Ahmed et al., 2012 - Google Patents
Applications of enzymatic and non-enzymatic methods to access enantiomerically pure compounds using kinetic resolution and racemisationAhmed et al., 2012
View PDF- Document ID
- 15866956229094705906
- Author
- Ahmed M
- Kelly T
- Ghanem A
- Publication year
- Publication venue
- Tetrahedron
External Links
Snippet
The augmented awareness of the importance of chirality and its strong association with biological activity created an immense need for development of enantiomerically pure compounds at a reduced cost. The global sales of chiral technology products in 2008 were …
- 150000001875 compounds 0 title abstract description 17
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- C12P41/00—Processes using enzymes or micro-organisms to separate optical isomers from a racemic mixture
- C12P41/003—Processes using enzymes or micro-organisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
- C12P41/004—Processes using enzymes or micro-organisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions by esterification of alcohol- or thiol groups in the enantiomers or the inverse reaction
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- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
- C12P7/04—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
- C12P7/16—Butanols
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- 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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