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Biosynthesis of phenolic tetrahydroisoquinoline alkaloids of peyote
dc.contributor.authorKhanna, K. L.en_US
dc.contributor.authorTakido, M.en_US
dc.contributor.authorRosenberg, Harryen_US
dc.contributor.authorPaul, Ara G.en_US
dc.date.accessioned2006-04-17T15:09:12Z
dc.date.available2006-04-17T15:09:12Z
dc.date.issued1970-08en_US
dc.identifier.citationKhanna, K. L., Takido, M., Rosenberg, H., Paul, A. G. (1970/08)."Biosynthesis of phenolic tetrahydroisoquinoline alkaloids of peyote." Phytochemistry 9(8): 1811-1815. <http://hdl.handle.net/2027.42/32728>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6TH7-42H2T1N-19/2/195d2c35fce50d4e80d928203e1089b3en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/32728
dc.description.abstractData are presented supporting a proposed pathway of biosynthesis of the phenolic tetrahydroisoquinoline alkaloids of peyote from dopamine. It is suggested that meta-O-methylation of dopamine, hydroxylation in the 5-position, para-O-methylation and finally cyclizations yield anhalamine, anhalidine, anhalonidine and pellotine.en_US
dc.format.extent419920 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleBiosynthesis of phenolic tetrahydroisoquinoline alkaloids of peyoteen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumCollege of Pharmacy, The University of Michigan, Ann Arbor, Mi. 48104, U.S.A.en_US
dc.contributor.affiliationumCollege of Pharmacy, The University of Michigan, Ann Arbor, Mi. 48104, U.S.A.en_US
dc.contributor.affiliationumCollege of Pharmacy, The University of Michigan, Ann Arbor, Mi. 48104, U.S.A.en_US
dc.contributor.affiliationumCollege of Pharmacy, The University of Michigan, Ann Arbor, Mi. 48104, U.S.A.en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/32728/1/0000096.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/S0031-9422(00)85597-1en_US
dc.identifier.sourcePhytochemistryen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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