KR900006284A - 이미도-유도 과산화산 - Google Patents
이미도-유도 과산화산 Download PDFInfo
- Publication number
- KR900006284A KR900006284A KR1019890015292A KR890015292A KR900006284A KR 900006284 A KR900006284 A KR 900006284A KR 1019890015292 A KR1019890015292 A KR 1019890015292A KR 890015292 A KR890015292 A KR 890015292A KR 900006284 A KR900006284 A KR 900006284A
- Authority
- KR
- South Korea
- Prior art keywords
- acid
- imido
- essentially
- hexahydrophthalimido
- succinimido
- Prior art date
Links
- 150000002978 peroxides Chemical class 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 10
- 238000000034 method Methods 0.000 claims 9
- SCKXCAADGDQQCS-UHFFFAOYSA-N Performic acid Chemical compound OOC=O SCKXCAADGDQQCS-UHFFFAOYSA-N 0.000 claims 6
- 125000004432 carbon atom Chemical group C* 0.000 claims 6
- 125000000217 alkyl group Chemical group 0.000 claims 5
- 239000000758 substrate Substances 0.000 claims 5
- -1 3,4,5,6-tetrahydrophthalimido Chemical group 0.000 claims 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 4
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 3
- 238000004519 manufacturing process Methods 0.000 claims 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims 2
- 239000002253 acid Substances 0.000 claims 2
- 150000007513 acids Chemical class 0.000 claims 2
- 125000001931 aliphatic group Chemical group 0.000 claims 2
- GNMJZTJCEDYPIE-UHFFFAOYSA-N 2-(1,3-dioxo-3a,4,5,6,7,7a-hexahydroisoindol-2-yl)propanoic acid Chemical compound C1CCCC2C(=O)N(C(C)C(O)=O)C(=O)C21 GNMJZTJCEDYPIE-UHFFFAOYSA-N 0.000 claims 1
- ZQBWYXZRSMMISZ-UHFFFAOYSA-N 2-(2,5-dioxopyrrolidin-1-yl)acetic acid Chemical compound OC(=O)CN1C(=O)CCC1=O ZQBWYXZRSMMISZ-UHFFFAOYSA-N 0.000 claims 1
- UJSKWPYFGGRAEY-UHFFFAOYSA-N 2-(2,5-dioxopyrrolidin-1-yl)ethaneperoxoic acid Chemical compound OOC(=O)CN1C(=O)CCC1=O UJSKWPYFGGRAEY-UHFFFAOYSA-N 0.000 claims 1
- IJLCTNHKIXADOV-UHFFFAOYSA-N 3-(1,3-dioxo-3a,4,5,6,7,7a-hexahydroisoindol-2-yl)propanoic acid Chemical compound C1CCCC2C(=O)N(CCC(=O)O)C(=O)C21 IJLCTNHKIXADOV-UHFFFAOYSA-N 0.000 claims 1
- DPISPNNORVOBQY-UHFFFAOYSA-N 3-(2,5-dioxopyrrolidin-1-yl)propanoic acid Chemical compound OC(=O)CCN1C(=O)CCC1=O DPISPNNORVOBQY-UHFFFAOYSA-N 0.000 claims 1
- PDTMETFOBGFEEU-UHFFFAOYSA-N 4-(1,3-dioxo-3a,4,5,6,7,7a-hexahydroisoindol-2-yl)butanoic acid Chemical compound C1CCCC2C(=O)N(CCCC(=O)O)C(=O)C21 PDTMETFOBGFEEU-UHFFFAOYSA-N 0.000 claims 1
- NYLWVYIFDBXHBL-UHFFFAOYSA-N 4-(1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)butanoic acid Chemical compound O=C1N(CCCC(=O)O)C(=O)C2=C1CCCC2 NYLWVYIFDBXHBL-UHFFFAOYSA-N 0.000 claims 1
- SIILHQSLHMQZQO-UHFFFAOYSA-N 4-(2,5-dioxopyrrolidin-1-yl)butanoic acid Chemical group OC(=O)CCCN1C(=O)CCC1=O SIILHQSLHMQZQO-UHFFFAOYSA-N 0.000 claims 1
- 102000004190 Enzymes Human genes 0.000 claims 1
- 108090000790 Enzymes Proteins 0.000 claims 1
- YZCKVEUIGOORGS-IGMARMGPSA-N Protium Chemical compound [1H] YZCKVEUIGOORGS-IGMARMGPSA-N 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 239000007844 bleaching agent Substances 0.000 claims 1
