ATE469909T1 - Als katalysator für die asymmetrische transferhydrierung geeignete chirale verbindung - Google Patents
Als katalysator für die asymmetrische transferhydrierung geeignete chirale verbindungInfo
- Publication number
- ATE469909T1 ATE469909T1 AT05803818T AT05803818T ATE469909T1 AT E469909 T1 ATE469909 T1 AT E469909T1 AT 05803818 T AT05803818 T AT 05803818T AT 05803818 T AT05803818 T AT 05803818T AT E469909 T1 ATE469909 T1 AT E469909T1
- Authority
- AT
- Austria
- Prior art keywords
- chiral compound
- catalyst
- bidentate ligand
- transfer hydrogenation
- asymmetric transfer
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 5
- 239000003054 catalyst Substances 0.000 title abstract 3
- 238000009901 transfer hydrogenation reaction Methods 0.000 title abstract 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 4
- 239000003446 ligand Substances 0.000 abstract 4
- 229910052751 metal Inorganic materials 0.000 abstract 4
- 239000002184 metal Substances 0.000 abstract 4
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 2
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 abstract 2
- KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 abstract 2
- 229910017052 cobalt Inorganic materials 0.000 abstract 2
- 239000010941 cobalt Substances 0.000 abstract 2
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 abstract 2
- 229910052741 iridium Inorganic materials 0.000 abstract 2
- GKOZUEZYRPOHIO-UHFFFAOYSA-N iridium atom Chemical compound [Ir] GKOZUEZYRPOHIO-UHFFFAOYSA-N 0.000 abstract 2
- 229910052742 iron Inorganic materials 0.000 abstract 2
- 150000002739 metals Chemical class 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 229910052762 osmium Inorganic materials 0.000 abstract 2
- SYQBFIAQOQZEGI-UHFFFAOYSA-N osmium atom Chemical compound [Os] SYQBFIAQOQZEGI-UHFFFAOYSA-N 0.000 abstract 2
- 230000000737 periodic effect Effects 0.000 abstract 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 abstract 2
- 229910052703 rhodium Inorganic materials 0.000 abstract 2
- 239000010948 rhodium Substances 0.000 abstract 2
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 abstract 2
- 229910052707 ruthenium Inorganic materials 0.000 abstract 2
- 229910052723 transition metal Inorganic materials 0.000 abstract 2
- 150000003624 transition metals Chemical class 0.000 abstract 2
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 239000000852 hydrogen donor Substances 0.000 abstract 1
- 229910052759 nickel Inorganic materials 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 229910052763 palladium Inorganic materials 0.000 abstract 1
- 229910052697 platinum Inorganic materials 0.000 abstract 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 1
- 125000000467 secondary amino group Chemical group [H]N([*:1])[*:2] 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F17/00—Metallocenes
- C07F17/02—Metallocenes of metals of Groups 8, 9 or 10 of the Periodic Table
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04078106 | 2004-11-11 | ||
| PCT/EP2005/012198 WO2006050988A1 (en) | 2004-11-11 | 2005-11-10 | Chiral compound suitable as a catalyst for asymmetric transfer hydrogenation |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE469909T1 true ATE469909T1 (de) | 2010-06-15 |
Family
ID=34928654
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT05803818T ATE469909T1 (de) | 2004-11-11 | 2005-11-10 | Als katalysator für die asymmetrische transferhydrierung geeignete chirale verbindung |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US7884223B2 (de) |
| EP (1) | EP1824868B1 (de) |
| JP (1) | JP2008519798A (de) |
| CN (1) | CN101072786B (de) |
| AT (1) | ATE469909T1 (de) |
| DE (1) | DE602005021686D1 (de) |
| WO (1) | WO2006050988A1 (de) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2010102003A2 (en) * | 2009-03-03 | 2010-09-10 | Vanderbilt University | Alkylsulfonyl-2,3-dihydrospiro[indene-1,4'-piperidine] analogs as glyt1 inhibitors, methods for making same, and use of same in treating psychiatric disorders |
| CN109970533B (zh) * | 2012-12-18 | 2022-06-14 | 帝斯曼知识产权资产管理有限公司 | 由(r)-6，10，14-三甲基十五碳-5-烯-2-酮制备的(6r，10r)-6，10，14-三甲基十五烷-2-酮 |
