Abstract
By taking advantage of the reversibility of the thermolysin-catalysed amide synthesis-hydrolysis reaction on a solid support, both L,L and L,D diastereoisomers of dipeptides and L-amino acids are accessible in good yields starting from enantiomeric mixtures of amino acids.
Original language | English |
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Pages (from-to) | 621-622 |
Number of pages | 2 |
Journal | Organic and Biomolecular Chemistry |
Volume | 1 |
Issue number | 4 |
Early online date | 28 Jan 2003 |
DOIs | |
Publication status | Published - 21 Feb 2003 |
Keywords
- enzymatic optical resolution
- acylation-hydrolysis
- solid support