New tri- and tetra-substituted pyrroles via quinazolinium N1-ylides

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dc.contributor.authorCaira, Mino R
dc.contributor.authorGeorgescu, Emilian
dc.contributor.authorBarbu, Loredana
dc.contributor.authorGeorgescu, Florentina
dc.contributor.authorDumitraşcu, Florea
dc.date.accessioned2021-10-08T11:00:57Z
dc.date.available2021-10-08T11:00:57Z
dc.date.issued2011
dc.description.abstractNew tri-and tetra-substituted N-arylpyrroles were synthesized by one-pot reaction of 3,7-disubstituted quinazolinonium bromides with substituted alkynes having at least one electron-withdrawing substituent in 1,2-epoxybutane acting both as solvent and hydrogen bromide scavenger. Structural characterization of the new compounds was based on IR and NMR spectroscopy as well as on single crystal X-ray analysis.
dc.identifier.apacitationCaira, M. R., Georgescu, E., Barbu, L., Georgescu, F., & Dumitraşcu, F. (2011). New tri- and tetra-substituted pyrroles via quinazolinium N1-ylides. <i>ARKIVOC - Online Journal of Organic Chemistry</i>, 2011(10), 44 - 177. http://hdl.handle.net/11427/35053en_ZA
dc.identifier.chicagocitationCaira, Mino R, Emilian Georgescu, Loredana Barbu, Florentina Georgescu, and Florea Dumitraşcu "New tri- and tetra-substituted pyrroles via quinazolinium N1-ylides." <i>ARKIVOC - Online Journal of Organic Chemistry</i> 2011, 10. (2011): 44 - 177. http://hdl.handle.net/11427/35053en_ZA
dc.identifier.citationCaira, M.R., Georgescu, E., Barbu, L., Georgescu, F. & Dumitraşcu, F. 2011. New tri- and tetra-substituted pyrroles via quinazolinium N1-ylides. <i>ARKIVOC - Online Journal of Organic Chemistry.</i> 2011(10):44 - 177. http://hdl.handle.net/11427/35053en_ZA
dc.identifier.issn1424-6368
dc.identifier.issn1424-6376
dc.identifier.issn1551-7004
dc.identifier.issn1551-7012
dc.identifier.ris TY - Journal Article AU - Caira, Mino R AU - Georgescu, Emilian AU - Barbu, Loredana AU - Georgescu, Florentina AU - Dumitraşcu, Florea AB - New tri-and tetra-substituted N-arylpyrroles were synthesized by one-pot reaction of 3,7-disubstituted quinazolinonium bromides with substituted alkynes having at least one electron-withdrawing substituent in 1,2-epoxybutane acting both as solvent and hydrogen bromide scavenger. Structural characterization of the new compounds was based on IR and NMR spectroscopy as well as on single crystal X-ray analysis. DA - 2011 DB - OpenUCT DP - University of Cape Town IS - 10 J1 - ARKIVOC - Online Journal of Organic Chemistry LK - https://open.uct.ac.za PY - 2011 SM - 1424-6368 SM - 1424-6376 SM - 1551-7004 SM - 1551-7012 T1 - New tri- and tetra-substituted pyrroles via quinazolinium N1-ylides TI - New tri- and tetra-substituted pyrroles via quinazolinium N1-ylides UR - http://hdl.handle.net/11427/35053 ER - en_ZA
dc.identifier.urihttp://hdl.handle.net/11427/35053
dc.identifier.vancouvercitationCaira MR, Georgescu E, Barbu L, Georgescu F, Dumitraşcu F. New tri- and tetra-substituted pyrroles via quinazolinium N1-ylides. ARKIVOC - Online Journal of Organic Chemistry. 2011;2011(10):44 - 177. http://hdl.handle.net/11427/35053.en_ZA
dc.language.isoeng
dc.publisher.departmentDepartment of Chemistry
dc.publisher.facultyFaculty of Science
dc.sourceARKIVOC - Online Journal of Organic Chemistry
dc.source.journalissue10
dc.source.journalvolume2011
dc.source.pagination44 - 177
dc.source.urihttps://dx.doi.org/10.3998/ark.5550190.0012.a04
dc.subject.otherBurns
dc.subject.otherDisaster Planning
dc.subject.otherHumans
dc.subject.otherMass Casualty Incidents
dc.subject.otherNational Health Programs
dc.subject.otherPractice Guidelines as Topic
dc.subject.otherSocieties, Medical
dc.subject.otherSouth Africa
dc.titleNew tri- and tetra-substituted pyrroles via quinazolinium N1-ylides
dc.typeJournal Article
uct.type.publicationResearch
uct.type.resourceJournal Article
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