- LBAYFEDWGHXMSM-UHFFFAOYSA-N butaneperoxoic acid Chemical compound CCCC(=O)OO LBAYFEDWGHXMSM-UHFFFAOYSA-N 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 150000001735 carboxylic acids Chemical class 0.000 claims 1
- 238000005260 corrosion Methods 0.000 claims 1
- 230000007797 corrosion Effects 0.000 claims 1
- 239000003599 detergent Substances 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 230000036039 immunity Effects 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- 239000003112 inhibitor Substances 0.000 claims 1
- 239000000203 mixture Substances 0.000 claims 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims 1
- 239000011541 reaction mixture Substances 0.000 claims 1
- 239000000344 soap Substances 0.000 claims 1
- 239000008137 solubility enhancer Substances 0.000 claims 1
- 239000003381 stabilizer Substances 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- 239000010457 zeolite Substances 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/32—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D207/325—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with substituted hydrocarbon radicals directly attached to the ring nitrogen atom
- C07D207/327—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D207/36—Oxygen or sulfur atoms
- C07D207/40—2,5-Pyrrolidine-diones
- C07D207/404—2,5-Pyrrolidine-diones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms, e.g. succinimide
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/44—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members
- C07D207/444—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5
- C07D207/448—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5 with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms, e.g. maleimide
- C07D207/452—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5 with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms, e.g. maleimide with hydrocarbon radicals, substituted by hetero atoms, directly attached to the ring nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/44—Iso-indoles; Hydrogenated iso-indoles
- C07D209/48—Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Detergent Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Indole Compounds (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Pyrrole Compounds (AREA)
Abstract
내용 없음
Description
본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음
Claims (19)
- 하기 일반식(I)의 이미도 유도 퍼옥시카르복실산[식중 ; R 및 R1은 서로 동일 또는 상이할 수 있으며, 수소원자, 알킬기를 나타내거나 또는 그것이 결합된 탄소원자와 함께 지방족 고리를 형성하며 ; 이들 모두는 제조조건에 불활성인 기에 의해 임의로 치환될 수 있으며 ; 기호는 단일 또는 올레핀 결합을 의미하며 ; R2는 수소원자, 알킬기, OH기를 나타내고, n은 0 이 아닌 정수이다.]
- 제 1 항에 있어서, 식중, R 및 R1은 서로 동일 또는 상이할 수 있으며, 수소원자 또는 1 내지 12개의 탄소원자를 함유하는 선형 또는 분지형 알킬기를 나타내며 ; R2는 수소원자 또는 1 내지 5개의 탄소원자를 함유하는 선형 또는 분지형 알킬기 또는 OH기를 나타내고 n은 1 내지 10의 정수를 나타내는 일반식(I)의 이미도-유도 퍼옥시카르복실산.
- 제 1 항 또는 제 2 항에 있어서, 식중, R1및 R2는 그것이 결합된 탄소원자와 함께 4 내지 12개의 탄소원자, 바람직하게는 5 내지 6개의 탄소원자를 함유하는 지방족 고리를 형성하는 선형 또는 분지형 알킬기를 나타내는 일반식(I)의 이미도-유도 퍼옥시카르복실산.
- 제 1 항 내지 제 3 항중 어느 한 항에 있어서, 식중, R, R1및 (CHR1)n기는 F,Cl, OH기, NO2, C1~C5알콕시기로 이루어진 군으로부터 선택된 서로 동일 또는 상이할 수 있는 적어도 하나의 치환체에 의해 치환될 수 있는 일반식(I)의 이미도-유도 퍼옥시카르복실산.
- 본질적으로 신규 화합물인 4-숙신이미도-퍼부티르산.
- 본질적으로 신규 화합물인 3-숙신이미도-퍼프로피온산.
