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Ex Post Glycoconjugation of Phthalocyanines

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posted on 2010-06-04, 00:00 authored by Herwig J. Berthold, Stephan Franke, Joachim Thiem, Theo Schotten
For the first time, fully fledged phthalocyanines (Pcs) were ex post glycoconjugated, that is, via 1,3-dipolar cycloaddition reaction. This divergent approach gains rapid access to a broad range of highly diverse Pcs bearing chemically sensitive substituents. This will be a breakthrough in generating structure−activity relationships (SAR) for the development of novel bioactive molecules.

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