ES2039366T3 - Procedimiento para la resolucion enzimatica de 2-amino-1-alcanoles racemicos. - Google Patents
Procedimiento para la resolucion enzimatica de 2-amino-1-alcanoles racemicos.Info
- Publication number
- ES2039366T3 ES2039366T3 ES198787104586T ES87104586T ES2039366T3 ES 2039366 T3 ES2039366 T3 ES 2039366T3 ES 198787104586 T ES198787104586 T ES 198787104586T ES 87104586 T ES87104586 T ES 87104586T ES 2039366 T3 ES2039366 T3 ES 2039366T3
- Authority
- ES
- Spain
- Prior art keywords
- alcanols
- amino
- racemic
- procedure
- formula
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
- C12P41/006—Processes using enzymes or microorganisms 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
- C12P41/008—Processes using enzymes or microorganisms 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 carbamates
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Zoology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Genetics & Genomics (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Microbiology (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Analytical Chemistry (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Immobilizing And Processing Of Enzymes And Microorganisms (AREA)
- Enzymes And Modification Thereof (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
SE DESCRIBE UN PROCEDIMIENTO PARA LA RESOLUCION ENZIMATICA DE 2-AMINO-1-ALCANOLES RACEMICOS DE FORMULA (I) EN LA QUE R REPRESENTA UN GRUPO ALQUILO DE 1 A 8 C, QUE COMPRENDE LA HIDROLISIS ENZIMATICA DE DERIVADOS DE ESTERES N-ALCOXICARBONILICOS RACEMICOS (R,S) DE DICHOS 2-AMINO-1-ALCANOLES RACEMICOS (I), QUE TIENEN LA FORMULA (II) EN LA QUE R" QUE TIENE EL MISMO SIGNIFICADO QUE R Y R'' REPRESENTA UN GRUPO ALQUILO DE 1 A 8 C O UN GRUPO BENCILO, EN PRESENCIA DE UNA ENZIMA, PREFERIBLEMENTE UNA LIPASA CAPAZ DE HIDROLIZAR SELECTIVAMENTE (ASIMETRICAMENTE) EL ISOMERO (R) DEL ESTER (II), QUEDANDO INALTERADO EL ISOMERO (S), DESPUES DE LO CUAL SE LLEVA A CABO LA SEPARACION E HIDROLISIS USUAL DE LOS PRODUCTOS DE LA HIDROLISIS ENZIMATICA A LOS CORRESPONDIENTES 2-AMINO-ALCANOLES (R)* Y (S) POR SEPARADO, DE FORMULA (I). LOS 2-AMINO-1-ALCANOLES OPTICAMENTE ACTIVOS OBTENIDOS PUEDEN EMPLEARSE COMO PRODUCTOS INTERMEDIOS PARA LA PRODUCCION DE PRODUCTOS BIOLOGICAMENTE ACTIVOS.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT19944/86A IT1188641B (it) | 1986-03-28 | 1986-03-28 | Processo per la risoluzione enzimatica di 2-ammino-1-alcanoli racemi |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2039366T3 true ES2039366T3 (es) | 1993-10-01 |
Family
ID=11162539
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES198787104586T Expired - Lifetime ES2039366T3 (es) | 1986-03-28 | 1987-03-27 | Procedimiento para la resolucion enzimatica de 2-amino-1-alcanoles racemicos. |
Country Status (13)
| Country | Link |
|---|---|
| EP (1) | EP0239122B1 (es) |
| JP (1) | JPS62275697A (es) |
| KR (1) | KR870009028A (es) |
| AT (1) | ATE77412T1 (es) |
| AU (1) | AU585703B2 (es) |
| BR (1) | BR8701422A (es) |
| DE (1) | DE3779785T2 (es) |
| ES (1) | ES2039366T3 (es) |
| IL (1) | IL82034A0 (es) |
| IN (1) | IN165472B (es) |
| IT (1) | IT1188641B (es) |
| MA (1) | MA20921A1 (es) |
| ZA (1) | ZA872093B (es) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8911456D0 (en) * | 1989-05-18 | 1989-07-05 | Earl & Wright Ltd | Locating arrangement |
| US5300437A (en) * | 1989-06-22 | 1994-04-05 | Celgene Corporation | Enantiomeric enrichment and stereoselective synthesis of chiral amines |
| US4950606A (en) * | 1989-06-22 | 1990-08-21 | Celgene Corporation | Enantiomeric enrichment and stereoselective synthesis of chiral amines |
| US5169780A (en) * | 1989-06-22 | 1992-12-08 | Celgene Corporation | Enantiomeric enrichment and stereoselective synthesis of chiral amines |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT1191638B (it) * | 1985-10-31 | 1988-03-23 | Montedison Spa | Processo per la separazione enzimatica degli isomeri ottici del 2-amminobutanolo |
-
1986
- 1986-03-28 IT IT19944/86A patent/IT1188641B/it active
-
1987
- 1987-03-23 ZA ZA872093A patent/ZA872093B/xx unknown
- 1987-03-25 IN IN231/CAL/87A patent/IN165472B/en unknown
- 1987-03-25 AU AU70633/87A patent/AU585703B2/en not_active Ceased
- 1987-03-25 JP JP62069279A patent/JPS62275697A/ja active Pending
- 1987-03-25 KR KR870002752A patent/KR870009028A/ko not_active Withdrawn
- 1987-03-27 IL IL82034A patent/IL82034A0/xx not_active IP Right Cessation
- 1987-03-27 BR BR8701422A patent/BR8701422A/pt not_active Application Discontinuation
- 1987-03-27 DE DE8787104586T patent/DE3779785T2/de not_active Expired - Lifetime
- 1987-03-27 EP EP87104586A patent/EP0239122B1/en not_active Expired - Lifetime
- 1987-03-27 MA MA21162A patent/MA20921A1/fr unknown
- 1987-03-27 AT AT87104586T patent/ATE77412T1/de not_active IP Right Cessation
- 1987-03-27 ES ES198787104586T patent/ES2039366T3/es not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| EP0239122A3 (en) | 1988-09-14 |
| JPS62275697A (ja) | 1987-11-30 |
| EP0239122A2 (en) | 1987-09-30 |
| AU7063387A (en) | 1987-10-01 |
| IN165472B (es) | 1989-10-28 |
| IT1188641B (it) | 1988-01-20 |
| IT8619944A0 (it) | 1986-03-28 |
| MA20921A1 (fr) | 1987-10-01 |
| BR8701422A (pt) | 1988-01-05 |
| KR870009028A (ko) | 1987-10-22 |
| AU585703B2 (en) | 1989-06-22 |
| EP0239122B1 (en) | 1992-06-17 |
| ATE77412T1 (de) | 1992-07-15 |
| ZA872093B (en) | 1987-09-14 |
| DE3779785D1 (de) | 1992-07-23 |
| DE3779785T2 (de) | 1992-12-10 |
| IT8619944A1 (it) | 1987-09-28 |
| IL82034A0 (en) | 1987-10-20 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG2A | Definitive protection |
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