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

Citation
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
Citations number
23
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
09365214
Issue
7
Year of publication
1996
Database
ISI
SICI code
0936-5214(1996):7<621:AO(A(>2.0.ZU;2-E
Abstract
(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.