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A Very Short Route to Enantiomerically Pure Coumarin-Bearing Fluorescent Amino Acids

Abstract : No bulkier than a tryptophan or a tyrosine residue are the fluorescent coumaryl amino acids described. These building blocks can be synthesized rapidly with high enantiomeric purity and introduced readily into a peptidic sequence. Their fluorescence properties allow, for example, the investigation of the cellular localization of labeled peptides through confocal fluorescence microscopy
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https://hal-normandie-univ.archives-ouvertes.fr/hal-02385514
Contributor : Laurent Bischoff <>
Submitted on : Thursday, November 28, 2019 - 6:52:41 PM
Last modification on : Thursday, July 30, 2020 - 3:13:45 AM

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Marie-Priscille Brun, Laurent Bischoff, Christiane Garbay. A Very Short Route to Enantiomerically Pure Coumarin-Bearing Fluorescent Amino Acids. Angewandte Chemie International Edition, Wiley-VCH Verlag, 2004, 43 (26), pp.3432-3436. ⟨10.1002/anie.200454116⟩. ⟨hal-02385514⟩

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