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A Route to Amino Functionalized Hypericin Derivatives and their Chemical and Photochemical Properties Pertaining to Photodynamic Therapy
Authors:Bernd?Lackner,Klaus?Bretterbauer,Clemens?Schwarzinger,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, 4040 Linz, Austria;(2) Institute for Chemical Technology of Organic Materials, Johannes Kepler University, 4040 Linz, Austria
Abstract:Summary. Syntheses of amino functionalized hypericin derivatives could be achieved starting from the recently prepared emodin derived 1,3,8-trimethoxy-6-amino-9,10-anthraquinone. Our strategies for the preparation of 10,11-didemethyl-10,11-diaminohypericin, 10,11-didemethyl-10,11-di(acetylamino) hypericin, and its hypericinoidic diazepine derivative include synthetical modifications on the levels of the anthraquinone, anthron, and the phenanthroperylenequinone system itself. The chemical as well as photochemical properties of these unique hypericin derivatives, which might constitute new photodynamic therapy agents, are reported.
Keywords:. Anthraquinones   Anthrons   Microwave assisted synthesis   Phenanthroperylenequinones   Seven-membered ring closure.
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