SG120094A1 - Process for the enzymatic preparation of enantiomerically enriched beta-amino acids - Google Patents

Process for the enzymatic preparation of enantiomerically enriched beta-amino acids

Info

Publication number
SG120094A1
SG120094A1 SG200302193A SG200302193A SG120094A1 SG 120094 A1 SG120094 A1 SG 120094A1 SG 200302193 A SG200302193 A SG 200302193A SG 200302193 A SG200302193 A SG 200302193A SG 120094 A1 SG120094 A1 SG 120094A1
Authority
SG
Singapore
Prior art keywords
amino acids
alkyl
enantiomerically enriched
beta
optionally substituted
Prior art date
Application number
SG200302193A
Inventor
Harald Dr Groger
Helge Werner
Original Assignee
Degussa
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 Degussa filed Critical Degussa
Publication of SG120094A1 publication Critical patent/SG120094A1/en

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

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Microbiology (AREA)
  • General Chemical & Material Sciences (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)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

Production of enantiomerically enriched, N-unprotected beta-amino acids (I) comprises enzymatic hydrolysis of an enantiomeric mixture of N-unprotected beta-aminoacid esters (II) using a hydrolase, provided that (II) is other than a methyl or ethyl ester. An Independent claim is also included for new beta-aminoacid n-propyl esters of formula (II'). R = 1-8C alkyl, 2-8C alkenyl, 2-8C alkynyl, 3-8C cycloalkyl (optionally substituted by 1-3 1-8C alkyl), 6-18C aryl (optionally substituted by 1-3 1-8C alkyl), 7-19C aralkyl, 3-18C heteroaryl (optionally substituted by 1-3 1-8C alkyl) or 4-19C heteroaralkyl; and R' = H or as defined for R.
SG200302193A 2002-05-08 2003-04-14 Process for the enzymatic preparation of enantiomerically enriched beta-amino acids SG120094A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE10220739A DE10220739A1 (en) 2002-05-08 2002-05-08 Process for the enzymatic preparation of enantiomerically enriched β-amino acids

Publications (1)

Publication Number Publication Date
SG120094A1 true SG120094A1 (en) 2006-03-28

Family

ID=29225124

Family Applications (1)

Application Number Title Priority Date Filing Date
SG200302193A SG120094A1 (en) 2002-05-08 2003-04-14 Process for the enzymatic preparation of enantiomerically enriched beta-amino acids

Country Status (14)

Country Link
EP (1) EP1361279B1 (en)
JP (1) JP4386670B2 (en)
KR (1) KR101172905B1 (en)
CN (1) CN1260364C (en)
AT (1) ATE332391T1 (en)
CA (1) CA2428059C (en)
DE (3) DE10220739A1 (en)
DK (1) DK1361279T3 (en)
ES (1) ES2268212T3 (en)
HR (1) HRP20030357A2 (en)
IL (1) IL155785A0 (en)
PT (1) PT1361279E (en)
SG (1) SG120094A1 (en)
SI (1) SI1361279T1 (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4270991B2 (en) 2002-10-11 2009-06-03 株式会社リコー Information recording apparatus, information recording method, information recording program, storage medium storing information recording program, and information recording system
JP4591347B2 (en) * 2003-03-17 2010-12-01 宇部興産株式会社 3-Amino-3-arylpropionic acid n-alkyl ester and process for producing the same, and optically active 3-amino-3-arylpropionic acid and process for producing enantiomers thereof
FR2853327B1 (en) * 2003-04-04 2012-07-27 Solvay PROCESS FOR THE PRODUCTION OF ENANTIOPOR BETA-AMINOACID DERIVATIVES AND ENANTIOPA BETA-AMINOACIDIC DERIVATIVES
JP4361094B2 (en) 2003-12-10 2009-11-11 エボニック デグサ ゲーエムベーハー Method for producing enantiomerically enriched amino acids
WO2005095325A1 (en) * 2004-03-03 2005-10-13 Degussa Ag PROCESS FOR THE PREPARATION OF β-AMINOCARBOXYLIC ACIDS
WO2006038698A1 (en) * 2004-10-08 2006-04-13 Ube Industries, Ltd. PROCESS FOR PRODUCTION OF OPTICALLY ACTIVE (S)- OR (R)-β-AMINO ACIDS AND OPTICALLY ACTIVE (R)- OR (S)-β-AMINO ACID ESTERS, 2-ALKOXYETHYL ESTERS OF β-AMINO ACIDS, AND OPTICALLY ACITVE (S)- OR (R)-2-ALKOXYETHYL ESTERS OF β-AMINO ACIDS
CN101180402A (en) * 2005-05-17 2008-05-14 宇部兴产株式会社 Process for production of carboxylic acid using surfactant-modifying enzyme
SG11201403306RA (en) * 2011-12-19 2014-12-30 Sumitomo Chemical Co METHOD FOR PRODUCING OPTICALLY-ACTIVE α-SUBSTITUTED-β-AMINO ACID

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4439524A (en) * 1979-07-07 1984-03-27 Bayer Aktiengesellschaft Stereoselective resolution of phenylglycine derivatives with enzyme resins
US4636470A (en) * 1984-08-17 1987-01-13 Stauffer Chemical Company Resolution of racemates of amino acids

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5552317A (en) * 1995-05-26 1996-09-03 Industrial Technology Research Institute Method for preparing optically active homophenylalanine and esters thereof using lipase from wheat germ or Candida lipolytica
CA2384191A1 (en) * 1999-08-31 2001-03-08 Benjamin M. Skead Enantiomerically-enriched compounds having photocleavable bond(s) and methods related thereto

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4439524A (en) * 1979-07-07 1984-03-27 Bayer Aktiengesellschaft Stereoselective resolution of phenylglycine derivatives with enzyme resins
US4636470A (en) * 1984-08-17 1987-01-13 Stauffer Chemical Company Resolution of racemates of amino acids

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
TETRAHEDRON LETTERS. VOL. 41, 2000, PAGES 2697-2681 *

Also Published As

Publication number Publication date
IL155785A0 (en) 2003-12-23
PT1361279E (en) 2006-11-30
SI1361279T1 (en) 2006-12-31
DE10320211A1 (en) 2004-02-12
DE50304116D1 (en) 2006-08-17
ES2268212T3 (en) 2007-03-16
KR20030087565A (en) 2003-11-14
DE10220739A1 (en) 2003-11-27
ATE332391T1 (en) 2006-07-15
CN1456675A (en) 2003-11-19
JP2003325195A (en) 2003-11-18
EP1361279A1 (en) 2003-11-12
CA2428059C (en) 2011-08-02
CA2428059A1 (en) 2003-11-08
HRP20030357A2 (en) 2004-04-30
KR101172905B1 (en) 2012-08-10
JP4386670B2 (en) 2009-12-16
DK1361279T3 (en) 2006-11-06
CN1260364C (en) 2006-06-21
EP1361279B1 (en) 2006-07-05

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