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Reactions of vinyl selenoxides and ketenes via 3,3-sigmatropic rearrangement

dc.contributor.authorMarino, J. P.en_US
dc.contributor.authorKim, Min Wooen_US
dc.date.accessioned2006-04-07T20:05:05Z
dc.date.available2006-04-07T20:05:05Z
dc.date.issued1987en_US
dc.identifier.citationMarino,, J. P., Kim, Min Woo (1987)."Reactions of vinyl selenoxides and ketenes via 3,3-sigmatropic rearrangement." Tetrahedron Letters 28(42): 4925-4928. <http://hdl.handle.net/2027.42/27013>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6THS-42HXRSX-1TJ/2/5f38d9d32275c270df58ff9f7e5c2456en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/27013
dc.description.abstractThe reactions of several vinyl selenoxides with chlorocyano-ketene proceed a 3,3-sigmatropic rearrangement of an enolate oxyselenonium species to yield seleno-substituted [gamma]-butyrolactones.en_US
dc.format.extent191359 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleReactions of vinyl selenoxides and ketenes via 3,3-sigmatropic 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, 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/2027.42/27013/1/0000580.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/S0040-4039(00)96660-7en_US
dc.identifier.sourceTetrahedron Lettersen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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