ATE28869T1 - Chirale, optisch aktive verbindungen, verfahren zu ihrer herstellung und verwendung dieser verbindungen fuer den schutz funktioneller -oh, - sh, -nh-gruppen, zur racemattrennung, zur herstellung optisch aktiver imidoesterhydrochloride sowie optisch aktiver ester, zur herstellung optisch angereicherter alkohole und zur herstellung optisch aktiver verbindungen durch asymmetrische induktion. - Google Patents
Chirale, optisch aktive verbindungen, verfahren zu ihrer herstellung und verwendung dieser verbindungen fuer den schutz funktioneller -oh, - sh, -nh-gruppen, zur racemattrennung, zur herstellung optisch aktiver imidoesterhydrochloride sowie optisch aktiver ester, zur herstellung optisch angereicherter alkohole und zur herstellung optisch aktiver verbindungen durch asymmetrische induktion.Info
- Publication number
- ATE28869T1 ATE28869T1 AT82890185T AT82890185T ATE28869T1 AT E28869 T1 ATE28869 T1 AT E28869T1 AT 82890185 T AT82890185 T AT 82890185T AT 82890185 T AT82890185 T AT 82890185T AT E28869 T1 ATE28869 T1 AT E28869T1
- Authority
- AT
- Austria
- Prior art keywords
- optically active
- preparation
- compounds
- optically
- imidoester
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 6
- 230000006698 induction Effects 0.000 title abstract 2
- 238000000034 method Methods 0.000 title abstract 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 title 1
- -1 IMIDOESTER HYDROCHLORIDES Chemical class 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000926 separation method Methods 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000004122 cyclic group Chemical group 0.000 abstract 2
- 150000001241 acetals Chemical class 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 150000002148 esters Chemical class 0.000 abstract 1
- 150000002463 imidates Chemical class 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- UMRZSTCPUPJPOJ-KNVOCYPGSA-N norbornane Chemical group C1C[C@H]2CC[C@@H]1C2 UMRZSTCPUPJPOJ-KNVOCYPGSA-N 0.000 abstract 1
- 230000000707 stereoselective effect Effects 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
- C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D311/94—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems condensed with rings other than six-membered or with ring systems containing such rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/82—Purification; Separation; Stabilisation; Use of additives
- C07C209/86—Separation
- C07C209/88—Separation of optical isomers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/32—Separation; Purification; Stabilisation; Use of additives
- C07C253/34—Separation; Purification
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C257/00—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines
- C07C257/04—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines without replacement of the other oxygen atom of the carboxyl group, e.g. imino-ethers
- C07C257/06—Compounds containing carboxyl groups, the doubly-bound oxygen atom of a carboxyl group being replaced by a doubly-bound nitrogen atom, this nitrogen atom not being further bound to an oxygen atom, e.g. imino-ethers, amidines without replacement of the other oxygen atom of the carboxyl group, e.g. imino-ethers having carbon atoms of imino-carboxyl groups bound to hydrogen atoms, to acyclic carbon atoms, or to carbon atoms of rings other than six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
- C07C29/88—Separation; Purification; Use of additives, e.g. for stabilisation by treatment giving rise to a chemical modification of at least one compound
- C07C29/92—Separation; Purification; Use of additives, e.g. for stabilisation by treatment giving rise to a chemical modification of at least one compound by a consecutive conversion and reconstruction
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/02—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of thiols
- C07C319/12—Preparation of thiols, sulfides, hydropolysulfides or polysulfides of thiols by reactions not involving the formation of mercapto groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C319/00—Preparation of thiols, sulfides, hydropolysulfides or polysulfides
- C07C319/26—Separation; Purification; Stabilisation; Use of additives
- C07C319/28—Separation; Purification
