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Cycloaddition of vinyl aziridines with unsaturated substrates. A novel rearrangement of an unsaturated nitro compound.
dc.contributor.authorHassner, Alfreden_US
dc.contributor.authorD'Costa, Rosarioen_US
dc.contributor.authorMcPhail, Andrew T.en_US
dc.contributor.authorButler, William M.en_US
dc.date.accessioned2006-04-07T18:13:46Z
dc.date.available2006-04-07T18:13:46Z
dc.date.issued1981en_US
dc.identifier.citationHassner,, Alfred, D'Costa, Rosario, McPhail, Andrew T., Butler, William (1981)."Cycloaddition of vinyl aziridines with unsaturated substrates. A novel rearrangement of an unsaturated nitro compound.." Tetrahedron Letters 22(38): 3691-3694. <http://hdl.handle.net/2027.42/24586>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6THS-42HXSDY-14X/2/4b21bfe90d4c64ca7692bfa50620c22ben_US
dc.identifier.urihttps://hdl.handle.net/2027.42/24586
dc.description.abstractVinylaziridine undergoes reaction with electrophilic acetylenes and olefins to produce 7-membered azepine derivatives. With [beta]-nitro-styrene however, a novel rearrangement occurs, presumably via an ene reaction to form , the structure of which is definitively shown by x-ray diffraction.en_US
dc.format.extent207807 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleCycloaddition of vinyl aziridines with unsaturated substrates. A novel rearrangement of an unsaturated nitro compound.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, The University of Michigan, Ann Arbor, Michigan 48104 USAen_US
dc.contributor.affiliationotherDepartment of Chemistry, State University of New York at Binghamton, N.Y. 13901 USAen_US
dc.contributor.affiliationotherDepartment of Chemistry, State University of New York at Binghamton, N.Y. 13901 USAen_US
dc.contributor.affiliationotherDepartment of Chemistry, Duke University, Durham, N.C. 27706 USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/24586/1/0000869.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/S0040-4039(01)81995-Xen_US
dc.identifier.sourceTetrahedron Lettersen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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