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   <subfield code="a">10.1007/BF00812322</subfield>
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   <subfield code="a">(NATIONALLICENCE)springer-10.1007/BF00812322</subfield>
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   <subfield code="a">On the nature of &quot;soluble” hypericin in Hypericum species</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Heinz Falk, Wolfgang Schmitzberger]</subfield>
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   <subfield code="a">Zur Natur des &quot;löslichen&quot; Hypericins in Hypericum -Arten</subfield>
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   <subfield code="a">Summary: The two red and two violet &quot;soluble” pigments ofHypericum species were isolated by means of extraction, chromatography, and counter-current droplet chromatography. In contrast to authentic hypericin, they are soluble in common organic solvents and even in water. Using NMR experiments it was deduced that hypericin, pseudohypericin, protohypericin, and protopseudohypericin are present in the plant as their rapidly interconverting 3- and 4-phenolate ions. From AAS the main counter-ion of these phenolates was derived to be potassium. The potassium and N-ethyl-N,N-diisopropylammonium salts of hypericin were synthesizcd for comparison. A preparative procedure to isolate hypericin and pseudohypericin from plant material was developed.</subfield>
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   <subfield code="a">Springer-Verlag, 1992</subfield>
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   <subfield code="a">&quot;Soluble” Hypericin</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Hypericin-, Pseudohypericin-, Protohypericin-, Protopseudohypericin-, Potassium salts</subfield>
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   <subfield code="a">1H-NMR</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">13C-NMR</subfield>
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   <subfield code="a">Droplet counter-current chromatography</subfield>
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   <subfield code="a">Hypericum perforatum L</subfield>
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   <subfield code="u">Institut für Chemie, Johannes-Kepler-Universität Linz, A-4040, Linz, Austria</subfield>
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   <subfield code="t">Monatshefte für Chemie / Chemical Monthly</subfield>
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   <subfield code="g">123/8-9(1992-08-01), 731-739</subfield>
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