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Synthesis of indolidines by the 1,3-dipolar cycloaddition of azides with methylenecyclopropanes followed by cyclopropyumine rearrangement

dc.contributor.authorHeidt, Philip C.en_US
dc.contributor.authorBergmeier, Stephen C.en_US
dc.contributor.authorPearson, William H.en_US
dc.date.accessioned2006-04-10T13:59:46Z
dc.date.available2006-04-10T13:59:46Z
dc.date.issued1990en_US
dc.identifier.citationHeidt.++, Philip C., Bergmeier+, Stephen C., Pearson++,, WilliAm H. (1990)."Synthesis of indolidines by the 1,3-dipolar cycloaddition of azides with methylenecyclopropanes followed by cyclopropyumine rearrangement." Tetrahedron Letters 31(38): 5441-5444. <http://hdl.handle.net/2027.42/28967>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6THS-42H22BG-8R/2/02bb7dc14462b40d2aa0af9e6305c55aen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/28967
dc.description.abstractCyclic imines 6a and 6b were obtained by the intramolecular 1,3-dipolar cycloaddition of azides with methylenecyclopropanes. Acid catalyzed rearrangement produced bicyclic (-)-enamines 7, which upon reduction provided indoilizidenes 8. A similar strategy was used for the synthesis of (-)-8a-epi-desacctoxyslaframine 16.en_US
dc.format.extent329469 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleSynthesis of indolidines by the 1,3-dipolar cycloaddition of azides with methylenecyclopropanes followed by cyclopropyumine rearrangementen_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‡ and Department of Medicinal Chemistry† The University of Michigan, Ann arbor, MI 48109 U.S.A.en_US
dc.contributor.affiliationumDepartment of Chemistry‡ and Department of Medicinal Chemistry† The University of Michigan, Ann arbor, MI 48109 U.S.A.en_US
dc.contributor.affiliationumDepartment of Chemistry‡ and Department of Medicinal Chemistry† The University of Michigan, Ann arbor, MI 48109 U.S.A.en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/28967/1/0000804.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/S0040-4039(00)97867-5en_US
dc.identifier.sourceTetrahedron Lettersen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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