BR9508921A - Processo de bioconversão para a sintese de trans-hidr xi sulfona - Google Patents

Processo de bioconversão para a sintese de trans-hidr xi sulfona

Info

Publication number
BR9508921A
BR9508921A BR9508921A BR9508921A BR9508921A BR 9508921 A BR9508921 A BR 9508921A BR 9508921 A BR9508921 A BR 9508921A BR 9508921 A BR9508921 A BR 9508921A BR 9508921 A BR9508921 A BR 9508921A
Authority
BR
Brazil
Prior art keywords
hydroxysulfone
trans
synthesis
bioconversion process
bioconversion
Prior art date
Application number
BR9508921A
Other languages
English (en)
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 BR9508921A publication Critical patent/BR9508921A/pt

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
    • C12P17/00—Preparation of heterocyclic carbon compounds with only O, N, S, Se or Te as ring hetero atoms
    • C12P17/18—Preparation 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
    • C12P17/185—Heterocyclic compounds containing sulfur atoms as ring hetero atoms in the condensed system
    • Y—GENERAL 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
    • Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S435/00—Chemistry: molecular biology and microbiology
    • Y10S435/8215—Microorganisms
    • Y10S435/911—Microorganisms 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)
BR9508921A 1994-09-13 1995-09-08 Processo de bioconversão para a sintese de trans-hidr xi sulfona BR9508921A (pt)

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 (1)

Publication Number Publication Date
BR9508921A true BR9508921A (pt) 1997-09-30

Family

ID=23179375

Family Applications (1)

Application Number Title Priority Date Filing Date
BR9508921A BR9508921A (pt) 1994-09-13 1995-09-08 Processo de bioconversão para a sintese de trans-hidr xi sulfona

Country Status (11)

Country Link
US (1) US5474919A (pt)
CN (1) CN1057796C (pt)
AU (1) AU3464195A (pt)
BR (1) BR9508921A (pt)
CZ (1) CZ289030B6 (pt)
FI (1) FI971035A0 (pt)
RU (1) RU2134296C1 (pt)
SK (1) SK283028B6 (pt)
TW (1) TW384310B (pt)
UA (1) UA42024C2 (pt)
WO (1) WO1996008577A1 (pt)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2093980T3 (es) * 1992-08-28 1997-01-01 Zeneca Ltd Proceso de reduccion asimetrica, enzimatica, para producir derivados de 4h-tieno(2,3-6)tiopirano.
EP0748804B1 (en) * 1994-12-28 2001-03-14 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha Process for producing carboxylic acid derivative
PT748803E (pt) * 1994-12-28 2001-07-31 Kanegafuchi Chemical Ind Processo para a preparacao de um derivado de acido carboxilico
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
CN101098874A (zh) * 2005-01-06 2008-01-02 特瓦药厂私人有限公司 制备盐酸多佐胺的方法
JP2008526780A (ja) * 2005-01-18 2008-07-24 テバ ジョジセルジャール ザ−トケルエン ムケド レ−スベニュタ−ルシャシャ−グ ドルゾルアミド塩酸塩の非晶質および結晶質の形態およびそれらを製造する方法
EP2152718A2 (en) * 2007-05-07 2010-02-17 Cipla Limited Process for preparing dorzolamide
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
DE69123041T2 (de) * 1990-08-10 1997-04-03 Daicel Chem Herstellungsverfahren für optisch aktiven 3-phenyl-1,3-propandiol
US5352579A (en) * 1991-06-28 1994-10-04 Gen Probe, Inc. Nucleic acid probes to histoplasma capsulatum
ES2093980T3 (es) * 1992-08-28 1997-01-01 Zeneca Ltd Proceso de reduccion asimetrica, enzimatica, para producir derivados de 4h-tieno(2,3-6)tiopirano.
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
CN1162980A (zh) 1997-10-22
WO1996008577A1 (en) 1996-03-21
RU2134296C1 (ru) 1999-08-10
SK31597A3 (en) 1997-10-08
US5474919A (en) 1995-12-12
CZ289030B6 (cs) 2001-10-17
SK283028B6 (sk) 2003-02-04
TW384310B (en) 2000-03-11
CZ77497A3 (en) 1997-07-16
FI971035A (fi) 1997-03-12
UA42024C2 (uk) 2001-10-15
FI971035A0 (fi) 1997-03-12
CN1057796C (zh) 2000-10-25
AU3464195A (en) 1996-03-29

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Legal Events

Date Code Title Description
EG Technical examination (opinion): publication of technical examination (opinion)
FC Decision: refusal