| Literature DB >> 27862410 |
Kévin Renault1, Laurie-Anne Jouanno2, Antoine Lizzul-Jurse1, Pierre-Yves Renard1, Cyrille Sabot1.
Abstract
Fluorogenic reactions are largely underrepresented in the toolbox of chemoselective ligations despite their tremendous potential, particularly in chemical biology and biochemistry. In this respect, we have investigated in full detail the fluorescence behaviour of the azaphthalamide, a scaffold which is generated through a hetero-Diels-Alder reaction of 5-alkoxyoxazole and maleimide derivatives under mild conditions that are compatible with, among others, peptide chemistry. The scope and limitations of such a fluorogenic labelling strategy were examined through four distinct applications, which target enzymatic activities or bioorthogonal reactions.Entities:
Keywords: Diels-Alder; azaphthalimide; fluorescence spectroscopy; ligation; oxazole
Year: 2016 PMID: 27862410 DOI: 10.1002/chem.201603617
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236