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Cycloaddition reactions of 1,4-dihydronaphthalene-1,4-epoxide with cyclohexadiene and 7-(methoxycarbonyl)cycloheptatriene: Selectivity in additions

dc.contributor.authorMenzek, A
dc.contributor.authorAltundas, A
dc.contributor.authorCoruh, U
dc.contributor.authorAkbulut, N
dc.contributor.authorLopez, EMV
dc.contributor.authorHokelek, T
dc.contributor.authorErdonmez, A
dc.date.accessioned2020-06-21T15:43:18Z
dc.date.available2020-06-21T15:43:18Z
dc.date.issued2004
dc.identifier.issn1434-193X
dc.identifier.issn1099-0690
dc.identifier.urihttps://doi.org/10.1002/ejoc.200300569
dc.identifier.urihttps://hdl.handle.net/20.500.12712/21573
dc.descriptionVazquez-Lopez, Ezequiel M./0000-0002-6012-0931; Hokelek, Tuncer/0000-0002-8602-4382en_US
dc.descriptionWOS: 000220048400026en_US
dc.description.abstractCycloaddition reactions of naphthalene-1,4-epoxide (1) with both 7-(methoxycarbonyl)cycloheptatriene (2) and cyclohexadiene (4) give adducts of type 3 and 5 exclusively. Selectivity was observed for the cycloaddition and bromination reactions, but neighboring group participation also occurrs in the latter. The formation of the products is discussed. (C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.en_US
dc.language.isoengen_US
dc.publisherWiley-V C H Verlag Gmbhen_US
dc.relation.isversionof10.1002/ejoc.200300569en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectalcoholsen_US
dc.subjectbrominationen_US
dc.subjectcycloadditionen_US
dc.subjecthalogenationen_US
dc.titleCycloaddition reactions of 1,4-dihydronaphthalene-1,4-epoxide with cyclohexadiene and 7-(methoxycarbonyl)cycloheptatriene: Selectivity in additionsen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume2004en_US
dc.identifier.issue5en_US
dc.identifier.startpage1143en_US
dc.identifier.endpage1148en_US
dc.relation.journalEuropean Journal of Organic Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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