Literature DB >> 27862410

Fluorogenic Behaviour of the Hetero-Diels-Alder Ligation of 5-Alkoxyoxazoles with Maleimides and their Applications.

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.
© 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

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


  1 in total

1.  Fluorophore-Assisted Click Chemistry through Copper(I) Complexation.

Authors:  Victor Flon; Magalie Bénard; Damien Schapman; Ludovic Galas; Pierre-Yves Renard; Cyrille Sabot
Journal:  Biomolecules       Date:  2020-04-16
  1 in total

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