1. Syntheses of [2-13C] and [1,2-13C] labelled α-ketoglutaric acid. Jack E. Baldwin, Robert M. Adlington, Mark A. Russell, Christopher J. Schofield, Mark E. Wood. Journal of Labelled Compounds and Radiopharmaceuticals, Volume 27, Issue 9, pages 1091–1099, September 1989
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http://dx.doi.org/10.1002/jlcr.25802709142. A practical laboratory route to the synthesis of trideuteriomethyl-[13C] iodide. Gregory S. Coumbarides, Jason Eames, Neluka Weerasooriya. Journal of Labelled Compounds and Radiopharmaceuticals, Volume 46, Issue 4, pages 291–296, 30 March 2003
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http://dx.doi.org/10.1002/jlcr.6663. Ring-opening copolymerization of 2-aryl-1-methylenecyclopropanes with carbon monoxide initiated by Pd-bpy complexes. Kim, Sunwook; Takeuchi, Daisuke; Osakada, Kohtaro. Macromolecular Chemistry and Physics (2003), 204(4), 666-673.
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http://dx.doi.org/10.1002/macp.200390035pentacoordinate carbon species. Forbus, T. R., Jr.; Martin, J. C. Heteroatom Chemistry (1993), 4(2-3), 129-36.
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http://dx.doi.org/10.1002/hc.520040205[1-11C](2H3) and [2-11C](2H3) acetate for in vivo studies of myocardium using PET. Kihlberg, Tor; Valind, Sven; Laangstroem, Bengt.
Nuclear Medicine and Biology (1994), 21(8), 1067-72.
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http://dx.doi.org/10.1016/0969-8051(94)90178-3