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A convenient synthesis of -(5'-deoxy-5'-adenosyl)- (+/-) -2-methylhomocysteine
dc.contributor.authorRamalingam, Kondareddiaren_US
dc.contributor.authorWoodard, Ronald W.en_US
dc.date.accessioned2006-04-07T19:16:13Z
dc.date.available2006-04-07T19:16:13Z
dc.date.issued1985en_US
dc.identifier.citationRamalingam, Kondareddiar, Woodard,, Ronald W. (1985)."A convenient synthesis of -(5'-deoxy-5'-adenosyl)- (+/-) -2-methylhomocysteine." Tetrahedron Letters 26(9): 1135-1136. <http://hdl.handle.net/2027.42/25930>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6THS-42HXXV4-2NG/2/85d18fac07a72cef295e587284acc2e7en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/25930
dc.description.abstractThe synthesis of -(5'-deoxy-5'-adenosyl)-+-2-methylhomocysteine in two steps from +--2-methylmethionine is described.en_US
dc.format.extent109988 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleA convenient synthesis of -(5'-deoxy-5'-adenosyl)- (+/-) -2-methylhomocysteineen_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 Medicinal Chemistry, College of Pharmacy, University of Michigan, Ann Arbor, Michigan 48109-1065 U.S.A.en_US
dc.contributor.affiliationumDepartment of Medicinal Chemistry, College of Pharmacy, University of Michigan, Ann Arbor, Michigan 48109-1065 U.S.A.en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/25930/1/0000493.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/S0040-4039(00)98415-6en_US
dc.identifier.sourceTetrahedron Lettersen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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