par Monclus, Michel
;Masson, Carine;Luxen, André 
Référence Journal of fluorine chemistry, 70, 1, page (39-43)
Publication Publié, 1995-01


Référence Journal of fluorine chemistry, 70, 1, page (39-43)
Publication Publié, 1995-01
Article révisé par les pairs
Résumé : | A convenient asymmetric synthesis of (2S)-2-amino-3-(2-fluoro-5-hydroxyphenyl) propanoic acid, (2S)-2-amino-3-(4-fluoro-3-hydroxyphenyl) propanoic acid and (2S)-2-amino-3-(2-fluoro-4-hydroxyphenyl) propanoic acid is described. Key steps include the synthesis of the benzyl bromides, the alkylation of the glycine enolate derivative ((S)-Boc-BMI) and the hydrolysis of the alkylated Boc-BMI. © 1995. |