DE60128461D1 - Verfahren zur herstellung von optisch aktiven beta-amino alkoholen - Google Patents
Verfahren zur herstellung von optisch aktiven beta-amino alkoholenInfo
- Publication number
- DE60128461D1 DE60128461D1 DE60128461T DE60128461T DE60128461D1 DE 60128461 D1 DE60128461 D1 DE 60128461D1 DE 60128461 T DE60128461 T DE 60128461T DE 60128461 T DE60128461 T DE 60128461T DE 60128461 D1 DE60128461 D1 DE 60128461D1
- Authority
- DE
- Germany
- Prior art keywords
- active beta
- production
- optically active
- amino alcohols
- chem
- 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 - Fee Related
Links
- 230000003287 optical effect Effects 0.000 abstract 3
- 244000005700 microbiome Species 0.000 abstract 2
- 241000588771 Morganella <proteobacterium> Species 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/001—Amines; Imines
-
- 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
- C12P13/008—Preparation of nitrogen-containing organic compounds containing a N-O bond, e.g. nitro (-NO2), nitroso (-NO)
-
- 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
- C12P41/002—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by oxidation/reduction reactions
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/822—Microorganisms using bacteria or actinomycetales
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/822—Microorganisms using bacteria or actinomycetales
- Y10S435/863—Mycobacterium
- Y10S435/865—Mycobacterium fortuitum
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/822—Microorganisms using bacteria or actinomycetales
- Y10S435/874—Pseudomonas
- Y10S435/877—Pseudomonas putida
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/911—Microorganisms using fungi
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/911—Microorganisms using fungi
- Y10S435/913—Aspergillus
- Y10S435/914—Aspergillus awamori
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/911—Microorganisms using fungi
- Y10S435/913—Aspergillus
- Y10S435/917—Aspergillus niger
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S435/00—Chemistry: molecular biology and microbiology
- Y10S435/8215—Microorganisms
- Y10S435/911—Microorganisms using fungi
- Y10S435/913—Aspergillus
- Y10S435/918—Aspergillus oryzae
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Zoology (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)
- Proteomics, Peptides & Aminoacids (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000089182 | 2000-03-28 | ||
| JP2000089182 | 2000-03-28 | ||
| PCT/JP2001/001628 WO2001073100A1 (fr) | 2000-03-28 | 2001-03-02 | OBTENTION D'ALCOOLS β-AMINO OPTIQUEMENT ACTIFS |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| DE60128461D1 true DE60128461D1 (de) | 2007-06-28 |
| DE60128461T2 DE60128461T2 (de) | 2007-09-13 |
Family
ID=18604966
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE60128461T Expired - Fee Related DE60128461T2 (de) | 2000-03-28 | 2001-03-02 | Verfahren zur herstellung von optisch aktiven beta-amino alkoholen |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US6835559B2 (de) |
| EP (1) | EP1273665B1 (de) |
| KR (1) | KR100739361B1 (de) |
| CN (1) | CN1282746C (de) |
| AT (1) | ATE362543T1 (de) |
| AU (2) | AU3605701A (de) |
| CA (1) | CA2404668A1 (de) |
| CZ (1) | CZ20023202A3 (de) |
| DE (1) | DE60128461T2 (de) |
| ES (1) | ES2284620T3 (de) |
| TW (1) | TWI245801B (de) |
| WO (1) | WO2001073100A1 (de) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1371731B1 (de) * | 2001-03-02 | 2010-09-08 | Daiichi Fine Chemical Co., Ltd. | Asymmetrische aminoketon-reduktase und nukleinsäure davon |
| ATE481479T1 (de) * | 2003-10-31 | 2010-10-15 | Daiichi Fine Chem Co Ltd | Neue plasmide und deren nutzung |
| WO2007004639A1 (ja) * | 2005-07-06 | 2007-01-11 | Daiichi Fine Chemical Co., Ltd. | 光学活性エリスロ-β-アミノアルコールの製法 |
| WO2007097106A1 (ja) * | 2006-02-24 | 2007-08-30 | Kao Corporation | 新規微生物、当該新規微生物を用いたドデカヒドロ-3a,6,6,9a-テトラメチルナフト[2,1-b]フラン中間体の製造方法 |
| EP2004836A1 (de) * | 2006-04-13 | 2008-12-24 | DSMIP Assets B.V. | Verfahren zur darstellung eines enantiomerenangereicherten beta-aminoalkohols aus glycin und einem aldehyd in gegenwart einer threonin-aldolase und einer decarboxylase |
| CN101117640B (zh) * | 2007-07-20 | 2011-06-15 | 浙江大学 | D-氨基酸的生物催化制备方法 |
| CN110824092A (zh) * | 2018-08-08 | 2020-02-21 | 天津药物研究院有限公司 | 一种s-3-氨基-3-苯基丙醇异构体的手性检测方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4237304A (en) * | 1978-10-26 | 1980-12-02 | The Dow Chemical Company | Oxazolinium salts and method of preparation |
| US4879233A (en) * | 1989-02-10 | 1989-11-07 | Schering Corporation | Novel Aspergillus niveus microorganism used for the chiral reduction of carbonyl groups |
