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Müller, K. ; Mayer, K. K. ; Wiegrebe, Wolfgang

¹O₂-Oxidation of Dithranol to Chrysazin

Müller, K., Mayer, K. K. and Wiegrebe, Wolfgang (1986) ¹O₂-Oxidation of Dithranol to Chrysazin. Archiv der Pharmazie 319, pp. 1009-1018.

Date of publication of this fulltext: 06 Jul 2010 08:45
Article
DOI to cite this document: 10.5283/epub.15661


Abstract

Raab's biochemically active species, derived from dithranol (1), is the anion 1a (Sect. A), which is a photosensitizer. Its sensitizing potency is quantitatively compared with that of rose bengal, tetraphenylporphyrine and other sensitizers (Sect. B). In Sect. C the mechanism of the conversion of 1a with 1Δg1802 to chrysazin (2) is elucidated. Raab's biochemisch aktives Dithranol(l)-Derivat ...

Raab's biochemically active species, derived from dithranol (1), is the anion 1a (Sect. A), which is a photosensitizer.
Its sensitizing potency is quantitatively compared with that of rose bengal, tetraphenylporphyrine
and other sensitizers (Sect. B). In Sect. C the mechanism of the conversion of 1a with 1Δg1802 to
chrysazin (2) is elucidated.

Raab's biochemisch aktives Dithranol(l)-Derivat ist dessen Anion la, das zugleich ein Photosensibilisator
ist (Abschn. A). Die Sensibilisatorstärke von 1a wird quantitativ mit der von Bengalrosa und Tetraphenylporphyrin
u. a. verglichen (Abschn. B). In Abschn. C wird der Reaktionsmechanismus der Umsetzung
von 1 zu Chrysazin (2) mit Hilfe von 1Δg1802 geklärt.


Involved Institutions


Details

Item typeArticle
Journal or Publication TitleArchiv der Pharmazie
Publisher:John Wiley & Sons
Volume:319
Page Range:pp. 1009-1018
Date1986
InstitutionsChemistry and Pharmacy > Institute of Pharmacy > Alumni or Retired Professors > Prof. Wiegrebe
Dewey Decimal Classification500 Science > 540 Chemistry & allied sciences
StatusPublished
RefereedYes, this version has been refereed
Created at the University of RegensburgUnknown
URN of the UB Regensburgurn:nbn:de:bvb:355-epub-156619
Item ID15661

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