6533b86efe1ef96bd12cb27a
RESEARCH PRODUCT
Carbohydrates as chiral templates: Diastereoselective Ugi synthesis of (S)-amino acids using O-acylated D-arabinopyranosylamine as the auxiliary
Wilfried SagerHorst KunzWaldemar Pfrenglesubject
chemistry.chemical_classificationGlycosylamineChemistryFormic acidStereochemistryIsocyanideOrganic ChemistryPhenylalanineBiochemistryAldehydeAmino acidchemistry.chemical_compoundDrug DiscoveryOrganic chemistryUgi reactionAliphatic compounddescription
Abstract Enantiomerically pure (S)-amino acids are synthesized via a highly diastereoselective Ugi reaction using 2,3,4-tri-O-pivaloyl-α-D-arabinopyranosylamine as the chiral template.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 1989-01-01 | Tetrahedron Letters |