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Imidazolone derivatives synthesis promoted by 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU)

dc.creatorPetković, Miloš
dc.creatorJovanović, Predrag
dc.creatorSimić, Milena
dc.creatorTasić, Gordana
dc.creatorSavić, Vladimir
dc.date.accessioned2023-12-26T13:08:13Z
dc.date.available2023-12-26T13:08:13Z
dc.date.issued2017
dc.identifier.isbn978-86-7132-067-2
dc.identifier.urihttps://farfar.pharmacy.bg.ac.rs/handle/123456789/5382
dc.description.abstractImidazoloni 2 pokazuju različita zanimljiva svojstva u biologiji, farmakologiji i fotohemiji.1,2 Razvijena je blaga i efikasna intramolekulska ciklizacija diamidnih jedinjenja 1, dobijenih Ugijevom reakcijom, koja dovodi do nastanka derivata imidazolona. Ovom transformacijom se dobijaju proizvodi u dobrim prinosima u kratkom reakcionom vremenusr
dc.description.abstractImidazolones 2 exhibit a variety of interesting properties in biology, pharmacology and photochemistry.1,2 Mild and efficient intramolecular cyclization of diamide compounds, obtained by the Ugi reaction, leading to imidazolone derivatives has been developed. The transformation affords the products in good yields in a short reaction time.sr
dc.language.isosrsr
dc.language.isoensr
dc.publisherSrpsko hemijsko društvo, Beogradsr
dc.relationinfo:eu-repo/grantAgreement/MESTD/Basic Research (BR or ON)/172009/RS//sr
dc.rightsopenAccesssr
dc.source54. Savetovanje Srpskog hemijskog društva. 5. Konferencija mladih hemičara Srbije. Kratki izvodi, Septembar 29 i 30, 2017, Beograd, Srbijasr
dc.titleSinteza derivata imidazolona promovisana pomoću 1,8-diazabiciklo[5.4.0]undec-7-ena (DBU)sr
dc.titleImidazolone derivatives synthesis promoted by 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU)sr
dc.typeconferenceObjectsr
dc.rights.licenseARRsr
dc.citation.spage88
dc.citation.epage88
dc.description.otherFifth Conference of Young Chemists of Serbia. September 29-30. 2017. Belgrade, Serbia
dc.identifier.fulltexthttp://farfar.pharmacy.bg.ac.rs/bitstream/id/15108/Sinteza_derivata_imidazolona_pub_2017.pdf
dc.identifier.rcubhttps://hdl.handle.net/21.15107/rcub_farfar_5382
dc.type.versionpublishedVersionsr


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