GB2031896B - Process for the optical resolution of d,l-2-amino-4-methylphosphinobutyric acid - Google Patents

Process for the optical resolution of d,l-2-amino-4-methylphosphinobutyric acid

Info

Publication number
GB2031896B
GB2031896B GB7933176A GB7933176A GB2031896B GB 2031896 B GB2031896 B GB 2031896B GB 7933176 A GB7933176 A GB 7933176A GB 7933176 A GB7933176 A GB 7933176A GB 2031896 B GB2031896 B GB 2031896B
Authority
GB
United Kingdom
Prior art keywords
amino
optical resolution
methylphosphinobutyric acid
methylphosphinobutyric
acid
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
Application number
GB7933176A
Other languages
English (en)
Other versions
GB2031896A (en
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Meiji Seika Kaisha Ltd
Original Assignee
Meiji Seika Kaisha Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Meiji Seika Kaisha Ltd filed Critical Meiji Seika Kaisha Ltd
Publication of GB2031896A publication Critical patent/GB2031896A/en
Application granted granted Critical
Publication of GB2031896B publication Critical patent/GB2031896B/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12PFERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P13/00Preparation of nitrogen-containing organic compounds
    • C12P13/04Alpha- or beta- amino acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/30Phosphinic acids [R2P(=O)(OH)]; Thiophosphinic acids ; [R2P(=X1)(X2H) (X1, X2 are each independently O, S or Se)]
    • C07F9/301Acyclic saturated acids which can have further substituents on alkyl
    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/14Hydrolases (3)
    • C12N9/78Hydrolases (3) acting on carbon to nitrogen bonds other than peptide bonds (3.5)
    • C12N9/80Hydrolases (3) acting on carbon to nitrogen bonds other than peptide bonds (3.5) acting on amide bonds in linear amides (3.5.1)

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Zoology (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Genetics & Genomics (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Molecular Biology (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • General Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
GB7933176A 1978-10-02 1979-09-25 Process for the optical resolution of d,l-2-amino-4-methylphosphinobutyric acid Expired GB2031896B (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12039078A JPS5547630A (en) 1978-10-02 1978-10-02 Optical resolution of phosphorus-containing amino acid

Publications (2)

Publication Number Publication Date
GB2031896A GB2031896A (en) 1980-04-30
GB2031896B true GB2031896B (en) 1983-03-23

Family

ID=14785011

Family Applications (1)

Application Number Title Priority Date Filing Date
GB7933176A Expired GB2031896B (en) 1978-10-02 1979-09-25 Process for the optical resolution of d,l-2-amino-4-methylphosphinobutyric acid

Country Status (4)

Country Link
JP (1) JPS5547630A (zh)
DE (1) DE2939269C2 (zh)
FR (1) FR2438054A1 (zh)
GB (1) GB2031896B (zh)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3048612C2 (de) * 1980-12-23 1982-12-02 Hoechst Ag, 6000 Frankfurt "Verfahren zur enzymatischen Trennung von L-2-Ami no-4-methylphosphinobuttersäure"
JPS59219297A (ja) * 1983-05-27 1984-12-10 Meiji Seika Kaisha Ltd 光学活性な〔(3−アミノ−3−カルボキシ)プロピル−1〕−ホスフイン酸誘導体の製造法
DE3544376A1 (de) * 1985-12-14 1987-06-19 Hoechst Ag Dipeptide mit c-terminalem phosphinothricin, verfahren zu ihrer herstellung und ihre verwendung zur bekaempfung unerwuenschten pflanzenwuchses
JPH0518339Y2 (zh) * 1987-05-11 1993-05-17
DE3724722A1 (de) * 1987-07-25 1989-02-16 Hoechst Ag Verbessertes verfahren zur enzymatischen herstellung von l-2-amino-4-methylphosphinobuttersaeure
DE3817191A1 (de) * 1988-05-20 1989-11-30 Hoechst Ag Verfahren zur racemisierung von optisch aktiver d-2-n-phenacetylamino-4- methylphosphinobuttersaeure
DE3842025A1 (de) * 1988-12-14 1990-07-05 Hoechst Ag Verfahren zur herstellung von l-phosphinothricin
DE3903446A1 (de) * 1989-02-06 1990-10-18 Hoechst Ag Verfahren zur enzymatischen trennung von 2-amino-4-methylphosphinobuttersaeurederivaten
EP0499376A1 (en) * 1991-01-31 1992-08-19 Hoechst Celanese Corporation Precipitation-induced asymmetric transformation of chiral alpha-amino acids and salts thereof
DE4422045A1 (de) * 1994-06-26 1996-01-04 Hoechst Schering Agrevo Gmbh Verfahren zur enzymatischen Spaltung von 2-Amino-4-methylphosphinobutansäureamid-Derivaten
US6235516B1 (en) 1996-04-25 2001-05-22 Novartis Ag Biocatalysts with amine acylase activity
DE19933362A1 (de) * 1999-07-20 2001-02-08 Aventis Cropscience Gmbh Verfahren zur Herstellung von L-Aminosäuren aus ihren racemischen N-Acetyl-D,L-Derivaten durch enzymatische Racemat-Spaltung mittels isolierter, rekombinanter Enzyme
EP2287322A1 (en) * 2002-02-26 2011-02-23 Syngenta Limited A method of selectively producing male or female sterile plants

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3816254A (en) * 1970-02-03 1974-06-11 Tanabe Seiyaku Co Optical resolution of racemic amino acids
JPS5318006B2 (zh) * 1973-09-28 1978-06-13
FR2352827A1 (fr) * 1976-05-26 1977-12-23 Rhone Poulenc Ind Complexes support-aminoacylase

Also Published As

Publication number Publication date
JPS6247520B2 (zh) 1987-10-08
JPS5547630A (en) 1980-04-04
FR2438054A1 (fr) 1980-04-30
DE2939269C2 (de) 1982-07-08
DE2939269A1 (de) 1980-04-30
FR2438054B1 (zh) 1985-02-15
GB2031896A (en) 1980-04-30

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PG Patent granted