Preparation of tricyclic nitrogen heterocycle via Intramolecular Diels-Alder reaction

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dc.authorid0000-0001-9133-875X
dc.contributor.authorDemircan, A
dc.contributor.authorParsons, PJ
dc.date.accessioned2019-08-01T13:38:39Z
dc.date.available2019-08-01T13:38:39Z
dc.date.issued2002
dc.departmentNiğde ÖHÜ
dc.description.abstractPreparation of rigid tricyclic nitrogen heterocycles under radicalic condition has been studied. Cyclisation is performed by Diels-Alder ring closure after radicalic hydrogenation. We did not observe any radicalic Cycloaddition / Fragmentation product 12. Tri-n-butyltin hydride (TBTH) and azobisisobutyronitrile were used in toluene or benzene to generate radicalic condition. Intramolecular, Diels-Alder (IMDA) reaction on substituted furan species gave tricyclic heterocycle.
dc.identifier.endpage536
dc.identifier.issn0793-0283
dc.identifier.issue6
dc.identifier.scopus2-s2.0-0036978793
dc.identifier.scopusqualityQ3
dc.identifier.startpage531
dc.identifier.urihttps://hdl.handle.net/11480/5739
dc.identifier.volume8
dc.identifier.wosWOS:000180495000002
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.institutionauthor[0-Belirlenecek]
dc.language.isoen
dc.publisherFREUND PUBLISHING HOUSE LTD
dc.relation.ispartofHETEROCYCLIC COMMUNICATIONS
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjecttri-n-butyltin hydride (TBTH)
dc.subjectazobisisobutyronitrile (AIBN)
dc.subjectintramolecular Diels-Alder reaction (IMDA)
dc.subjectcycloaddition
dc.titlePreparation of tricyclic nitrogen heterocycle via Intramolecular Diels-Alder reaction
dc.typeArticle

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