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Heck-type hydroarylations and 1,3-dipolar cycloaddition reactions of new tricyclic hydrazones

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dc.contributor.authorGul, Melek
dc.contributor.authorOcal, Nuket
dc.date.accessioned2026-06-27T12:51:37Z
dc.date.issued2010
dc.description.abstractThe C-C coupling of the new tricyclic hydrazones 3-7 with aryl and heteroaryl halides gave under reductive Heck conditions the tricyclic 1-(arylideneamino)pyrolidine-2,5-diones 8-11a, 9-11b, 10c, and 12. The [3+2] cycloadditions of 3-7 with p-chlorophenyl nitrile oxide (13) yielded the bridged isoxazoline derivatives 14-18 with potential biological activity.en
dc.description.sponsorshipYildiz Technical University [28-01-02-04]
dc.description.urihttps://doi.org/10.1139/v09-179
dc.identifier.doi10.1139/v09-179
dc.identifier.eissn1480-3291
dc.identifier.endpage330
dc.identifier.issn0008-4042
dc.identifier.issue4
dc.identifier.startpage323
dc.identifier.urihttps://hdl.handle.net/20.500.14981/47525
dc.identifier.volume88
dc.identifier.wos000277451300005
dc.language.isoeng
dc.publisherCANADIAN SCIENCE PUBLISHING
dc.relation.ispartofCANADIAN JOURNAL OF CHEMISTRY
dc.subjecttricyclic hydrazone
dc.subjectreductive Heck reactions
dc.subjectC-C coupling
dc.subjectnitrile oxides
dc.subjectisoxazolines
dc.subjectIRON CHELATORS
dc.subjectCHEMISTRY
dc.subjectEPIBATIDINE
dc.titleHeck-type hydroarylations and 1,3-dipolar cycloaddition reactions of new tricyclic hydrazones
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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