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The Synthesis and Borohydride Reduction of some Alloxazine Derivatives
dc.contributor.authorMüller, Franzen_US
dc.contributor.authorDudley, Kenneth H.en_US
dc.date.accessioned2006-04-28T16:33:36Z
dc.date.available2006-04-28T16:33:36Z
dc.date.issued1971en_US
dc.identifier.citationMÜller, Franz; Dudley, Kenneth H. (1971)."The Synthesis and Borohydride Reduction of some Alloxazine Derivatives." Helvetica Chimica Acta 54(5): 1487-1497. <http://hdl.handle.net/2027.42/37969>en_US
dc.identifier.issn0018-019Xen_US
dc.identifier.issn1522-2675en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/37969
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=5121754&dopt=citationen_US
dc.description.abstractUnequivocal syntheses of N(1 or 3)-mono-substituted 7, 8-dimethylalloxazines are described. The borohydride reduction of various alloxazines has been studied under aerobic and anaerobic conditions, in the absence of light. These reactions are discussed in relation to other work on 7, 8-dimethylisoalloxazines (flavins) and on certain flavoproteins.en_US
dc.format.extent637325 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherWILEY-VCH Verlag GmbHen_US
dc.subject.otherChemistryen_US
dc.subject.otherOrganic Chemistryen_US
dc.titleThe Synthesis and Borohydride Reduction of some Alloxazine Derivativesen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Biological Chemistry, The University of Michigan Medical School, Ann Arbor, Michigan 48104 ; Center for Research in Pharmacology and Toxicology, The School of Medicine, The University of North Carolina, Chapel Hill, North Carolina 27514 ; Recipient of a Research Career Development Award, K4-GM-42, 599; from the National Institutes of Health, U. S. Public Health Service.en_US
dc.contributor.affiliationumDepartment of Biological Chemistry, The University of Michigan Medical School, Ann Arbor, Michigan 48104 ; Center for Research in Pharmacology and Toxicology, The School of Medicine, The University of North Carolina, Chapel Hill, North Carolina 27514en_US
dc.identifier.pmid5121754en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/37969/1/19710540534_ftp.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1002/(ISSN)1522-2675en_US
dc.identifier.sourceHelvetica Chimica Actaen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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