ASYMMETRIC-SYNTHESIS OF (2S,3S)-2,3-DIAMINOBUTANOIC AND (2R,3S)-2,3-DIAMINOBUTANOIC ACIDS, NONPROTEIN AMINO-ACID DIASTEREOMERS FOUND IN A NUMBER OF PEPTIDE ANTIBIOTICS
Aj. Burke et al., ASYMMETRIC-SYNTHESIS OF (2S,3S)-2,3-DIAMINOBUTANOIC AND (2R,3S)-2,3-DIAMINOBUTANOIC ACIDS, NONPROTEIN AMINO-ACID DIASTEREOMERS FOUND IN A NUMBER OF PEPTIDE ANTIBIOTICS, Synlett, (7), 1996, pp. 621
(2S,3S)- and (2R,3S)-2,3-diaminobutanoic acids (DABA) are uncommon, na
turally occurring amino acid diastereomers found as components of a nu
mber of peptide antibiotics. These 2,3-diamino acids have been synthes
ised by direct and indirect routes, with addition of a chiral lithium
amide to tert-butyl crotonate as a key step.