dc.creator | Vulović, Bojan | |
dc.creator | Kolarski, Dusan | |
dc.creator | Bihelović, Filip | |
dc.creator | Matović, Radomir | |
dc.creator | Gruden, Maja | |
dc.creator | Saičić, Radomir N. | |
dc.date.accessioned | 2019-01-30T17:48:14Z | |
dc.date.available | 2019-01-30T17:48:14Z | |
dc.date.issued | 2016 | |
dc.identifier.issn | 1523-7060 | |
dc.identifier.uri | https://cer.ihtm.bg.ac.rs/handle/123456789/1847 | |
dc.description.abstract | 1,6-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.publisher | American Chemical Society (ACS) | |
dc.relation | info:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172027/RS// | |
dc.relation | info:eu-repo/grantAgreement/EC/FP7/256716/EU// | |
dc.relation | Serbian Academy of Sciences and Arts [F193] | |
dc.rights | restrictedAccess | |
dc.source | Organic Letters | |
dc.title | Gold(I)-Catalyzed Domino Cyclizations of Diynes for the Synthesis of Functionalized Cyclohexenone Derivatives. Total Synthesis of (-)-Gabosine H and (-)-6-epi-Gabosine H | en |
dc.type | article | |
dc.rights.license | ARR | |
dcterms.abstract | Вуловиц, Бојан; Саициц, Радомир Н; Матовић, Радомир; Коларски, Дусан; Бихеловиц, Филип; Груден, Маја; | |
dc.citation.volume | 18 | |
dc.citation.issue | 15 | |
dc.citation.spage | 3886 | |
dc.citation.epage | 3889 | |
dc.citation.other | 18(15): 3886-3889 | |
dc.citation.rank | aM21 | |
dc.identifier.pmid | 27456978 | |
dc.identifier.doi | 10.1021/acs.orglett.6b01898 | |
dc.identifier.scopus | 2-s2.0-84981188263 | |
dc.identifier.wos | 000381236300095 | |
dc.type.version | publishedVersion | |