deals with azodyes naturalisedthroughglycoconjugation with a very common saccharide – lactose – and with its galactose and glucose components. The conjugation takes place through a bifunctional linker, here a terminal dibromoalkane, so the final products are very stable diether derivatives of the starting dyes. These transformations produce naturaliseddyes – indeed, water-soluble and multipurpose
Synthesis of Glycoconjugated Phthalonitriles for New Phthalocyanine-Based Photosensitizers
作者:Göran Crucius、Michael Hanack、Thomas Ziegler
DOI:10.1080/07328303.2015.1050106
日期:2015.6.13
glycoconjugated phthalocyanines in photodynamic therapy. In this study we describe the concise synthesis and full characterization of 16 differently 3,6-bisglycoconjugated phthalonitriles 3, 5, 6, 8, and 48–59, which are precursors for a new generation of photosensitizers, namely, nonperipheral glycoconjugated phthalocyanines. The first example for the synthesis of a nonperipheral glycoconjugated zinc phthalocyanine