dc.contributor.author | SENGE, MATHIAS | |
dc.date.accessioned | 2010-06-15T11:53:21Z | |
dc.date.available | 2010-06-15T11:53:21Z | |
dc.date.issued | 1993 | |
dc.date.submitted | 1993 | en |
dc.identifier.citation | E. 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 - 874 | en |
dc.identifier.other | Y | |
dc.identifier.uri | http://hdl.handle.net/2262/40140 | |
dc.description | PUBLISHED | en |
dc.description.abstract | Base-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.sponsorship | We 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.extent | 872 | en |
dc.format.extent | 874 | en |
dc.language.iso | en | en |
dc.publisher | Royal Society of Chemistry | en |
dc.relation.ispartofseries | Journal of the Chemical Society, Chemical Communications; | |
dc.rights | Y | en |
dc.subject | Chemistry | en |
dc.title | A Novel 2,18-Bridged Biliverdin Derivative | en |
dc.type | Journal Article | en |
dc.type.supercollection | scholarly_publications | en |
dc.type.supercollection | refereed_publications | en |
dc.identifier.peoplefinderurl | http://people.tcd.ie/sengem | |
dc.identifier.rssinternalid | 29196 | |
dc.identifier.rssuri | http://dx.doi.org/10.1039/C39930000872 | en |
dc.contributor.sponsor | Deutsche Forschungsgemeinschaft (DFG) | en |