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Intramolecular azide-diene cycloadditions. An approach to fused bicyclic 3-pyrrolines based on a one-pot nitrene-diene cycloaddition equivalent.

dc.contributor.authorPearson, William H.en_US
dc.contributor.authorCelebuski, Joseph E.en_US
dc.contributor.authorPoon, Yam-Fooen_US
dc.contributor.authorDixon, Brian R.en_US
dc.contributor.authorGlans, Jeffrey H.en_US
dc.date.accessioned2006-04-07T19:41:34Z
dc.date.available2006-04-07T19:41:34Z
dc.date.issued1986en_US
dc.identifier.citationPearson,, William H., Celebuski, Joseph E., Poon, Yam-Foo, Dixon, Brian R., Glans, Jeffrey H. (1986)."Intramolecular azide-diene cycloadditions. An approach to fused bicyclic 3-pyrrolines based on a one-pot nitrene-diene cycloaddition equivalent.." Tetrahedron Letters 27(52): 6301-6304. <http://hdl.handle.net/2027.42/26464>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6THS-42R1W41-113/2/b954d30fe3580276c161f79d684cbc2cen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/26464
dc.description.abstractCyclization of heterosubstituted [omega]-azidodienes 11 provides fused bicyclic 3-pyrrolines 12 in one operation. These pyrrolines are potentially useful intermediates for natural products synthesis, as illustrated by further functionalization.en_US
dc.format.extent194999 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleIntramolecular azide-diene cycloadditions. An approach to fused bicyclic 3-pyrrolines based on a one-pot nitrene-diene cycloaddition equivalent.en_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, University of Michigan, Ann Arbor, MI 48109 USAen_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109 USAen_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109 USAen_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109 USAen_US
dc.contributor.affiliationumDepartment of Chemistry, University of Michigan, Ann Arbor, MI 48109 USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/26464/1/0000552.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/S0040-4039(00)87792-8en_US
dc.identifier.sourceTetrahedron Lettersen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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