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Reductive Heck reactions of N-arylamino-substituted tricyclic imides

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dc.contributor.authorAtbakar, Muge
dc.contributor.authorTopbastekin, Onur
dc.contributor.authorOcal, Nuket
dc.date.accessioned2026-06-27T13:53:23Z
dc.date.issued2016
dc.description.abstractThe C-C coupling of (3aR,4S,7R,7aS)-rel-2-[(3-chloro-4-fluorophenyl)amino]-3a, 4,7,7a-tetrahydro-4,7-methano-1H-isoindole-1,3(2H)-dione (3) which was prepared as a new starting material and (3aR, 4S, 7R, 7aS)-rel-2-[(2,4-dinitrophenyl) amino]-3a, 4,7,7a-tetrahydro-4,7-methano-1H-isoindole-1,3(2H)-dione (6) with aryl-and heteroaryl iodides gave the aryl(hetaryl), N-arylamino tricyclic imides 4a-d and 7a-d under reductive Heck conditions.en
dc.description.sponsorshipYildiz Technical University Scientific Research Projects Coordination Department [2014-01-02-KAP03]
dc.description.urihttps://doi.org/10.2298/jsc160218062a
dc.identifier.doi10.2298/jsc160218062a
dc.identifier.endpage1125
dc.identifier.issn0352-5139
dc.identifier.issue10
dc.identifier.startpage1121
dc.identifier.urihttps://hdl.handle.net/20.500.14981/55332
dc.identifier.volume81
dc.identifier.wos000388028400002
dc.language.isoeng
dc.publisherSERBIAN CHEMICAL SOC
dc.relation.ispartofJOURNAL OF THE SERBIAN CHEMICAL SOCIETY
dc.rightsopenAccess
dc.subjecthydroarylation reactions
dc.subjectcyclic hydrazines
dc.subjectimides
dc.subjectC-C coupling with Pd(OAc)(2)
dc.subjectPALLADIUM-CATALYZED REACTIONS
dc.subjectUNSATURATED DICARBOXIMIDES
dc.subjectCYCLIC IMIDES
dc.subjectDERIVATIVES
dc.subjectHYDROARYLATION
dc.subjectEPIBATIDINE
dc.subjectANTICANCER
dc.subjectHYDRAZINES
dc.subjectChemistry
dc.titleReductive Heck reactions of N-arylamino-substituted tricyclic imides
dc.typeArticle
dspace.entity.typePublication
local.import.sourceWOS

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