SK283028B6 - Spôsob prípravy trans-hydroxysulfónu - Google Patents

Spôsob prípravy trans-hydroxysulfónu Download PDF

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Publication number
SK283028B6
SK283028B6 SK315-97A SK31597A SK283028B6 SK 283028 B6 SK283028 B6 SK 283028B6 SK 31597 A SK31597 A SK 31597A SK 283028 B6 SK283028 B6 SK 283028B6
Authority
SK
Slovakia
Prior art keywords
carbon atoms
atcc
added
hydroxysulfone
trans
Prior art date
Application number
SK315-97A
Other languages
English (en)
Slovak (sk)
Other versions
SK31597A3 (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 SK31597A3 publication Critical patent/SK31597A3/sk
Publication of SK283028B6 publication Critical patent/SK283028B6/sk

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)
SK315-97A 1994-09-13 1995-09-08 Spôsob prípravy trans-hydroxysulfónu SK283028B6 (sk)

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 (2)

Publication Number Publication Date
SK31597A3 SK31597A3 (en) 1997-10-08
SK283028B6 true SK283028B6 (sk) 2003-02-04

Family

ID=23179375

Family Applications (1)

Application Number Title Priority Date Filing Date
SK315-97A SK283028B6 (sk) 1994-09-13 1995-09-08 Spôsob prípravy trans-hydroxysulfónu

Country Status (11)

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

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.
WO1996020189A1 (fr) * 1994-12-28 1996-07-04 Kanegafuchi Kagaku Kogyo Kabushiki Kaisha Procede de production d'un derive d'acide carboxylique
ES2155539T3 (es) * 1994-12-28 2001-05-16 Kanegafuchi Chemical Ind Procedimiento para producir un 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
WO2006074230A2 (en) * 2005-01-06 2006-07-13 Teva Gyógyszergyár Zártkörüen Müködö Részvénytársaság Method of making dorzolamide hydrochloride
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
JP2010526127A (ja) * 2007-05-07 2010-07-29 シプラ・リミテッド ドルゾラミドの製造方法
US8927740B2 (en) 2011-03-10 2015-01-06 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
US4968814A (en) * 1990-04-18 1990-11-06 Merck & Co., Inc. (S)-Alkyl 3-(thien-2-ylthio)butyrate and analogs and synthesis thereof
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
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
TW384310B (en) 2000-03-11
FI971035A (fi) 1997-03-12
FI971035A0 (fi) 1997-03-12
AU3464195A (en) 1996-03-29
UA42024C2 (uk) 2001-10-15
WO1996008577A1 (en) 1996-03-21
US5474919A (en) 1995-12-12
BR9508921A (pt) 1997-09-30
CZ289030B6 (cs) 2001-10-17
CZ77497A3 (en) 1997-07-16
SK31597A3 (en) 1997-10-08
RU2134296C1 (ru) 1999-08-10
CN1162980A (zh) 1997-10-22
CN1057796C (zh) 2000-10-25

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