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dc.contributor.authorSENGE, MATHIAS
dc.date.accessioned2010-06-15T11:53:21Z
dc.date.available2010-06-15T11:53:21Z
dc.date.issued1993
dc.date.submitted1993en
dc.identifier.citationE. D. Sturrock, J. D. Bull, R. E. Kirsch, R. K. Pandey, M. O. Senge, K. M. Smith, A Novel 2,18-Bridged Biliverdin Derivative, Journal of the Chemical Society, Chemical Communications, 1993, 872 - 874en
dc.identifier.otherY
dc.identifier.urihttp://hdl.handle.net/2262/40140
dc.descriptionPUBLISHEDen
dc.description.abstractBase-catalysed dehydrohalogenation of a 3,18-bis(2-chloroethyl)biliverdin 1 affords a novel 3-vinylbiliverdin 3 in which the 2- and 18-positions are bridged with a propano-tether; the structure of 3 has been established using single crystal X-ray and 1H nuclear Overhauser effect studies.en
dc.description.sponsorshipWe thank H. Spies, who kindly performed the NOE experiments. This research was supported by grants from the National Institutes of Health (HL 22252) and the S. A. Medical Research Council.en
dc.format.extent872en
dc.format.extent874en
dc.language.isoenen
dc.publisherRoyal Society of Chemistryen
dc.relation.ispartofseriesJournal of the Chemical Society, Chemical Communications;
dc.rightsYen
dc.subjectChemistryen
dc.titleA Novel 2,18-Bridged Biliverdin Derivativeen
dc.typeJournal Articleen
dc.contributor.sponsorDeutsche Forschungsgemeinschaft (DFG)en
dc.type.supercollectionscholarly_publicationsen
dc.type.supercollectionrefereed_publicationsen
dc.identifier.peoplefinderurlhttp://people.tcd.ie/sengem
dc.identifier.rssinternalid29196
dc.identifier.rssurihttp://dx.doi.org/10.1039/C39930000872en


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