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Cycloaddition Reactions of Some Tricyclic Imides

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dc.contributor.authorKulu, Irem
dc.contributor.authorGul, Melek
dc.contributor.authorGunkara, Omer Tahir
dc.contributor.authorOcal, Nuket
dc.contributor.institutionauthorGÜNKARA, Ömer Tahir
dc.date.accessioned2026-06-27T13:29:21Z
dc.date.issued2013
dc.description.abstractOur research group has published numerous papers over the last three years on the reaction of nitrile oxides and azomethine ylide with unsaturated tricyclic N-substituted dicarboximides selected according to the importance of possible biological activities. These reactions cover full range of mechanistic pathways and timings of bond-forming processes to give five-membered ring closure by 1,3-dipolar cycloaddition.en
dc.description.sponsorshipScientific and Technological Research Council of Turkey (TUBITAK) [109T380]
dc.description.sponsorshipYildiz Technical University scientific research projects coordination department [2011-01-02-KAP03]
dc.description.urihttps://doi.org/10.2174/1570193x113106660017
dc.identifier.doi10.2174/1570193x113106660017
dc.identifier.eissn1875-6298
dc.identifier.endpage418
dc.identifier.issn1570-193X
dc.identifier.issue4
dc.identifier.startpage409
dc.identifier.urihttps://hdl.handle.net/20.500.14981/53144
dc.identifier.volume10
dc.identifier.wos000328088800012
dc.language.isoeng
dc.publisherBENTHAM SCIENCE PUBL LTD
dc.relation.ispartofMINI-REVIEWS IN ORGANIC CHEMISTRY
dc.subjectAzomethine ylide
dc.subjectbiological active molecules
dc.subject1,3-dipolar cycloaddition
dc.subjecthydrazones
dc.subjectisoxazolines
dc.subjectnitrile oxides
dc.subjecttricyclic imides
dc.subjectSUBSTITUTED CYCLIC IMIDES
dc.subjectHECK-TYPE HYDROARYLATIONS
dc.subject5-HT1A RECEPTOR LIGANDS
dc.subjectANTIMICROBIAL ACTIVITY
dc.subjectIRON CHELATORS
dc.subjectTANDOSPIRONE
dc.subjectEPIBOXIDINE
dc.subjectAFFINITY
dc.subjectANALOGS
dc.subjectChemistry
dc.titleCycloaddition Reactions of Some Tricyclic Imides
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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