Preparation of heterotricyclic chlorides via intramolecular Diels-Alder reaction of furans

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dc.contributor.authorKaraarslan, Muhsin
dc.contributor.authorDemircan, Aydin
dc.date.accessioned2019-08-01T13:38:39Z
dc.date.available2019-08-01T13:38:39Z
dc.date.issued2007
dc.departmentNiğde ÖHÜ
dc.description.abstractA variety of key precursors to the intramolecular Diels-Alder (IMDA) reaction of furan diene have been prepared via facile alkylation. Subsequently, rigid heterotricyclic chlorides 5a-e possessing oxygen, nitrogen and sulfur have been synthesized by employing a thermal IMDA reactions. Use of bulky protecting group on nitrogen 5a-b, such as t-butoxy group, can be utilized to encourage cycloaddition reactions that otherwise does not proceed.
dc.identifier.endpage3006
dc.identifier.issn0970-7077
dc.identifier.issue4
dc.identifier.scopus2-s2.0-34547147864
dc.identifier.scopusqualityQ4
dc.identifier.startpage2999
dc.identifier.urihttps://hdl.handle.net/11480/5370
dc.identifier.volume19
dc.identifier.wosWOS:000251463400079
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.institutionauthor[0-Belirlenecek]
dc.language.isoen
dc.publisherASIAN JOURNAL OF CHEMISTRY
dc.relation.ispartofASIAN JOURNAL OF CHEMISTRY
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectintramolecular Diels-Alder
dc.subjectcycloaddition
dc.subjectfurfurylchloroalkenes
dc.titlePreparation of heterotricyclic chlorides via intramolecular Diels-Alder reaction of furans
dc.typeArticle

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