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/77—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
- C07D307/93—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems condensed with a ring other than six-membered
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2602/00—Systems containing two condensed rings
- C07C2602/02—Systems containing two condensed rings the rings having only two atoms in common
- C07C2602/04—One of the condensed rings being a six-membered aromatic ring
- C07C2602/10—One of the condensed rings being a six-membered aromatic ring the other ring being six-membered, e.g. tetraline
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Furan Compounds (AREA)
- Epoxy Compounds (AREA)
- Pyrane Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AT545381 | 1981-12-18 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE28869T1 true ATE28869T1 (de) | 1987-08-15 |
Family
ID=3575963
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT82890185T ATE28869T1 (de) | 1981-12-18 | 1982-12-17 | Chirale, optisch aktive verbindungen, verfahren zu ihrer herstellung und verwendung dieser verbindungen fuer den schutz funktioneller -oh, - sh, -nh-gruppen, zur racemattrennung, zur herstellung optisch aktiver imidoesterhydrochloride sowie optisch aktiver ester, zur herstellung optisch angereicherter alkohole und zur herstellung optisch aktiver verbindungen durch asymmetrische induktion. |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US4497960A (enExample) |
| EP (1) | EP0083335B1 (enExample) |
| JP (1) | JPS58159485A (enExample) |
| AT (1) | ATE28869T1 (enExample) |
| DE (1) | DE3276938D1 (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2517677B1 (fr) * | 1981-12-09 | 1986-05-16 | Roussel Uclaf | Nouveaux ethers dont les restes organiques comportent des atomes chiraux, leur procede de preparation et leur application au dedoublement des alcools ou de certains composes de structure hemiacetalique. |
| AT379812B (de) * | 1984-04-04 | 1986-03-10 | Noe Christian | Verfahren zur herstellung enantiomerenreiner pheromone |
| AT385983B (de) * | 1985-06-03 | 1988-06-10 | Loba Feinchemie Ges M B H | Eine analytische methode und reagenzien zur bestimmung der absolutkonfiguration und des enantiomerengehaltes optisch aktiver verbindungen |
| AU5527190A (en) * | 1989-04-24 | 1990-11-16 | Max Knollmuller | Acetalically protected, enantiomer-pure alpha-arylalkane carboxylic acids, their production and use |
| WO1990012794A1 (de) * | 1989-04-24 | 1990-11-01 | Noe Christian R | Enantiomerenreine am sauerstoff acetalisch geschützte 1,2-aminoalkohole, deren herstellung und verwendung |
| AT396686B (de) * | 1992-04-13 | 1993-11-25 | Christian Dr Noe | Reagention zur razemattrennung, verfahren zu ihrer herstellung und verwendung |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH621706A5 (enExample) * | 1977-06-17 | 1981-02-27 | Firmenich & Cie | |
| US4223167A (en) * | 1978-02-14 | 1980-09-16 | Fritzsche Dodge & Olcott Inc. | Processes for preparing β-santalol, β-santalene dihydro-β-santalol and related compounds |
| FR2423488A1 (fr) * | 1978-03-17 | 1979-11-16 | Roussel Uclaf | Nouveaux ethers dont les restes organiques comportent des atomes chiraux, leur procede de preparation et leur application au dedoublement des alcools, des phenols ou de certains composes de structure lactonique |
| EP0066684B1 (fr) * | 1981-05-21 | 1984-08-08 | Firmenich Sa | Composés tricycliques oxygénés dérivés du norbornane et leur utilisation en tant qu'ingrédients parfumants |
-
1982
- 1982-12-06 US US06/446,944 patent/US4497960A/en not_active Expired - Fee Related
- 1982-12-17 AT AT82890185T patent/ATE28869T1/de not_active IP Right Cessation
- 1982-12-17 EP EP82890185A patent/EP0083335B1/de not_active Expired
- 1982-12-17 DE DE8282890185T patent/DE3276938D1/de not_active Expired
- 1982-12-18 JP JP57221132A patent/JPS58159485A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0242831B2 (enExample) | 1990-09-26 |
| JPS58159485A (ja) | 1983-09-21 |
| US4497960A (en) | 1985-02-05 |
| EP0083335A1 (de) | 1983-07-06 |
| EP0083335B1 (de) | 1987-08-12 |
| DE3276938D1 (en) | 1987-09-17 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| REN | Ceased due to non-payment of the annual fee |