Highly enantioselective synthesis of a fluorescent amino acid

Add time:09/03/2019    Source:sciencedirect.com

A high enantiomeric excess (>99.5%) synthesis of l-2-amino-3-(7-methoxy-4-coumaryl) propionic acid (l-Amp) is described. The two step synthesis route of this non-proteinogenic amino acid includes an oxazinone derivative as glycine enolate, which is alkylated with the fluorogenic group.

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