Dansyl azide as a selective fluorescence tagging probe for click chemistry reactions and its application to monitor rasagiline in pharmacokinetic studies
Author:
Funder
toxicological research & studies center at Taibah University
Publisher
Elsevier BV
Subject
Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry
Reference19 articles.
1. Click chemistry: diverse chemical function from a few good reactions;Kolb;Angew. Chem. Int. Ed. Engl.,2001
2. Click chemistry: versatility and control in the hands of materials scientists;Nandivada;Adv. Mater.,2007
3. Click chemistry beyond metal-catalyzed cycloaddition;Becer;Angew. Chem. Int. Ed. Engl.,2009
4. Just click it: undergraduate procedures for the copper(I)-catalyzed formation of 1,2,3-triazoles from azides and terminal acetylenes;Hansen;J. Chem. Educ.,2005
5. Growing applications of “click chemistry” for bioconjugation in contemporary biomedical research;Nwe;Cancer Biother. Radiopharm.,2009
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