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Synthesis of [4.2]cyclophanes
dc.contributor.authorHammond, Philip S.en_US
dc.contributor.authorLongone, Daniel T.en_US
dc.date.accessioned2006-04-07T17:05:51Z
dc.date.available2006-04-07T17:05:51Z
dc.date.issued1978en_US
dc.identifier.citationHammond, Philip S., Longone,, Daniel T. (1978)."Synthesis of [4.2]cyclophanes." Tetrahedron Letters 19(5): 415-418. <http://hdl.handle.net/2027.42/22744>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6THS-42HG2BC-25V/2/fe598cd51b1a02e0389f354ec158df03en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/22744
dc.description.abstractVinyl -xylylene cross-dimerizes with other xylylene-type intermediates to yield cycloadducts of the [8+6] and [6+6] type. This reaction provides a simple entry to the [4.2]paracyclophane system as well as the analogous [4.2]cyclophanes containing furan and pyrrole moieties.en_US
dc.format.extent190525 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleSynthesis of [4.2]cyclophanesen_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 USAen_US
dc.contributor.affiliationumDepartment of Chemistry, The University of Michigan, Ann Arbor, Michigan 48109 USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/22744/1/0000299.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/S0040-4039(01)91442-Xen_US
dc.identifier.sourceTetrahedron Lettersen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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