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  • 13C MAS NMR  (1)
  • 1H NMR  (1)
  • Biochemistry and Biotechnology  (1)
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  • 1
    ISSN: 1573-5079
    Keywords: 13C MAS NMR ; EPR ; FTIR ; spheroidene ; stable isotope labelling ; ubiquinone
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract In this minireview the information at the atomic level that has been obtained by studying photosynthetic reaction centers with site-directed isotope labelling is discussed. The required isotopically labelled RCs are prepared using isotopically labelled amino acids and cofactors that have been prepared via organic total synthetic chemistry. In some cases the results of isotopically labelled RCs that are prepared via other methods are also discussed.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Journal of Peptide Science 3 (1997), S. 193-208 
    ISSN: 1075-2617
    Keywords: peptaibol ; antibiotic ; peptide synthesis ; NMR spectroscopy ; mass spectrometry ; isotope labelling ; Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: For the first time the total synthesis of the peptaibol antibiotic zervamicin IIB is described. Synthesis of this peptaibol was achieved by the Fmoc/tert-butyl strategy in solution using a fragment condensation approach. Three fragments of zervamicin IIB were obtained by stepwise elongation with Fmoc amino acids using BOP as a coupling reagent. For the introduction of the highly sterically hindered α-aminoisobutyric acid residues BOP/DMAP activation was applied. The Fmoc group was removed by reaction with 0.1 M NaOH in dioxane/methanol/water (30/9/1, v/v/v). Peptide fragments were coupled by means of a new coupling reagent, CF3-PyBOP. Using the strategy developed, zervamicin IIB and two analogues specifically deuterium-labelled at different positions of the glutamine-11 residue have been synthesized in 40% overall yield based on the isotopically labelled amino acid and with 98±2% of isotope enrichment. FAB mass spectroscopy, 600 MHz 1H-NMR spectroscopy and high-performance liquid chromatography provided convincing evidence that the synthetic products, zervamicin IIB and its deuterium-labelled analogues, fully correspond to the naturally occurring zervamicin IIB. © 1997 European Peptide Society and John Wiley & Sons, Ltd.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Liebigs Annalen 1999 (1999), S. 2909-2914 
    ISSN: 1434-193X
    Keywords: Methyl methacrylate ; 13C label ; Mass spectrometry ; 1H NMR ; 13C NMR ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A synthetic scheme has been developed to prepare methyl methacrylate specifically 13C-labelled at all different positions and in any combination of positions, from simple, commercially available starting materials. According to this scheme methyl (1-13C)- and methyl (2-13C)methacrylate (1a and 1b) have been prepared with high label incorporation (99%).
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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