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cis-2-Tri-n-butylstannylvinyl cuprates: a new synthon for the cis-1,2-ethene dianion
dc.contributor.authorMarino, J. P.en_US
dc.contributor.authorEmonds, Mark V. M.en_US
dc.contributor.authorStengel, Peter J.en_US
dc.contributor.authorOliveira, Alfredo R. M.en_US
dc.contributor.authorSimonelli, Fabioen_US
dc.contributor.authorFerreira, J. Tercio B.en_US
dc.date.accessioned2006-04-10T15:22:47Z
dc.date.available2006-04-10T15:22:47Z
dc.date.issued1992-01-01en_US
dc.identifier.citationMarino,, J. P., Emonds, Mark V. M., Stengel, Peter J., Oliveira, Alfredo R. M., Simonelli, Fabio, Ferreira, J. Tercio B. (1992/01/01)."cis-2-Tri-n-butylstannylvinyl cuprates: a new synthon for the cis-1,2-ethene dianion." Tetrahedron Letters 33(1): 49-52. <http://hdl.handle.net/2027.42/30275>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6THS-42HX4WM-C/2/f052735ab3f012777d71a8842d3de8efen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/30275
dc.description.abstractConjugate additions of lower order and higher order cyano cuprates containing the cis-2-tri-n-butylstannylvinyl group to cycloalkenones have been studied. The higher order cuprates were more reactive towards hindered enones such as 4,4- dimethylcyclohexenone and 2,4,4-trimethylcyclohexenone, and produced higher yields with the base-sensitive acetonide of cis-4,5-dihydroxycyclohexenone.en_US
dc.format.extent268580 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titlecis-2-Tri-n-butylstannylvinyl cuprates: a new synthon for the cis-1,2-ethene dianionen_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.affiliationumDepartments of Chemistry and Medicinal Chemistry,The University of Michigan, Ann Arbor, Michigan 48109 U.S.A.en_US
dc.contributor.affiliationumDepartments of Chemistry and Medicinal Chemistry,The University of Michigan, Ann Arbor, Michigan 48109 U.S.A.en_US
dc.contributor.affiliationumDepartments of Chemistry and Medicinal Chemistry,The University of Michigan, Ann Arbor, Michigan 48109 U.S.A.en_US
dc.contributor.affiliationumDepartments of Chemistry and Medicinal Chemistry,The University of Michigan, Ann Arbor, Michigan 48109 U.S.A.en_US
dc.contributor.affiliationumDepartments of Chemistry and Medicinal Chemistry,The University of Michigan, Ann Arbor, Michigan 48109 U.S.A.en_US
dc.contributor.affiliationumDepartments of Chemistry and Medicinal Chemistry,The University of Michigan, Ann Arbor, Michigan 48109 U.S.A.;Departamento de Química Universidade Federal de São Carlos-Caixa Postal 676, São Carlos, S.P.-13560- Brazilen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/30275/1/0000676.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/S0040-4039(00)77670-2en_US
dc.identifier.sourceTetrahedron Lettersen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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