4.6 Article

Synthesis of Porphyrin, Chlorin and Phthalocyanine Derivatives by Azide-Alkyne Click Chemistry

Journal

CURRENT MEDICINAL CHEMISTRY
Volume 22, Issue 28, Pages 3217-3254

Publisher

BENTHAM SCIENCE PUBL LTD
DOI: 10.2174/0929867322666150716115832

Keywords

Click chemistry; Huisgen's cycloaddition; photodynamic therapy; photosensitizers; therapeutic

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The aim of this review is to provide a summary of the use of copper-catalyzed azide-alkyne cycloaddition (CuAAC) in the synthesis of porphyrin, chlorin and phthalocyanine derivatives for different types of therapeutic applications. The click reaction is a powerful and versatile tool for scientists working on the synthesis of various symmetrically and asymmetrically substituted tetrapyrrolic derivatives. For example, click chemistry is widely used for the elaboration of photosensitizer conjugates for photodynamic therapy applications. Other biological applications are also described.

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