| US5629200A (en) * | 1993-11-18 | 1997-05-13 | Daicel Chemical Industries, Ltd. | Production of optically active 2-amino-1-phenylethanol derivatives by asymetrical assimilation |
| JP3529904B2 (ja) | 1995-06-19 | 2004-05-24 | 鐘淵化学工業株式会社 | 光学活性1−ハロ−3−アミノ−4−フェニル−2−ブタノール誘導体の製造法 |
| WO1998012155A1 (en) | 1996-09-18 | 1998-03-26 | Shionogi & Co., Ltd. | Process for preparing optically acitve alcohol by reduction with asymmetric borane |
| JPH10248591A (ja) | 1997-03-06 | 1998-09-22 | Sumitomo Chem Co Ltd | 光学活性アルコールの製造方法 |
-
2001
- 2001-03-02 DE DE60128461T patent/DE60128461T2/de not_active Expired - Fee Related
- 2001-03-02 CA CA002404668A patent/CA2404668A1/en not_active Abandoned
- 2001-03-02 EP EP01908255A patent/EP1273665B1/de not_active Expired - Lifetime
- 2001-03-02 CZ CZ20023202A patent/CZ20023202A3/cs unknown
- 2001-03-02 AU AU3605701A patent/AU3605701A/xx active Pending
- 2001-03-02 US US10/240,056 patent/US6835559B2/en not_active Expired - Fee Related
- 2001-03-02 CN CNB018073808A patent/CN1282746C/zh not_active Expired - Fee Related
- 2001-03-02 AT AT01908255T patent/ATE362543T1/de not_active IP Right Cessation
- 2001-03-02 TW TW090104939A patent/TWI245801B/zh not_active IP Right Cessation
- 2001-03-02 ES ES01908255T patent/ES2284620T3/es not_active Expired - Lifetime
- 2001-03-02 WO PCT/JP2001/001628 patent/WO2001073100A1/ja not_active Ceased
- 2001-03-02 AU AU2001236057A patent/AU2001236057B2/en not_active Ceased
- 2001-03-02 KR KR1020027012721A patent/KR100739361B1/ko not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| DE60128461T2 (de) | 2007-09-13 |
| CA2404668A1 (en) | 2002-09-26 |
| EP1273665A4 (de) | 2006-04-05 |
| EP1273665A1 (de) | 2003-01-08 |
| KR100739361B1 (ko) | 2007-07-18 |
| AU3605701A (en) | 2001-10-08 |
| CN1420935A (zh) | 2003-05-28 |
| TWI245801B (en) | 2005-12-21 |
| US20040091981A1 (en) | 2004-05-13 |
| KR20030022103A (ko) | 2003-03-15 |
| WO2001073100A1 (fr) | 2001-10-04 |
| AU2001236057B2 (en) | 2006-03-02 |
| US6835559B2 (en) | 2004-12-28 |
| CZ20023202A3 (cs) | 2003-03-12 |
| CN1282746C (zh) | 2006-11-01 |
| ES2284620T3 (es) | 2007-11-16 |
| EP1273665B1 (de) | 2007-05-16 |
| ATE362543T1 (de) | 2007-06-15 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| PT960944E (pt) | Producao melhorada de taxol e de taxanos por culturas de celulas da especie taxus | |
| ATE429414T1 (de) | Verfahren zur herstellung von organischen carbonaten | |
| DE69937272D1 (de) | Verfahren zur herstellung eines peptids mittels eines hilfspeptids | |
| DE60226243D1 (de) | Peptidsynthasegen, peptidsynthase und verfahren zur herstellung eines dipeptids | |
| DE602004008183D1 (de) | Verfahren zur Herstellung von L-Cystein unter Verwendung eines zur Gattung Escherichia gehörenden Bakteriums | |
| ATE426021T1 (de) | Verfahren zur herstellung von biopterinen | |
| ATE404689T1 (de) | Verfahren zur herstellung von optisch aktiven aminoalkoholen | |
| DE60128461D1 (de) | Verfahren zur herstellung von optisch aktiven beta-amino alkoholen | |
| DE60041171D1 (de) | Verfahren zur herstellung eines fermentationsproduktes | |
| ATE428730T1 (de) | Verfahren zur herstellung einer alpha-1- antitrypsinlösung | |
| DE60017375D1 (de) | Verfahren zur herstellung eines diols | |
| ATE407130T1 (de) | Verfahren zur herstellung von 2- azetidinonderivaten | |
| ECSP055803A (es) | Ésteres de ácido carbámico con actividad anticolinérgica | |
| ATE216725T1 (de) | Verfahren zur herstellung von l-isoleucin durch fermentation und l-homoserine als einzige stickstoffquelle | |
| ATE397088T1 (de) | Verfahren zur herstellung von (s)- oder (r)-3,3,3-trifluor-2-hydroxy-2-methylpropionsaü e | |
| BRPI0416274A (pt) | método para produzir solução de amÈnio de ácido orgánico | |
| DE60334468D1 (de) | Verfahren zur herstellung von theanin | |
| ATE258603T1 (de) | Verfahren zur herstellung von pravastatin und lovastatin | |
| DE602004022639D1 (de) | Verfahren zur herstellung von lactonase und nutzung davon | |
| ATE439333T1 (de) | Verfahren zur herstellung optisch aktiver propoxyanilinderivate | |
| EP1298119A4 (de) | Chlorhydroxyaceton-derivate und verfahren zur herstellung optisch aktiver chlorpropandiol-derivate aus diesen chlorhydroxyaceton-derivaten | |
| DE602006009010D1 (de) | Verfahren zur Herstellung von beta-Hydroxy-Aminosäuren und dafür geeignetes Enzym | |
| DE59905165D1 (de) | Verfahren zur Herstellung von Orthoestern | |
| ATE279527T1 (de) | Verfahren zur herstellung von l-2- aminoadipinsäure | |
| DE602005002146D1 (de) | Verfahren zur mikrobiologischen Herstellung von optisch aktiven 3-Chlor-2-methyl-1,2-propandiol |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8364 | No opposition during term of opposition | ||
| 8339 | Ceased/non-payment of the annual fee |