KR890002409A - 케톤의 환원방법 - Google Patents
케톤의 환원방법 Download PDFInfo
- Publication number
- KR890002409A KR890002409A KR1019880009015A KR880009015A KR890002409A KR 890002409 A KR890002409 A KR 890002409A KR 1019880009015 A KR1019880009015 A KR 1019880009015A KR 880009015 A KR880009015 A KR 880009015A KR 890002409 A KR890002409 A KR 890002409A
- Authority
- KR
- South Korea
- Prior art keywords
- carbon atoms
- hal
- alkyl
- het
- iii
- Prior art date
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- 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
- C12P7/24—Preparation of oxygen-containing organic compounds containing a carbonyl group
- C12P7/26—Ketones
-
- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/001—Amines; Imines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C227/00—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C227/14—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof
- C07C227/16—Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof by reactions not involving the amino or carboxyl groups
-
- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/002—Nitriles (-CN)
-
- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/005—Amino acids other than alpha- or beta amino acids, e.g. gamma amino acids
-
- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/008—Preparation of nitrogen-containing organic compounds containing a N-O bond, e.g. nitro (-NO2), nitroso (-NO)
-
- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/02—Amides, e.g. chloramphenicol or polyamides; Imides or polyimides; Urethanes, i.e. compounds comprising N-C=O structural element or polyurethanes
-
- 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
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/04—Alpha- or beta- amino acids
-
- 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
-
- 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
- C12P41/002—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by oxidation/reduction reactions
-
- 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
- C12P7/42—Hydroxy-carboxylic acids
-
- 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
- C12P7/62—Carboxylic acid esters
-
- 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
- Y10S435/93—Hansenula
-
- 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
- Y10S435/94—Saccharomyces
- Y10S435/942—Saccharomyces cerevisiae
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Genetics & Genomics (AREA)
- Analytical Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (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)
- Peptides Or Proteins (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (2)
- 미생물에 의해 2급알콜을 생성시키기 위해 케토 화합물의 호변 선택적 환원방법에 있어서, 다음 일반식(Ⅰ)의 화합물을 출발화합물로서 사용함을 특징으로 하는 호변 선택적 환원방법R3NH-CHR1-CO-CH2-COOR2(Ⅰ)상기식에서 R1은 A, Ar, Ar-알킬, HeT, HeT-알킬, 비치환 또는 A, AO 및/또는 Hal로 일치환 또는 다치환 된 탄화수소 3 내지 7의 시클로알킬, 탄소수 4 내지 11의 시클로알킬알킬, 탄소수 7 내지 14의 비시클로알킬 또는 탄소수 8 내지 18의 비시클로알킬알킬이고, R2는 H 또는 탄소수 1 내지 5의 알킬이고, R3는 H, 벤질, 트리페틸메틸, 벤질옥시카보닐, 3급-부틸옥시카보닐 또는 9-플루오레닐메톡시카보닐이고, Ar은 비치환 또는 A, AO, Hal, CF3, HO, 탄소수 1 내지 8의 히드록시알킬, Het는 벤젠링과 융합할 수 있는 1 내지 4의 N, O 및/또는 S원자를 갖고/갖거나, A, AO, Hal, CF3, HO, O2N, 카보닐산소, H2N,HAN, A2N, AS, ASO, ASO2,AOOC, CN, H|uNCO, HOOC, HNSO, ASONH, Ar, Ar懦케닐, 각기 탄소수 1 내지 8을 갖는 히드록시알킬 및/또는 아미노알킬로 일치환 또는 다치환된, 포화 또는 불포화 5-또는 6원 헤테로시클릭래디칼이고/이거나, N 및/또는 S 헤테로원자는 산화될 수도 있고, Hal은 F, Cl, Br 또는 I이고, Ac는 A-CO-, Ar-CO- 또는 A-NH-CO-이고, A는 탄소수 1 내지 8의 알킬이다.
- 다음 구조성분(Ⅲ)을 함유하는 레닌 억제제를 합성하는데 있어서의 다음 일반식(Ⅲ)의 화합물의 용도.R3NH-CHR1-CHOH-CH2-COOR2(Ⅱ) -NH-CH-CHOH-CH2-CO- (Ⅲ)상기 식에서 R1내지 R3는 제1항에서 정의한 바와 같다.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19873724197 DE3724197A1 (de) | 1987-07-22 | 1987-07-22 | Verfahren zur reduktion von ketonen |
DEP3724197.4 | 1987-07-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
KR890002409A true KR890002409A (ko) | 1989-04-10 |
Family
ID=6332081
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019880009015A KR890002409A (ko) | 1987-07-22 | 1988-07-19 | 케톤의 환원방법 |
Country Status (14)
Country | Link |
---|---|
US (1) | US5026642A (ko) |
EP (1) | EP0300287B1 (ko) |
JP (1) | JPS6455187A (ko) |
KR (1) | KR890002409A (ko) |
AR (1) | AR240064A1 (ko) |
AT (1) | ATE84317T1 (ko) |
AU (1) | AU628289B2 (ko) |
DD (1) | DD272475A5 (ko) |
DE (2) | DE3724197A1 (ko) |
