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Non-biomimetic route to deoxyadenosine adducts of carcinogenic polycyclic aromatic hydrocarbons
dc.contributor.authorJin Kim, Seongen_US
dc.contributor.authorHarris, Constance M.en_US
dc.contributor.authorJung, Kee-Yongen_US
dc.contributor.authorKoreeda, Masatoen_US
dc.contributor.authorHarris, Thomas M.en_US
dc.date.accessioned2006-04-10T14:33:16Z
dc.date.available2006-04-10T14:33:16Z
dc.date.issued1991-10-21en_US
dc.identifier.citationJin Kim, Seong, Harris, Constance M., Jung, Kee-Yong, Koreeda, Masato, Harris,, Thomas M. (1991/10/21)."Non-biomimetic route to deoxyadenosine adducts of carcinogenic polycyclic aromatic hydrocarbons." Tetrahedron Letters 32(43): 6073-6076. <http://hdl.handle.net/2027.42/29083>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6THS-431C18F-19/2/3cf3277eaa9b558d4b7c3d98a90aa2fden_US
dc.identifier.urihttps://hdl.handle.net/2027.42/29083
dc.description.abstractAminotriols are prepared by direct aminolysis of the diol epoxides of polycyclic aromatic hydrocarbons, providing a substantial improvement over literature methods. The condensation of aminotriols with 6-halopurine deoxyribonucleosides provides a regio- and stereospecific synthesis of deoxyadenosine N6 adducts.en_US
dc.format.extent276755 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleNon-biomimetic route to deoxyadenosine adducts of carcinogenic polycyclic aromatic hydrocarbonsen_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.affiliationotherDepartment of Chemistry and Center in Molecular Toxicology, Vanderbilt University, Nashville, TN 37235; USAen_US
dc.contributor.affiliationotherDepartment of Chemistry and Center in Molecular Toxicology, Vanderbilt University, Nashville, TN 37235; USAen_US
dc.contributor.affiliationotherDepartment of Chemistry and Center in Molecular Toxicology, Vanderbilt University, Nashville, TN 37235; USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/29083/1/0000118.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0040-4039(91)80756-Ven_US
dc.identifier.sourceTetrahedron Lettersen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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