- 본질적으로 신규 화합물인 숙신이미도-퍼아세트산.
- 본질적으로 신규 화합물인 4-헥사히드로프탈이미도-퍼부티르산.
- 본질적으로 신규 화합물인 3-헥사히드로프탈이미도-퍼프로피온산.
- 본질적으로 신규 화합물인 2-헥사히드로프탈이미도-3-메틸-퍼부티르산.
- 본질적으로 신규 화합물인 2-헥사히드로프탈이미도-퍼프로피온산.
- 본질적으로 신규 화합물인 4-(3,4,5,6-테트라히드로프탈이미도)퍼부티르산.
- 일반식(I)의 목적하는 퍼옥시카르복실산에 상응하는 이미도-유도 카르복실산으로부터 선택된 기질을 진한 H2SO4및 CH2SO3H로부터 선택된 매질내에서 진한 H2O2와 반응 시킨후, 반응 혼합물로부터 퍼옥시카르복실산(I)을 공지된 방법에 따라 분리시킴을 특징으로 하는 청구범위 제 1 항에서 정의된 일반식(I)의 이미도-유도 퍼옥시카르복실산의 제조방법.
- 제 13항에 있어서, 기질은 4-숙신이미도 부티르산, 3-숙신이미도 프로피온산, 숙신 이미도 아세트산, 4-헥사히드로프탈이미도 부티르산, 3-헥사히드로프탈이미도 프로피온산, 2-헥사히드로프탈이미도-3-메틸-부티르산, 2-헥사히드로프탈이미도 프로피온산, 4-(3,4,5,6-테트라히드로프탈이미도) 부티르산중에서 선택됨을 특징으로 하는 제조방법.
- 제 13항 또는 제 14항에 있어서, 이미도-유도 카르복실산 기질을 약 70 내지 90 중량%범위의 농도를 가진 H2O2와 0 내지 약 15℃의 온도범위에서 진한 H2SO4또는 CH2SO3H내에서 서서히 반응시킴을 특징으로 하는 제조방법.
- 제 13 항 내지 제 15항중 어느 한 항에 있어서, H2SO4또는 CH2SO3H의 양은 기질 1몰당 적어도 3몰, 바람직하게는 약 3 내지 20몰의 범위내임을 특징으로 하는 제조방법.
- 제 13항 내지 제 16항중 어느 한 항에 있어서, 과산화수소를 기질 1몰당 적어도 1.2몰, 바람직하게는 약 1.5 내지 6몰의 범위내로 사용함을 특징으로 하는 제조방법.
- 제 13항 내지 제 17항중 어느 한 항에 있어서, 반응 완료시 존재하는 총 H2O에 대한 H2SO4또는 CH2SO3H의 최종 몰비가 적어도 1.0, 바람직하게는 약 1.2 내지 5 임을 특징으로 하는 제조방법.
- 다른 성분 및/또는 첨가제, 빌더, 계면 활성제, 비누, 제올라이트, 용해도증대제, 부식 방지제, 효소, 형광 표백제, 안정제 및 기타 과산화화합물을 함유하는 세제 배합물에 있어 표백제로서의 일반식(I)의 이미도-유도 퍼옥시카르복실산의 용도.※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
IT8822402A IT1230595B (it) | 1988-10-24 | 1988-10-24 | Perossiacidi immido derivati |
IT22402A/88 | 1988-10-24 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR900006284A true KR900006284A (ko) | 1990-05-07 |
KR0140220B1 KR0140220B1 (ko) | 1998-06-01 |
Family
ID=11195821
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019890015292A KR0140220B1 (ko) | 1988-10-24 | 1989-10-24 | 이미도-유도 과산화산 |
Country Status (10)
Country | Link |
---|---|
US (1) | US5536434A (ko) |
EP (1) | EP0366041B2 (ko) |
JP (1) | JP2915020B2 (ko) |
KR (1) | KR0140220B1 (ko) |
AT (1) | ATE169289T1 (ko) |
AU (1) | AU619607B2 (ko) |
BR (1) | BR8905400A (ko) |
CA (1) | CA2001184A1 (ko) |
DE (1) | DE68928767T3 (ko) |
IT (1) | IT1230595B (ko) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
IT1215739B (it) * | 1988-01-20 | 1990-02-22 | Ausimont Spa | Perossiacidi immido aromatici come agenti sbiancanti. |
EP0484095B1 (en) * | 1990-11-02 | 1996-03-20 | The Clorox Company | Liquid nonaqueous detergent with stable, solublized peracid |
GB9105959D0 (en) * | 1991-03-21 | 1991-05-08 | Unilever Plc | Cationic peroxyacids and bleach compositions comprising said peroxyacids |
US5985815A (en) * | 1993-11-25 | 1999-11-16 | Warwick International Group Limited | Bleach activators |
