Please use this identifier to cite or link to this item: http://earsiv.odu.edu.tr:8080/xmlui/handle/11489/3150
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dc.contributor.authorKelebekli, Latif-
dc.date.accessioned2022-09-05T10:14:13Z-
dc.date.available2022-09-05T10:14:13Z-
dc.date.issued2013-
dc.identifier.urihttp://doi.org/10.1080/00397911.2012.754472-
dc.identifier.urihttp://earsiv.odu.edu.tr:8080/xmlui/handle/11489/3150-
dc.description.abstractStereoselective synthesis of tricyclo[6.2.2.0(2,7)]dodecane-3,6,9,10-tetrol was developed starting from p-benzoquinone. The endo selective Diels-Alder cycloaddition of p-benzoquinone and 1,3-cyclohexadiene afforded the corresponding bicyclic diketone. The synthesis of the title compound was based on the cycloadduct by selective reduction with NaBH4, acetylation with AcCl, and hydroxylation with OsO4-NMO. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications (R) for the following free supplemental resource: Full experimental and spectral details.]en_US
dc.language.isoengen_US
dc.publisherTAYLOR & FRANCIS INC530 WALNUT STREET, STE 850, PHILADELPHIA, PA 19106en_US
dc.relation.isversionof10.1080/00397911.2012.754472en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectStereoselective synthesis of tricyclo[6.2.2.0(2,7)]dodecane-3,6,9,10-tetrol was developed starting from p-benzoquinone. The endo selective Diels-Alder cycloaddition of p-benzoquinone and 1,3-cyclohexadiene afforded the corresponding bicyclic diketone. The synthesis of the title compound was based on the cycloadduct by selective reduction with NaBH4, acetylation with AcCl, and hydroxylation with OsO4-NMO. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications (R) for the following free supplemental resource: Full experimental and spectral details.]en_US
dc.titleStereoselective Synthesis of Tricyclo[6.2.2.0(2,7)]dodecane-3,6,9,10-tetrol via Selective Reduction of ,-Unsaturated 1,4-DIKetoneen_US
dc.typearticleen_US
dc.relation.journalSYNTHETIC COMMUNICATIONSen_US
dc.contributor.departmentOrdu Üniversitesien_US
dc.contributor.authorID0000-0002-6242-2589en_US
dc.identifier.volume43en_US
dc.identifier.issue22en_US
dc.identifier.startpage2998en_US
dc.identifier.endpage3009en_US
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