| CN104045568A (zh) * | 2014-06-18 | 2014-09-17 | 中山奕安泰医药科技有限公司 | 一种合成(r)-1–(萘-1-基)乙胺的新工艺 |
| CN113941365B (zh) * | 2021-10-11 | 2023-09-01 | 南开沧州渤海新区绿色化工研究有限公司 | 用于芳香酮不对称氢转移反应的温敏催化剂及其制备方法 |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0916637B1 (de) * | 1995-12-06 | 2005-04-20 | Japan Science and Technology Agency | Verfahren zur herstellung optische aktive verbindungen |
-
2005
- 2005-11-10 JP JP2007540604A patent/JP2008519798A/ja not_active Withdrawn
- 2005-11-10 DE DE602005021686T patent/DE602005021686D1/de not_active Expired - Lifetime
- 2005-11-10 US US11/667,381 patent/US7884223B2/en active Active
- 2005-11-10 CN CN200580041798.3A patent/CN101072786B/zh not_active Expired - Lifetime
- 2005-11-10 WO PCT/EP2005/012198 patent/WO2006050988A1/en not_active Ceased
- 2005-11-10 AT AT05803818T patent/ATE469909T1/de active
- 2005-11-10 EP EP05803818A patent/EP1824868B1/de not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| WO2006050988A1 (en) | 2006-05-18 |
| EP1824868A1 (de) | 2007-08-29 |
| CN101072786B (zh) | 2015-11-25 |
| JP2008519798A (ja) | 2008-06-12 |
| CN101072786A (zh) | 2007-11-14 |
| US7884223B2 (en) | 2011-02-08 |
| EP1824868B1 (de) | 2010-06-02 |
| DE602005021686D1 (de) | 2010-07-15 |
| US20080269529A1 (en) | 2008-10-30 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Zhang et al. | Asymmetric transfer and pressure hydrogenation with earth‐abundant transition metal catalysts | |
| Loup et al. | Asymmetric Iron‐Catalyzed C− H Alkylation Enabled by Remote Ligand meta‐Substitution | |
| Liu et al. | Base-metal-catalyzed olefin isomerization reactions | |
| Nishibayashi et al. | Extremely high enantioselective redox reaction of ketones and alcohols catalyzed by RuCl2 (PPh3)(oxazolinylferrocenylphosphine) | |
| MY121112A (en) | Raney iron catalyst and a process for hydrogenating organic compounds using said catalyst. | |
| Sortais et al. | Cycloruthenated primary and secondary amines as efficient catalyst precursors for asymmetric transfer hydrogenation | |
| EP1561741A4 (de) | Verfahren zur deuterierung oder tritiierung eines heterocyclus | |
| Patureau et al. | Sulfonamido− phosphoramidite ligands in cooperative dinuclear hydrogenation catalysis | |
| WO2002051779A3 (de) | Verfahren zur herstellung von alkoholen durch hydrierung von carbonylverbindungen | |
| ATE15649T1 (de) | Verfahren zur herstellung von cycloaliphatischen und/oder aromatischen aminen. | |
| ATE368020T1 (de) | Transferhydrierungsverfahren und katalysator | |
| AU2011219264B2 (en) | Process for production of activated Fischer-Tropsch synthesis catalyst, and process for production of hydrocarbon | |
| EA201170184A1 (ru) | Способ разложения no, катализатор для него и способ получения такого катализатора | |
| Hopmann | Iron/Brønsted Acid Catalyzed Asymmetric Hydrogenation: Mechanism and Selectivity‐Determining Interactions | |
| HRP20010513B1 (en) | Method for producing l-phenylephrine hydrochloride | |
| Lu et al. | Earth-abundant transition metal catalyzed asymmetric hydrogenation of minimally functionalized alkenes | |
| ATE469909T1 (de) | Als katalysator für die asymmetrische transferhydrierung geeignete chirale verbindung | |
| Kitamura et al. | Mechanistic insight into NOYORI asymmetric hydrogenations | |
| UA109641C2 (ru) | Получение углеводородов | |
| MXPA02012519A (es) | Ferrocenil-difosfinas y su uso. | |
| IL164915A (en) | Process for hydrogenating unactivated imines using ruthenium complexes as catalysts | |
| Ito et al. | Amine-Assisted C− Cl Bond Activation of Aryl Chlorides by a (Phebox) Rh-Chloro Complex | |
| Phillips et al. | A new class of rhodium (I) κ1-P and κ2-P, N complexes with rigid PTN (R) ligands (PTN= 7-phospha-3-methyl-1, 3, 5-triazabicyclo [3.3. 1] nonane) | |
| Anderson et al. | The synthesis of new planar chiral heterobidentate chelate ligands for asymmetric catalysis | |
| HRP20080145T3 (en) | Asymmetric hydrogenation process useful for the preparation of cycloalkanoindole derivatives |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| UEP | Publication of translation of european patent specification |
Ref document number: 1824868 Country of ref document: EP |