IT1201408B - Processo per la preparazione biotecnologica di acidi alfa-arilalcanoici otticamente attivi - Google Patents

Processo per la preparazione biotecnologica di acidi alfa-arilalcanoici otticamente attivi

Info

Publication number: IT1201408B
Authority: IT; Italy
Prior art keywords: acids; arilalcanoic; optically active; alkyl; aryl
Prior art date: 1985-03-22

Application number

IT20036/85A

Other languages

English (en)

Other versions

IT8520036A0 (it

Inventor

Pietro Cesti

Paolo Piccardi

Original Assignee

Montedison Spa

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.)

1985-03-22

Filing date

1985-03-22

Publication date

1989-02-02

1985-03-22 Application filed by Montedison Spa filed Critical Montedison Spa

1985-03-22 Publication of IT8520036A0 publication Critical patent/IT8520036A0/it

1985-03-22 Priority to IT20036/85A priority Critical patent/IT1201408B/it

1986-03-17 Priority to EP86400558A priority patent/EP0195717B1/en

1986-03-17 Priority to AT86400558T priority patent/ATE68210T1/de

1986-03-17 Priority to DE8686400558T priority patent/DE3681810D1/de

1986-03-17 Priority to KR1019860001932A priority patent/KR860007381A/ko

1986-03-18 Priority to US06/840,856 priority patent/US4762793A/en

1986-03-20 Priority to JP61061067A priority patent/JPS61239899A/ja

1986-03-21 Priority to ES553215A priority patent/ES8705842A1/es

1986-03-21 Priority to HU861202A priority patent/HU197943B/hu

1989-02-02 Application granted granted Critical

1989-02-02 Publication of IT1201408B publication Critical patent/IT1201408B/it

Links

239000002253 acid Substances 0.000 title abstract 3
150000007513 acids Chemical class 0.000 title abstract 2
150000002148 esters Chemical class 0.000 abstract 3
125000003118 aryl group Chemical group 0.000 abstract 2
125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
125000004399 C1-C4 alkenyl group Chemical group 0.000 abstract 1
108090000371 Esterases Proteins 0.000 abstract 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
125000000217 alkyl group Chemical group 0.000 abstract 1
125000004432 carbon atom Chemical group C* 0.000 abstract 1
229910052736 halogen Inorganic materials 0.000 abstract 1
150000002367 halogens Chemical class 0.000 abstract 1
125000000623 heterocyclic group Chemical group 0.000 abstract 1
229910052739 hydrogen Inorganic materials 0.000 abstract 1
239000001257 hydrogen Substances 0.000 abstract 1
230000003301 hydrolyzing effect Effects 0.000 abstract 1
244000005700 microbiome Species 0.000 abstract 1
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 abstract 1

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
- C12P5/00—Preparation of hydrocarbons or halogenated hydrocarbons
- 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
- C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
- C12P41/003—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
- C12P41/005—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions by esterification of carboxylic acid groups in the enantiomers or the inverse reaction
- 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
- C12P17/10—Nitrogen as only ring hetero atom
- 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
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/40—Preparation of oxygen-containing organic compounds containing a carboxyl group including Peroxycarboxylic acids
- 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
- Y10S435/921—Candida

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Life Sciences & Earth Sciences (AREA)
Zoology (AREA)
Wood Science & Technology (AREA)
Health & Medical Sciences (AREA)
General Engineering & Computer Science (AREA)
General Chemical & Material Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Biotechnology (AREA)
Biochemistry (AREA)
Bioinformatics & Cheminformatics (AREA)
Microbiology (AREA)
General Health & Medical Sciences (AREA)
Genetics & Genomics (AREA)
Analytical Chemistry (AREA)
Preparation Of Compounds By Using Micro-Organisms (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

IT20036/85A 1985-03-22 1985-03-22 Processo per la preparazione biotecnologica di acidi alfa-arilalcanoici otticamente attivi IT1201408B (it)

Priority Applications (9)

Application Number	Priority Date	Filing Date	Title
IT20036/85A IT1201408B (it)	1985-03-22	1985-03-22	Processo per la preparazione biotecnologica di acidi alfa-arilalcanoici otticamente attivi
KR1019860001932A KR860007381A (ko)	1985-03-22	1986-03-17	광학활성 α-아릴알칸산의 생물공학적 제조방법
AT86400558T ATE68210T1 (de)	1985-03-22	1986-03-17	Verfahren zur biotechnologischen herstellung von optisch aktiven alpha-arylalkansaeuren.
DE8686400558T DE3681810D1 (de)	1985-03-22	1986-03-17	Verfahren zur biotechnologischen herstellung von optisch aktiven alpha-arylalkansaeuren.
EP86400558A EP0195717B1 (en)	1985-03-22	1986-03-17	Process for the biotechnological preparation of optically active alpha-arylalkanoic acids
US06/840,856 US4762793A (en)	1985-03-22	1986-03-18	Process for the biotechnological preparation of optically active alpha-arylalkanoic acids
JP61061067A JPS61239899A (ja)	1985-03-22	1986-03-20	光学活性アルフア‐アリールアルカン酸の生物工学的製造方法
ES553215A ES8705842A1 (es)	1985-03-22	1986-03-21	Procedimiento para la preparacion biotecnologica de acidos alfa-arilalcanoicos activos opticamente
HU861202A HU197943B (en)	1985-03-22	1986-03-21	Process for producing optically active alpha-arylalkane acids in biotechnological way

