifier.urihttps://cer.ihtm.bg.ac.rs/handle/123456789/1847
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.publisherAmerican Chemical Society (ACS)
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.abstractВуловиц, Бојан; Саициц, Радомир Н; Матовић, Радомир; Коларски, Дусан; Бихеловиц, Филип; Груден, Маја;
dc.citation.volume18
dc.citation.issue15
dc.citation.spage3886
dc.citation.epage3889
dc.citation.other18(15): 3886-3889
dc.citation.rankaM21
dc.identifier.pmid27456978
dc.identifier.doi10.1021/acs.orglett.6b01898
dc.identifier.scopus2-s2.0-84981188263
dc.identifier.wos000381236300095
dc.type.versionpublishedVersion


Документи

Thumbnail

Овај документ се појављује у следећим колекцијама

Приказ основних података о документу