DK (1) | DK409388A (ko) |
ES (1) | ES2043738T3 (ko) |
FI (1) | FI883457A (ko) |
HU (1) | HU203905B (ko) |
ZA (1) | ZA885365B (ko) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100411685B1 (ko) * | 2001-10-31 | 2003-12-18 | (주)그린앤크린 | 대두지방산과 레시틴을 이용한 활성 수용성 천연세제조성물 및 그 제조방법 |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5232853A (en) * | 1989-12-28 | 1993-08-03 | Takeda Chemical Industries, Ltd. | Method for producing (2r,3s)-3-hydroxy-2-methylbutyrate by microbial reduction |
US5215919A (en) * | 1991-02-25 | 1993-06-01 | Takeda Chemical Industries, Ltd. | Process for producing optically active 2-hydroxycycloalkanecarboxylic acid esters using microbially derived reductase |
WO1993007289A1 (en) * | 1991-10-04 | 1993-04-15 | Schering Corporation | ENZYMATIC SYNTHESIS OF CHIRAL α-HYDROXYKETONES AND DERIVATIVES |
DE4209022B4 (de) * | 1992-03-20 | 2006-01-19 | Forschungszentrum Jülich GmbH | Verfahren zur enzymatischen Herstellung von sekundären (S)-Alkoholen |
US5324662A (en) * | 1992-05-15 | 1994-06-28 | E. R. Squibb & Sons, Inc. | Stereoselective microbial or enzymatic reduction of 3,5-dioxo esters to 3-hydroxy-5-oxo, 3-oxo-5-hydroxy, and 3,5-dihydroxy esters |
CA2103932A1 (en) * | 1992-11-05 | 1994-05-06 | Ramesh N. Patel | Stereoselective reduction of ketones |
GB9512837D0 (en) * | 1995-06-23 | 1995-08-23 | Zeneca Ltd | reduction of ketone groups |
JP2002513573A (ja) | 1998-05-07 | 2002-05-14 | ドゥーサン コーポレーション | ピヒア・シフェリにおける遺伝子発現のためのプラスミド及びこれを用いた形質転換方法 |
US10784121B2 (en) | 2016-08-15 | 2020-09-22 | Xilinx, Inc. | Standalone interface for stacked silicon interconnect (SSI) technology integration |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4478826A (en) * | 1981-10-08 | 1984-10-23 | Merck & Co., Inc. | Renin inhibitory peptides |
CA1258748A (en) * | 1981-10-08 | 1989-08-22 | Daniel F. Veber | Renin inhibitory peptides |
EP0104041B1 (en) * | 1982-09-15 | 1988-07-27 | Aktiebolaget Hässle | Enzyme inhibitors |
US4650661A (en) * | 1982-09-15 | 1987-03-17 | Aktiebolaget Hassle | Enzyme inhibitors |
US4477440A (en) * | 1983-09-14 | 1984-10-16 | Merck & Co., Inc. | Renin inhibitors containing an n-terminal disulfide cycle |
KR870005013A (ko) * | 1985-11-29 | 1987-06-04 | 가와무라 요시부미 | 레닌-억제 올리고펩티드, 그의 제조방법 및 용도 |
-
1987
- 1987-07-22 DE DE19873724197 patent/DE3724197A1/de not_active Withdrawn
-
1988
- 1988-06-21 AU AU18232/88A patent/AU628289B2/en not_active Ceased
- 1988-07-08 DE DE8888110912T patent/DE3877275D1/de not_active Expired - Fee Related
- 1988-07-08 EP EP88110912A patent/EP0300287B1/de not_active Expired - Lifetime
- 1988-07-08 ES ES88110912T patent/ES2043738T3/es not_active Expired - Lifetime
- 1988-07-08 AT AT88110912T patent/ATE84317T1/de not_active IP Right Cessation
- 1988-07-19 KR KR1019880009015A patent/KR890002409A/ko not_active Application Discontinuation
- 1988-07-20 AR AR311459A patent/AR240064A1/es active
- 1988-07-20 DD DD88318118A patent/DD272475A5/de not_active IP Right Cessation
- 1988-07-21 FI FI883457A patent/FI883457A/fi not_active IP Right Cessation
- 1988-07-21 DK DK409388A patent/DK409388A/da not_active Application Discontinuation
- 1988-07-21 HU HU883801A patent/HU203905B/hu not_active IP Right Cessation
- 1988-07-21 JP JP63180461A patent/JPS6455187A/ja active Pending
- 1988-07-22 US US07/223,051 patent/US5026642A/en not_active Expired - Fee Related
- 1988-07-22 ZA ZA885365A patent/ZA885365B/xx unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100411685B1 (ko) * | 2001-10-31 | 2003-12-18 | (주)그린앤크린 | 대두지방산과 레시틴을 이용한 활성 수용성 천연세제조성물 및 그 제조방법 |
Also Published As
Publication number | Publication date |
---|---|
DK409388D0 (da) | 1988-07-21 |
ZA885365B (en) | 1989-03-29 |
DE3724197A1 (de) | 1989-02-02 |
FI883457A (fi) | 1989-01-23 |
JPS6455187A (en) | 1989-03-02 |
EP0300287A2 (de) | 1989-01-25 |
AR240064A1 (es) | 1990-01-31 |
ES2043738T3 (es) | 1994-01-01 |
FI883457A0 (fi) | 1988-07-21 |
EP0300287B1 (de) | 1993-01-07 |
HU203905B (en) | 1991-10-28 |
HUT47642A (en) | 1989-03-28 |
AU1823288A (en) | 1989-01-27 |
DK409388A (da) | 1989-01-23 |
DD272475A5 (de) | 1989-10-11 |
EP0300287A3 (en) | 1989-05-03 |
AU628289B2 (en) | 1992-09-17 |
ATE84317T1 (de) | 1993-01-15 |
US5026642A (en) | 1991-06-25 |
DE3877275D1 (de) | 1993-02-18 |
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