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FI971035L - Biokonversioprosessi trans-hydroksisulfonin syntetisoimiseksi - Google Patents

Biokonversioprosessi trans-hydroksisulfonin syntetisoimiseksi Download PDF

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Publication number
FI971035L
FI971035L FI971035A FI971035A FI971035L FI 971035 L FI971035 L FI 971035L FI 971035 A FI971035 A FI 971035A FI 971035 A FI971035 A FI 971035A FI 971035 L FI971035 L FI 971035L
Authority
FI
Finland
Prior art keywords
hydroxysulfone
bioconversion process
synthesize trans
synthesize
trans
Prior art date
Application number
FI971035A
Other languages
English (en)
Finnish (fi)
Swedish (sv)
Other versions
FI971035A0 (fi
FI971035A7 (fi
Inventor
Michel M Chartrain
Lorraine G Katz
Steven A King
Original Assignee
Merck & Co Inc
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 Merck & Co Inc filed Critical Merck & Co Inc
Publication of FI971035L publication Critical patent/FI971035L/fi
Publication of FI971035A0 publication Critical patent/FI971035A0/fi
Publication of FI971035A7 publication Critical patent/FI971035A7/fi

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
    • C12P17/18Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms containing at least two hetero rings condensed among themselves or condensed with a common carbocyclic ring system, e.g. rifamycin
    • C12P17/185Heterocyclic compounds containing sulfur atoms as ring hetero atoms in the condensed system
    • 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

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)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
FI971035A 1994-09-13 1995-09-08 Biokonversioprosessi trans-hydroksisulfonin syntetisoimiseksi FI971035A7 (fi)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US08/305,110 US5474919A (en) 1994-09-13 1994-09-13 Bioconversion process for the synthesis of transhydroxy sulfone by Rhodotorula rubra or Rhodotorula piliminae
PCT/US1995/011243 WO1996008577A1 (en) 1994-09-13 1995-09-08 Bioconversion process for the synthesis of trans-hydroxy sulfone

Publications (3)

Publication Number Publication Date
FI971035L true FI971035L (fi) 1997-03-12
FI971035A0 FI971035A0 (fi) 1997-03-12
FI971035A7 FI971035A7 (fi) 1997-03-12

Family

ID=23179375

Family Applications (1)

Application Number Title Priority Date Filing Date
FI971035A FI971035A7 (fi) 1994-09-13 1995-09-08 Biokonversioprosessi trans-hydroksisulfonin syntetisoimiseksi

Country Status (11)

Country Link
US (1) US5474919A (ru)
CN (1) CN1057796C (ru)
AU (1) AU3464195A (ru)
BR (1) BR9508921A (ru)
CZ (1) CZ289030B6 (ru)
FI (1) FI971035A7 (ru)
RU (1) RU2134296C1 (ru)
SK (1) SK283028B6 (ru)
TW (1) TW384310B (ru)
UA (1) UA42024C2 (ru)
WO (1) WO1996008577A1 (ru)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5580764A (en) * 1992-08-28 1996-12-03 Zeneca Limited Process for microbial reduction producing 4(S)-hydroxy-6(S)methyl-thienopyran derivatives
PT748803E (pt) * 1994-12-28 2001-07-31 Kanegafuchi Chemical Ind Processo para a preparacao de um derivado de acido carboxilico
JP3777408B2 (ja) * 1994-12-28 2006-05-24 株式会社カネカ カルボン酸誘導体の製造法
US5900368A (en) * 1996-09-17 1999-05-04 Merck & Co., Inc. Process for bioreduction of bisaryl ketone to bisaryl alcohol
ES2177415B1 (es) * 2000-09-04 2004-10-16 Ragactives, S.L. Procedimiento para la obtencion de 4-alquilamino-5, 6-dihidro-4h-tieno-(2,3b)-tiopiran-2-sulfonamida-7-dioxidos, e intermedios.
US20050059583A1 (en) 2003-09-15 2005-03-17 Allergan, Inc. Methods of providing therapeutic effects using cyclosporin components
EP1753769A2 (en) * 2005-01-06 2007-02-21 TEVA Gyógyszergyár Zártkörüen Müködö Részvénytársaság Method of making dorzolamide hydrochloride
US20060173068A1 (en) * 2005-01-18 2006-08-03 Judith Aronhime Amorphous and crystalline forms of dorzolamide hydrochloride and processes of making same
WO2008135770A2 (en) * 2007-05-07 2008-11-13 Cipla Limited Process for preparing dorzolam ide
WO2012120086A1 (en) 2011-03-10 2012-09-13 Zach System S.P.A. Asymmetric reduction process

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4797413A (en) * 1986-05-14 1989-01-10 Merck & Co., Inc. Thieno thiopyran sulfonamide derivatives, pharmaceutical compositions and use
US5371014A (en) * 1988-02-12 1994-12-06 Daicel Chemical Industries, Ltd. Process for the production of optically active 2-hydroxy acid esters using microbes to reduce the 2-oxo precursor
US4968815A (en) * 1990-04-16 1990-11-06 Merck & Co., Inc. Synthesis of (S)-3-(thien-2-ylthio)butyric acid analogs
US5157129A (en) * 1990-04-18 1992-10-20 Merck & Co., Inc. Enantiospecific synthesis of s-(+)-5,6-dihydro-4-(r-amino)-4h-thieno(2,3-b)thiopyran-2-sulfonamide-7,7-dioxide
US4968814A (en) * 1990-04-18 1990-11-06 Merck & Co., Inc. (S)-Alkyl 3-(thien-2-ylthio)butyrate and analogs and synthesis thereof
US5091409A (en) * 1990-05-17 1992-02-25 Merck & Co., Inc. 4-alkylamino-6-(C3-5 -hydrocarbyl)thieno[2,3-B]thiopyran-2-sulfonamide-7,7-dioxides
US5356812A (en) * 1990-08-10 1994-10-18 Daicel Chemical Industries, Ltd. Processes for production of optically active 3-phenyl-1,3-propanediol by asymmetric assimilation
US5352579A (en) * 1991-06-28 1994-10-04 Gen Probe, Inc. Nucleic acid probes to histoplasma capsulatum
US5580764A (en) * 1992-08-28 1996-12-03 Zeneca Limited Process for microbial reduction producing 4(S)-hydroxy-6(S)methyl-thienopyran derivatives
JP3279671B2 (ja) * 1992-09-28 2002-04-30 鐘淵化学工業株式会社 チエノチオピラン誘導体の製造方法

Also Published As

Publication number Publication date
WO1996008577A1 (en) 1996-03-21
TW384310B (en) 2000-03-11
UA42024C2 (ru) 2001-10-15
CZ77497A3 (en) 1997-07-16
AU3464195A (en) 1996-03-29
RU2134296C1 (ru) 1999-08-10
SK31597A3 (en) 1997-10-08
BR9508921A (pt) 1997-09-30
CZ289030B6 (cs) 2001-10-17
FI971035A0 (fi) 1997-03-12
CN1057796C (zh) 2000-10-25
CN1162980A (zh) 1997-10-22
SK283028B6 (sk) 2003-02-04
FI971035A7 (fi) 1997-03-12
US5474919A (en) 1995-12-12

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