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Pure Appl. Chem., 1981, Vol. 53, No. 6, pp. 1215-1232

http://dx.doi.org/10.1351/pac198153061215

Application of CMR spectroscopy to the study of porphyrin and corrin biosynthesis in vitro and in vivo

A. I. Scott

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  • Santos Ana Filipa L.O.M., Ribeiro da Silva Manuel A.V.: Reprint of: Energetics and molecular structure of alkyl 1-methylpyrrolecarboxylates (alkyl=methyl or ethyl). The Journal of Chemical Thermodynamics 2014. <http://dx.doi.org/10.1016/j.jct.2014.03.018>
  • Santos Ana Filipa L. O. M., Ribeiro da Silva Manuel A. V.: The influence of methyl groups on the torsion angle and on the energetics of 1-phenylpyrrole derivatives: a thermodynamic and computational study. Struct Chem 2013, 24, 1981. <http://dx.doi.org/10.1007/s11224-013-0288-z>
  • Santos Ana Filipa L.O.M., Ribeiro da Silva Manuel A.V.: Energetics and molecular structure of alkyl 1-methylpyrrolecarboxylates (alkyl=methyl or ethyl). The Journal of Chemical Thermodynamics 2013, 67, 190. <http://dx.doi.org/10.1016/j.jct.2013.08.004>
  • Santos Ana Filipa L. O. M., Ribeiro da Silva Manuel A. V.: Molecular Energetics of Alkyl Pyrrolecarboxylates: Calorimetric and Computational Study. J. Phys. Chem. A 2013, 117, 5195. <http://dx.doi.org/10.1021/jp4032628>
  • Santos Ana Filipa L.O.M., Ribeiro da Silva Manuel A.V.: Molecular energetics of pyrrolecarbonitriles and derivatives: A combined calorimetric and computational study. K J CHEM THERMODYN 2012, 48, 194. <http://dx.doi.org/10.1016/j.jct.2011.12.019>
  • Haldar Pranab, Ray Jayanta K: Chemoselective reduction of a lactam carbonyl group in the presence of a gem-dicarboxylate by sodium borohydride and iodine: a facile entry to N-aryl trisubstituted pyrroles. Tetrahetron Lett 2003, 44, 8229. <http://dx.doi.org/10.1016/j.tetlet.2003.09.085>
  • Adamczyk Maciej, Fishpaugh Jeffrey R., Heuser Kevin J., Ramp John M., Reddy Rajarathnam E., Wong Martin: Synthesis of immunocomponents for the measurement of lead (Pb) by fluorescence polarization immunoassay. Tetrahedron 1998, 54, 3093. <http://dx.doi.org/10.1016/S0040-4020(98)00060-X>
  • Adamczyk Maciej, Reddy Rajarathnam E.: A new methodology for the preparation of 2-cyanopyrroles and synthesis of porphobilinogen. Tetrahedron 1996, 52, 14689. <http://dx.doi.org/10.1016/0040-4020(96)00941-6>
  • Adamczyk Maciej, Reddy Rajarathnam E.: A convenient synthesis of 2-Cyanopyrroles from isocyanoacetonitrile. Tetrahetron Lett 1995, 36, 7983. <http://dx.doi.org/10.1016/0040-4039(95)01724-V>
  • Adamczyk Maciej, Reddy Rajarathnam E.: A convenient and versatile synthesis of porphobilinogen. Tetrahetron Lett 1995, 36, 9121. <http://dx.doi.org/10.1016/0040-4039(95)01979-R>
  • Krivdin Leonid B., Della Ernest W.: Spin—spin coupling constants between carbons separated by more than one bond. Progr Nucl Magn Reson Spectrosc 1991, 23, 301. <http://dx.doi.org/10.1016/0079-6565(91)80004-L>
  • Kurumaya Katsuyuki, Okazaki Takeo, Seido Nobuo, Akasaka Yuzuru, Kawajiri Yoshiki, Kajiwara Masahiro, Kondo Masao: A facile synthesis of δ-aminolevulinic acid (ALA) regioselectively labeled with 13C and direct observation of enzymatic transformation from ALA to porphobilinogen (PBG). J Lab Compds Radiopharm 1989, 27, 217. <http://dx.doi.org/10.1002/jlcr.2580270212>
  • Krivdin Leonid B., Kalabin Gennady A.: Structural applications of one-bond carboncarbon spin—spin coupling constants. Progr Nucl Magn Reson Spectrosc 1989, 21, 293. <http://dx.doi.org/10.1016/0079-6565(89)80007-X>
  • Evans J. N. S., Fagerness P. E., Mackenzie N. E., Scott A. I.: 1H,3H and13C NMR studies on porphobilinogen. Magn Reson Chem 1985, 23, 939. <http://dx.doi.org/10.1002/mrc.1260231112>
  • Horak R. Marthinus, Steyn Pieter S., Vleggaar Robert: Carbon—carbon coupling constants derived from biosynthetic studies. Magn Reson Chem 1985, 23, 995. <http://dx.doi.org/10.1002/mrc.1260231204>
  • Pfaltz Andreas, Anwar Saeed: Synthesis of α-aminoketones via selective reduction of acyl cyanides. Tetrahetron Lett 1984, 25, 2977. <http://dx.doi.org/10.1016/S0040-4039(01)81341-1>