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Bommarius et al., 1992 - Google Patents

Operational Stability of Enzymes: Acylase‐Catalyzed Resolution of N‐Acetyl Amino Acids to Enantiomerically Pure l‐Amino Acids

Bommarius et al., 1992

Document ID
4421303993460269633
Author
Bommarius A
Drauz K
Klenk H
Wandrey C
Publication year
Publication venue
Annals of the New York Academy of Sciences

External Links

Snippet

Enantiomerically pure L-amino acids are interesting compounds in parenteral nutrition (infusion solutions), as feed and food additives, as intermediates for pharmaceuticals, cosmetics, and pesticides, and as chiral synthons for organic synthesis. L-Amino acids can …
Continue reading at nyaspubs.onlinelibrary.wiley.com (other versions)

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    • C12P13/00—Preparation of nitrogen-containing organic compounds
    • C12P13/04—Alpha- or beta- amino acids
    • C12P13/22—Tryptophan; Tyrosine; Phenylalanine; 3,4-Dihydroxyphenylalanine
    • C12P13/222—Phenylalanine
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    • C12P13/00—Preparation of nitrogen-containing organic compounds
    • C12P13/02—Amides, e.g. chloramphenicol or polyamides; Imides or polyimides; Urethanes, i.e. compounds comprising N-C=O structural element or polyurethanes
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    • C12P41/00—Processes using enzymes or micro-organisms to separate optical isomers from a racemic mixture
    • C12P41/006—Processes using enzymes or micro-organisms to separate optical isomers from a racemic mixture by reactions involving C-N bonds, e.g. nitriles, amides, hydantoins, carbamates, lactames, transamination reactions, or keto group formation from racemic mixtures
    • C12P41/007—Processes using enzymes or micro-organisms to separate optical isomers from a racemic mixture by reactions involving C-N bonds, e.g. nitriles, amides, hydantoins, carbamates, lactames, transamination reactions, or keto group formation from racemic mixtures by reactions involving acyl derivatives of racemic amines
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    • C12P21/00—Preparation of peptides or proteins
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