The synthesis of 5-(alditol-1-C-yl)-hydantoin derivatives was performed via diastereoselective aldol-type addition of 1,3- dibenzyl-hydantoin to enantiopure aldehydo sugars. Starting from the D-ribo-configured 5-(alditol-1-C-yl)-hydantoin template, the synthesis of (2R,3S,4R)-3,4,5-trihydroxynorvaline was carried out.

Diastereoselective synthesis of 5-(alditol-1-C-yl)-hydantoins and their use as precursors of polyhydroxylated a-amino acids

Ulgheri F;Crisma M;Spanu P
2004

Abstract

The synthesis of 5-(alditol-1-C-yl)-hydantoin derivatives was performed via diastereoselective aldol-type addition of 1,3- dibenzyl-hydantoin to enantiopure aldehydo sugars. Starting from the D-ribo-configured 5-(alditol-1-C-yl)-hydantoin template, the synthesis of (2R,3S,4R)-3,4,5-trihydroxynorvaline was carried out.
2004
Istituto di Chimica Biomolecolare - ICB - Sede Pozzuoli
Istituto di Chimica Biomolecolare - ICB - Sede Pozzuoli
Hydantoin
Imidazolidin-2
4-dione
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/164923
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