Parker, 2001 - Google Patents
Dynamic kinetic resolution of [alpha]-substituted carboxylic acid derivativesParker, 2001
- Document ID
- 8080857676314395889
- Author
- Parker R
- Publication year
- Publication venue
- PQDT-UK & Ireland
External Links
Snippet
Dynamic resolution exists where a resolution takes place under conditions in which racemisation of the substrate occurs. This overcomes many of the major drawbacks of traditional resolution and allows a single enantiomer to be obtained in a theoretically …
- 150000001732 carboxylic acid derivatives 0 title description 8
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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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- C12P13/04—Alpha- or beta- amino acids
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- C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
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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
- C12P41/005—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 carboxylic acid groups in the enantiomers or the inverse reaction
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- C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
- C12P17/16—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms containing two or more hetero rings
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- C07C231/18—Preparation of optical isomers by stereospecific synthesis
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- C07C229/28—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being saturated and containing rings
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- C07C271/06—Esters of carbamic acids
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- C12P7/00—Preparation of oxygen-containing organic compounds
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