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An Operationally Simple and Efficient Synthesis of Orthogonally Protected L-threo-β-Hydroxyasparagine

A synthesis of orthogonally protected L-threo-β-hydroxyasparagine from L-aspartic acid is reported. Iodocyclization of 3-benzoylaminoaspartic acid provided an intermediate oxazoline dicarboxylate that was efficiently hydrolyzed to L-threo-β-hydroxyaspartic acid. The synthetic route for conversion of...

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Detalhes bibliográficos
Main Authors: Guzmán-Martinez, Aikomari, VanNieuwenhze, Michael S.
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2707822/
https://ncbi.nlm.nih.gov/pubmed/19593390
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1055/s-2007-982544
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