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Amino Acids ; 47(5): 899-907, 2015 May.
Article in English | MEDLINE | ID: mdl-25618753

ABSTRACT

Racemic-protected α-ethynylphenylalanine was synthesized from DL-2-benzylserine using α-benzylserinal as key intermediate and was successfully resolved by HPLC on a chiral stationary phase at a semipreparative scale. The absolute configuration of both enantiomers was determined by vibrational circular dichroism.


Subject(s)
Alanine/analogs & derivatives , Benzyl Compounds/chemistry , Serine/analogs & derivatives , Alanine/chemical synthesis , Circular Dichroism , Molecular Conformation , Serine/chemistry , Stereoisomerism
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