GB9501737D0 (en) * | 1994-04-25 | 1995-03-22 | Hoffmann La Roche | Hydroxamic acid derivatives |
JP2001316361A (ja) * | 2000-05-01 | 2001-11-13 | Ethyl Corp | スクシンイミド−酸化合物およびそれの誘導体 |
ITMI20021537A1 (it) * | 2002-07-12 | 2004-01-12 | Ausimont Spa | Acidi immidoalcanpercarbossilici |
ITMI20040497A1 (it) * | 2004-03-16 | 2004-06-16 | Solvay Solexis Spa | Procedimento di diluizione |
CA2691442C (en) * | 2007-06-29 | 2014-01-21 | Gilead Sciences, Inc. | Antiviral compounds |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1793378C3 (de) * | 1968-09-09 | 1978-12-07 | Basf Ag, 6700 Ludwigshafen | N-Acyl-a-aminopercarbonsäuretert-butylester |
IT1233846B (it) * | 1988-01-20 | 1992-04-21 | Ausimont Spa | Perossiacidi immido aromatici |
DE3823172C2 (de) * | 1988-07-08 | 1998-01-22 | Hoechst Ag | omega-Phthalimidoperoxihexansäure, Verfahren zu dessen Herstellung und dessen Verwendung |
GB8830234D0 (en) * | 1988-12-24 | 1989-02-22 | Interox Chemicals Ltd | Peroxycarboxylic acids |
DE3906768A1 (de) * | 1989-03-03 | 1990-09-06 | Henkel Kgaa | Peroxycarbonsaeuren und deren verwendung |
-
1988
- 1988-10-24 IT IT8822402A patent/IT1230595B/it active
-
1989
- 1989-10-20 US US07/425,292 patent/US5536434A/en not_active Expired - Lifetime
- 1989-10-23 AU AU43640/89A patent/AU619607B2/en not_active Ceased
- 1989-10-23 DE DE68928767T patent/DE68928767T3/de not_active Expired - Fee Related
- 1989-10-23 CA CA002001184A patent/CA2001184A1/en not_active Abandoned
- 1989-10-23 EP EP89119644A patent/EP0366041B2/en not_active Expired - Lifetime
- 1989-10-23 AT AT89119644T patent/ATE169289T1/de active
- 1989-10-24 BR BR898905400A patent/BR8905400A/pt not_active Application Discontinuation
- 1989-10-24 KR KR1019890015292A patent/KR0140220B1/ko not_active IP Right Cessation
- 1989-10-24 JP JP1276989A patent/JP2915020B2/ja not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH02243671A (ja) | 1990-09-27 |
KR0140220B1 (ko) | 1998-06-01 |
EP0366041B1 (en) | 1998-08-05 |
IT1230595B (it) | 1991-10-28 |
DE68928767T3 (de) | 2002-05-08 |
ATE169289T1 (de) | 1998-08-15 |
IT8822402A0 (it) | 1988-10-24 |
DE68928767T2 (de) | 1999-04-15 |
US5536434A (en) | 1996-07-16 |
JP2915020B2 (ja) | 1999-07-05 |
CA2001184A1 (en) | 1990-04-24 |
AU619607B2 (en) | 1992-01-30 |
DE68928767D1 (de) | 1998-09-10 |
BR8905400A (pt) | 1990-05-22 |
EP0366041A3 (en) | 1991-10-23 |
EP0366041B2 (en) | 2001-09-12 |
EP0366041A2 (en) | 1990-05-02 |
AU4364089A (en) | 1990-04-26 |
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