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A 1,10-hofmann elimination. Synthesis of a [6.6]paracyclopane tetraene

dc.contributor.authorGlatzhofer, Daniel T.en_US
dc.contributor.authorLongone, Daniel T.en_US
dc.date.accessioned2006-04-07T18:51:23Z
dc.date.available2006-04-07T18:51:23Z
dc.date.issued1983en_US
dc.identifier.citationGlatzhofer, Daniel T., Longone,, Daniel T. (1983)."A 1,10-hofmann elimination. Synthesis of a [6.6]paracyclopane tetraene." Tetrahedron Letters 24(41): 4413-4416. <http://hdl.handle.net/2027.42/25458>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6THS-42R1V7G-S5/2/b3d5fcf49a5fc8d58b06bef7f42324f2en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/25458
dc.description.abstractThe synthesis of (, , , ) - [6.6]paracyclophane-1,5,13,17-tetraene the [10+10] cyclodimerization of 7,8-divinyl-p-quinodimethane is described.en_US
dc.format.extent210278 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleA 1,10-hofmann elimination. Synthesis of a [6.6]paracyclopane tetraeneen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, The University of Michigan, Ann Arbor, Michigan 48109 U.S.A.en_US
dc.contributor.affiliationumDepartment of Chemistry, The University of Michigan, Ann Arbor, Michigan 48109 U.S.A.en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/25458/1/0000908.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/S0040-4039(00)85911-0en_US
dc.identifier.sourceTetrahedron Lettersen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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