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
IT20036/85A IT1201408B (it)	1985-03-22	1985-03-22	Processo per la preparazione biotecnologica di acidi alfa-arilalcanoici otticamente attivi

Publications (2)

Publication Number	Publication Date
IT8520036A0 IT8520036A0 (it)	1985-03-22
IT1201408B true IT1201408B (it)	1989-02-02

Family

ID=11163308

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IT20036/85A IT1201408B (it)	1985-03-22	1985-03-22	Processo per la preparazione biotecnologica di acidi alfa-arilalcanoici otticamente attivi

Country Status (9)

Country	Link
US (1)	US4762793A (it)
EP (1)	EP0195717B1 (it)
JP (1)	JPS61239899A (it)
KR (1)	KR860007381A (it)
AT (1)	ATE68210T1 (it)
DE (1)	DE3681810D1 (it)
ES (1)	ES8705842A1 (it)
HU (1)	HU197943B (it)
IT (1)	IT1201408B (it)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB8514489D0 (en) *	1985-06-07	1985-07-10	Shell Int Research	Producing 2-arylpropionic acids
US5322791A (en) *	1985-12-20	1994-06-21	Wisconsin Alumni Research Foundation	Process for preparing (S)-α-methylarylacetic acids
US4897357A (en) *	1985-12-31	1990-01-30	Ethyl Corporation	(S) α-cyano-3-phenoxy-benzyl acetate
GB8600245D0 (en) *	1986-01-07	1986-02-12	Shell Int Research	Preparation of 2-arylpropionic acids
GB8705601D0 (en) *	1987-03-10	1987-04-15	Erba Farmitalia	Oxo-isoindolinyl derivatives
GB8715476D0 (en) *	1987-07-01	1987-08-05	Shell Int Research	Preparation of ibuprofen
GB8715574D0 (en) *	1987-07-02	1987-08-12	Shell Int Research	2-aryloxypropionic acids
US5229280A (en) *	1988-02-25	1993-07-20	Istituto Guido Donegani S.P.A.	Process for the continuous biotechnological preparation of optical isomer s(+) of 2-(6-methoxy-2-naphthyl) propionic acid
US6054566A (en)	1988-02-26	2000-04-25	Biosource Technologies, Inc.	Recombinant animal viral nucleic acids
US6284492B1 (en)	1988-02-26	2001-09-04	Large Scale Biology Corporation	Recombinant animal viral nucleic acids
US5316931A (en) *	1988-02-26	1994-05-31	Biosource Genetics Corp.	Plant viral vectors having heterologous subgenomic promoters for systemic expression of foreign genes
JPH01228488A (ja) *	1988-03-09	1989-09-12	Fuji Yakuhin Kogyo Kk	パントテン酸またはその塩の製造法
US5057427A (en) *	1988-04-07	1991-10-15	Sepracor, Inc.	Method for resolution of stereoisomers
AU643210B2 (en) *	1989-05-16	1993-11-11	Medice Chem.-Pharm. Fabrik Putter Gmbh & Co. Kg	Process for preparing optically active 2-aryl-alkanoic acids, in particular 2-ayrl-propionic acids
US5266723A (en) *	1989-05-16	1993-11-30	Medice, Ltd., Chem.-Pharm. Fabrik Putter Gmbh & Co. Kg	Process for the preparation of optically active 2-aryl-alkanoic acids, especially 2-aryl-propionic acids
DE3919029A1 (de) *	1989-06-10	1990-12-13	Hoechst Ag	Verfahren zur enzymatischen spaltung von 2-arylpropionsaeure-vinylester
US4921798A (en) *	1989-09-25	1990-05-01	Eastman Kodak Company	Synthesis of (aryl or arylalkyl)-3-hydroxy propionic acids and aryl alkanediols having high optical purity
DE59205454D1 (de) *	1991-08-22	1996-04-04	Lonza Ag	Verfahren zur Herstellung von optisch aktiven 4-Amino-3-hydroxycarbonsäuren
EP0939135A1 (en) *	1992-12-21	1999-09-01	Duphar International Research B.V	Substantially pure hetero-bicyclic alcohol enantiomers
US5912164A (en) *	1993-03-03	1999-06-15	Laboratorios Menarini S.A.	Stereoselective hydrolysis of chiral carboxylic acid esters using esterase from ophiostoma or ceratocystis
GB9304351D0 (en) *	1993-03-03	1993-04-21	Chiros Ltd	Arylalkanoic acid resolution and microorganisms for use therein
US5457051A (en) *	1993-03-09	1995-10-10	Sepracor, Inc.	Enantioselective hydrolysis of ketoprofen esters by beauveria bassiana and enzymes derived therefrom
US5434302A (en) *	1994-02-18	1995-07-18	Paradies; H. Henrich	Method for the preparation of optically active 2-aryl alkyl aldehydes and formation of 2-aryl-alkanoic acids therefrom
AU7324696A (en) *	1995-11-17	1997-06-11	Aeci Limited	Synthesis of propionic acid derivatives
US6242243B1 (en) *	1998-03-30	2001-06-05	Council Of Scientific & Industrial Research	Trichosporon sp RRLY-15 (DSM 11829) and its use to prepare S(+)-6-methoxy-methyl-2-naphthalene acetic acid
US6201151B1 (en) *	1998-12-17	2001-03-13	National Science Council Of Republic Of China	Processes for preparing optically active (S)-α-aryl propionic acid or ester therof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA1215924A (en) *	1983-07-27	1986-12-30	David W. Bewick	Process for producing optically active aryloxypropionic acids and derivatives thereof useful as herbicides

