AU2003280995A1 - PROCESS FOR PRODUCING OPTICALLY ACTIVE Beta-AMINONITRILE COMPOUND AND AMIDE COMPOUND AS ANTIPODE THEREOF - Google Patents

PROCESS FOR PRODUCING OPTICALLY ACTIVE Beta-AMINONITRILE COMPOUND AND AMIDE COMPOUND AS ANTIPODE THEREOF

Info

Publication number
AU2003280995A1
AU2003280995A1 AU2003280995A AU2003280995A AU2003280995A1 AU 2003280995 A1 AU2003280995 A1 AU 2003280995A1 AU 2003280995 A AU2003280995 A AU 2003280995A AU 2003280995 A AU2003280995 A AU 2003280995A AU 2003280995 A1 AU2003280995 A1 AU 2003280995A1
Authority
AU
Australia
Prior art keywords
compound
antipode
optically active
producing optically
aminonitrile
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.)
Abandoned
Application number
AU2003280995A
Inventor
Noriyuki Ito
Shigeru Kawano
Yoshihiko Yasohara
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.)
Kaneka Corp
Original Assignee
Kaneka Corp
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 Kaneka Corp filed Critical Kaneka Corp
Publication of AU2003280995A1 publication Critical patent/AU2003280995A1/en
Abandoned legal-status Critical Current

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
    • C12P13/00—Preparation of nitrogen-containing organic compounds
    • C12P13/04—Alpha- or beta- amino acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00—Carboxylic acid nitriles
    • C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
    • C07C255/24—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same saturated acyclic carbon skeleton
    • C07C255/29—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the same saturated acyclic carbon skeleton containing cyano groups and acylated amino groups bound to the carbon skeleton
    • 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
    • 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
    • C12P41/007—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 acyl derivatives of racemic amines

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Zoology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Wood Science & Technology (AREA)
  • Microbiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biotechnology (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Analytical Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
AU2003280995A 2002-07-12 2003-07-11 PROCESS FOR PRODUCING OPTICALLY ACTIVE Beta-AMINONITRILE COMPOUND AND AMIDE COMPOUND AS ANTIPODE THEREOF Abandoned AU2003280995A1 (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
JP2002-204592 2002-07-12
JP2002204592 2002-07-12
JP2003-47363 2003-02-25
JP2003047363A JP2006021999A (en) 2002-07-12 2003-02-25 METHOD FOR PRODUCING OPTICALLY ACTIVE beta-AMINONITRILE COMPOUND AND ITS MIRROR IMAGE AMIDE COMPOUND
PCT/JP2003/008826 WO2004007741A1 (en) 2002-07-12 2003-07-11 PROCESS FOR PRODUCING OPTICALLY ACTIVE β-AMINONITRILE COMPOUND AND AMIDE COMPOUND AS ANTIPODE THEREOF

Publications (1)

Publication Number Publication Date
AU2003280995A1 true AU2003280995A1 (en) 2004-02-02

Family

ID=30117454

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2003280995A Abandoned AU2003280995A1 (en) 2002-07-12 2003-07-11 PROCESS FOR PRODUCING OPTICALLY ACTIVE Beta-AMINONITRILE COMPOUND AND AMIDE COMPOUND AS ANTIPODE THEREOF

Country Status (3)

Country Link
JP (1) JP2006021999A (en)
AU (1) AU2003280995A1 (en)
WO (1) WO2004007741A1 (en)

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3457294A (en) * 1966-04-22 1969-07-22 Abbott Lab N-(substituted-benzoyl) aminoaceto- and aminopropionitriles
US5597716A (en) * 1993-11-18 1997-01-28 Mitsubishi Rayon Co., Ltd. Process for producing D-lactic acid and L-lactamide
JP2000157294A (en) * 1998-11-27 2000-06-13 Kanegafuchi Chem Ind Co Ltd Production of optically active alpha-amino acid having asymmetric carbon at beta position
KR100591998B1 (en) * 2001-04-30 2006-06-22 화이자 프로덕츠 인크. Compounds useful as intermediates for 4-aminoquinoline derivatives

Also Published As

Publication number Publication date
WO2004007741A1 (en) 2004-01-22
JP2006021999A (en) 2006-01-26

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Legal Events

Date Code Title Description
MK6 Application lapsed section 142(2)(f)/reg. 8.3(3) - pct applic. not entering national phase