DE69016851T2 - Verfahren zur Herstellung von S-2,2-R1,R2-1,3-Dioxolan-4-methanol. - Google Patents

Verfahren zur Herstellung von S-2,2-R1,R2-1,3-Dioxolan-4-methanol.

Info

Publication number
DE69016851T2
DE69016851T2 DE69016851T DE69016851T DE69016851T2 DE 69016851 T2 DE69016851 T2 DE 69016851T2 DE 69016851 T DE69016851 T DE 69016851T DE 69016851 T DE69016851 T DE 69016851T DE 69016851 T2 DE69016851 T2 DE 69016851T2
Authority
DE
Germany
Prior art keywords
dioxolane
methanol
preparation
microorganism
subjecting
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
Application number
DE69016851T
Other languages
English (en)
Other versions
DE69016851D1 (de
Inventor
Smet Marie Jose De
Boer Lex De
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.)
Shell Internationale Research Maatschappij BV
Original Assignee
Shell Internationale Research Maatschappij BV
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 Shell Internationale Research Maatschappij BV filed Critical Shell Internationale Research Maatschappij BV
Application granted granted Critical
Publication of DE69016851D1 publication Critical patent/DE69016851D1/de
Publication of DE69016851T2 publication Critical patent/DE69016851T2/de
Anticipated expiration legal-status Critical
Expired - Fee Related 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
    • C12P17/00Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/02Oxygen as only ring hetero atoms
    • C12P17/04Oxygen as only ring hetero atoms containing a five-membered hetero ring, e.g. griseofulvin, vitamin C
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D317/00Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/10Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
    • C07D317/14Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D317/18Radicals substituted by singly bound oxygen or sulfur atoms
    • C07D317/20Free hydroxyl or mercaptan
    • 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
    • C12P41/00Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • C12P41/001Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by metabolizing one of the enantiomers
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00Chemistry: molecular biology and microbiology
    • Y10S435/8215Microorganisms
    • Y10S435/822Microorganisms using bacteria or actinomycetales
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00Chemistry: molecular biology and microbiology
    • Y10S435/8215Microorganisms
    • Y10S435/911Microorganisms using fungi
    • YGENERAL 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00Chemistry: molecular biology and microbiology
    • Y10S435/8215Microorganisms
    • Y10S435/911Microorganisms using fungi
    • Y10S435/912Absidia

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Zoology (AREA)
  • Wood Science & Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Genetics & Genomics (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Biotechnology (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Microbiology (AREA)
  • Analytical Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)
  • Steroid Compounds (AREA)
  • Polyurethanes Or Polyureas (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Dental Preparations (AREA)
DE69016851T 1989-06-29 1990-06-27 Verfahren zur Herstellung von S-2,2-R1,R2-1,3-Dioxolan-4-methanol. Expired - Fee Related DE69016851T2 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP89201733 1989-06-29

Publications (2)

Publication Number Publication Date
DE69016851D1 DE69016851D1 (de) 1995-03-23
DE69016851T2 true DE69016851T2 (de) 1995-07-13

Family

ID=8202425

Family Applications (1)

Application Number Title Priority Date Filing Date
DE69016851T Expired - Fee Related DE69016851T2 (de) 1989-06-29 1990-06-27 Verfahren zur Herstellung von S-2,2-R1,R2-1,3-Dioxolan-4-methanol.

Country Status (15)

Country Link
US (1) US4956285A (de)
EP (1) EP0405691B1 (de)
JP (1) JPH03117496A (de)
AT (1) ATE118551T1 (de)
AU (1) AU643689B2 (de)
CA (1) CA2020197A1 (de)
DD (1) DD296922A5 (de)
DE (1) DE69016851T2 (de)
FI (1) FI903314A0 (de)
IE (1) IE902366A1 (de)
IL (1) IL94898A (de)
NO (1) NO902881L (de)
NZ (1) NZ234296A (de)
PT (1) PT94527A (de)
ZA (1) ZA905112B (de)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL8902035A (nl) * 1989-08-09 1991-03-01 Stamicarbon Enantioselectieve bereiding van s-2r1,2r2-1,3-dioxolaan-4-methanol en derivaten daarvan.
US8349777B2 (en) * 2010-11-22 2013-01-08 Chevron Oronite Company Llc Lubricating composition containing 1,3-dioxolane-4-methanol compounds as antiwear additives

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4575558A (en) * 1984-02-15 1986-03-11 American Hospital Supply Corporation Preparation of optically active 1,3-dioxolane-4-methanol compounds
IL82416A0 (en) 1986-05-08 1987-11-30 Gist Brocades Nv Process for the preparation of r-2,2-r1,r2-1,3-dioxolane-4-methanol

Also Published As

Publication number Publication date
EP0405691A1 (de) 1991-01-02
IE902366L (en) 1990-12-29
IE902366A1 (en) 1991-06-19
EP0405691B1 (de) 1995-02-15
IL94898A0 (en) 1991-04-15
AU5796590A (en) 1991-01-03
IL94898A (en) 1994-07-31
CA2020197A1 (en) 1990-12-30
AU643689B2 (en) 1993-11-25
NO902881L (no) 1991-01-02
US4956285A (en) 1990-09-11
NO902881D0 (no) 1990-06-28
ZA905112B (en) 1991-04-24
DD296922A5 (de) 1991-12-19
NZ234296A (en) 1992-11-25
ATE118551T1 (de) 1995-03-15
FI903314A0 (fi) 1990-06-29
PT94527A (pt) 1991-02-08
JPH03117496A (ja) 1991-05-20
DE69016851D1 (de) 1995-03-23

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Legal Events

Date Code Title Description
8364 No opposition during term of opposition
8339 Ceased/non-payment of the annual fee