The third generation of glycoconjugated azo dyes (GADs) was prepared linking monoazo dyes to 6-amino-6-deoxy-d-galactose or 6'-amino-6'-deoxylactose through mixed amido-ester connections. The complementary conjugation reactions were studied using the succinyl derivative of either the acetal protected aminosugar or the azodye. Target “naturalized” GADs were obtained after acid hydrolysis of the acetal protecting groups present on the sugar moiety.

A New Generation of Glycoconjugated Azo Dyes Based on Aminosugars

GUAZZELLI, LORENZO;CATELANI, GIORGIO;D'ANDREA, FELICIA
2015-01-01

Abstract

The third generation of glycoconjugated azo dyes (GADs) was prepared linking monoazo dyes to 6-amino-6-deoxy-d-galactose or 6'-amino-6'-deoxylactose through mixed amido-ester connections. The complementary conjugation reactions were studied using the succinyl derivative of either the acetal protected aminosugar or the azodye. Target “naturalized” GADs were obtained after acid hydrolysis of the acetal protecting groups present on the sugar moiety.
2015
Guazzelli, Lorenzo; Catelani, Giorgio; D'Andrea, Felicia
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11568/757866
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