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Direct analysis of mushroom constituents by mass spectrometry

✍ Scribed by G.A. McClusky; R.G. Cooks; A.M. Knevel


Publisher
Elsevier Science
Year
1978
Tongue
French
Weight
226 KB
Volume
19
Category
Article
ISSN
0040-4039

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✦ Synopsis


New mass spectrometric methodology' for structural elucidation of components present in complex mixtures is here applied to a species of mushroom, Helvella esculenta. This approach is shown to have the following characteristics which are important in natural products chemistry: (i) no preparation of the biological material is required, (ii) extremely small samples suffice, (iii) highly specific structure-related information is obtained for each natural product CH $H=N /CH3 N CH$H=N N /CH3 'CH2NH2 'CH20H respectively. Since the geminal aminohydrazine, 3_, and the hydroxyhydrazine, 5, are not IJO. a6 typically stable, they probably correspond to the gas phase reaction of N-methylacetaldehydrazone with formaldehyde or methylimine. It is less likely that Kwas derived by pyrolysis or a gas phase reaction. This preliminary result raises interesting questions regarding the biogenesis of azomethine technique in studying Acknowledgment: References -p canpounds and provides further evidence of the usefulness of the MIKES natural products.


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## Abstract This review is focused on the capillary electrophoresis‐mass spectrometric (CE‐MS) analysis of nucleic acid constituents in the broadest sense, going from nucleotides and adducted nucleotides over nucleoside analogues to oligonucleotides. These nucleic acid constituents play an importan