A Very Short Route to Enantiomerically Pure Coumarin-Bearing Fluorescent Amino Acids - Normandie Université Access content directly
Journal Articles Angewandte Chemie International Edition Year : 2004

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

Dates and versions

hal-02385514 , version 1 (28-11-2019)

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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, 2004, 43 (26), pp.3432-3436. ⟨10.1002/anie.200454116⟩. ⟨hal-02385514⟩
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