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Furanverbindungen, 7. Mitt.: Synthese linear anellierter Furoxanthone

  • Organic Chemistry and Biochemistry
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Zusammenfassung

Die bemerkenswerte photodynamische Wirkung linear anellierter Furobenzopyrone (Psoralen, Methylpsoralen und Khellin) wird zum Anlaß für die Synthese von Xanthonanalogen des 8-Methylpsoralens, wie z. B. des 2,11-Dimethyl- oder des 2,7,11-Trimethyl-5-oxo-5H-furo[3,2-b]xanthens genommen.

Abstract

The appreciable photodynamic activity of linear furanobenzopyrones (psoralen, methyl psoralen and khellin) is discussed. The synthesis of xanthone analogues of 8-methylpsoralen viz. 2,11-dimethyl- or 2,7,11-trimethyl-5-oxo-5H-furo[3,2-b]xanthenes is recorded.

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Teilveröffentlichung der vonY. S. Agasimundin eingereichten Dissertation zur Erlangung eines Dr. phil. der Karnatak University.

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Agasimundin, Y.S., Rajagopal, S. Furanverbindungen, 7. Mitt.: Synthese linear anellierter Furoxanthone. Monatshefte für Chemie 97, 423–428 (1966). https://doi.org/10.1007/BF00905260

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  • DOI: https://doi.org/10.1007/BF00905260

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