1985
- 1985-03-22 IT IT20036/85A patent/IT1201408B/it active
1986
- 1986-03-17 KR KR1019860001932A patent/KR860007381A/ko not_active Ceased
- 1986-03-17 EP EP86400558A patent/EP0195717B1/en not_active Expired - Lifetime
- 1986-03-17 DE DE8686400558T patent/DE3681810D1/de not_active Expired - Lifetime
- 1986-03-17 AT AT86400558T patent/ATE68210T1/de not_active IP Right Cessation
- 1986-03-18 US US06/840,856 patent/US4762793A/en not_active Expired - Fee Related
- 1986-03-20 JP JP61061067A patent/JPS61239899A/ja active Pending
- 1986-03-21 HU HU861202A patent/HU197943B/hu not_active IP Right Cessation
- 1986-03-21 ES ES553215A patent/ES8705842A1/es not_active Expired

Also Published As

Publication number	Publication date
ATE68210T1 (de)	1991-10-15
EP0195717A3 (en)	1989-02-22
IT8520036A0 (it)	1985-03-22
ES553215A0 (es)	1987-05-16
US4762793A (en)	1988-08-09
HU197943B (en)	1989-06-28
DE3681810D1 (de)	1991-11-14
EP0195717A2 (en)	1986-09-24
ES8705842A1 (es)	1987-05-16
KR860007381A (ko)	1986-10-10
HUT41069A (en)	1987-03-30
EP0195717B1 (en)	1991-10-09
JPS61239899A (ja)	1986-10-25

Publication	Publication Date	Title
IT1201408B (it)	1989-02-02	Processo per la preparazione biotecnologica di acidi alfa-arilalcanoici otticamente attivi
ES2043106T3 (es)	1993-12-16	Procedimiento para preparar s-metoprolol y sus productos intermedios.
DE3783901D1 (de)	1993-03-11	Verfahren zur enzymatischen trennung der optischen isomere von racemischen oxazolidinon-derivaten.
DE68920648D1 (de)	1995-03-02	Verfahren zur Herstellung von O2,2'-anhydro-1-(beta-D-arabinofuranosyl)Thymin.
Hamaguchi et al.	1985	Enzymatic resolution of 2-oxazolidinone esters
IT1226903B (it)	1991-02-21	Processo per la sintesi di aminoacidi otticamente attivi
ATE74380T1 (de)	1992-04-15	Verfahren zur herstellung von 2-arylpropionsaeure.
DE3780616D1 (de)	1992-08-27	Verfahren zur herstellung eines 2-alkyl- oder 2-phenyl-1,4,5,6-tetrahydropyrimidins und verfahren zur herstellung von 2-alkyl- oder 2-phenyl-pyrimidinen.
ATE18208T1 (de)	1986-03-15	N-(4-hydroxyphenyl)essigsaeureamid-estern aus 5benzoyl-1-methylpyrrol-2-essigsaeure.
ATE38980T1 (de)	1988-12-15	Verfahren zur herstellung von l-carnitin.
ATE77412T1 (de)	1992-07-15	Verfahren zur enzymatischen auftrennung von racemischen 2-amino-1-alkanolen.