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Syntheses,Photochemical Properties,and Tautomerism of Intramolecularly Friedel-Crafts Acylated Hypericin Derivatives
Authors:Mario?Waser,Yulita?Popova,Christoph?Etzlstorfer,Werner F.?Huber,Heinz?Falk  author-information"  >  author-information__contact u-icon-before"  >  mailto:heinz.falk@jku.at"   title="  heinz.falk@jku.at"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author
Affiliation:(1) Institute of Organic Chemistry, Johannes Kepler University Linz, A-4040 Linz, Austria;(2) Institute for Chemical Technology of Organic Materials, Johannes Kepler University Linz, A-4040 Linz, Austria
Abstract:Summary. Intramolecularly Friedel-Crafts acylation carried out on the hypericin moiety provided a new class of 9,12-dicarbonyl substituted hypericin derivatives as potential candidates for photodynamic therapy (PDT). Focusing on cyclopentanone and cyclohexanone condensed derivatives, investigations concerning the chemical and photochemical properties as well as the tautomerism of these compounds were performed.
Keywords:. Phenanthroperylenequinones   Semiempirical calculations   Anthraquinones   Photodynamic therapy.
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