AU2001276690A1 - Process for producing alcohol with transition metal complex having amide compound as ligand - Google Patents
Process for producing alcohol with transition metal complex having amide compound as ligandInfo
- Publication number
- AU2001276690A1 AU2001276690A1 AU2001276690A AU7669001A AU2001276690A1 AU 2001276690 A1 AU2001276690 A1 AU 2001276690A1 AU 2001276690 A AU2001276690 A AU 2001276690A AU 7669001 A AU7669001 A AU 7669001A AU 2001276690 A1 AU2001276690 A1 AU 2001276690A1
- Authority
- AU
- Australia
- Prior art keywords
- ligand
- transition metal
- metal complex
- amide compound
- producing alcohol
- Prior art date
- Legal status (The legal status 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 status listed.)
- Abandoned
Links
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 title 1
- -1 amide compound Chemical class 0.000 title 1
- 239000003446 ligand Substances 0.000 title 1
- 229910052723 transition metal Inorganic materials 0.000 title 1
- 150000003624 transition metals Chemical class 0.000 title 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/22—Organic complexes
- B01J31/2282—Unsaturated compounds used as ligands
- B01J31/2295—Cyclic compounds, e.g. cyclopentadienyls
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/18—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
- B01J31/1805—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
-
- 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
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
- C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
- C07C29/14—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of a —CHO group
-
- 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
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
- C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH
- C07C29/143—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. —COOH of ketones
-
- 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
- C07D207/04—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 no double bonds between ring members or between ring members and non-ring members
- C07D207/10—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 no 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
- C07D207/16—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
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/0046—Ruthenium compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/60—Reduction reactions, e.g. hydrogenation
- B01J2231/64—Reductions in general of organic substrates, e.g. hydride reductions or hydrogenations
- B01J2231/641—Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes
- B01J2231/643—Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes of R2C=O or R2C=NR (R= C, H)
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
- B01J2531/821—Ruthenium
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
- B01J2531/822—Rhodium
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Inorganic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2000-232725 | 2000-08-01 | ||
JP2000232725 | 2000-08-01 | ||
PCT/JP2001/006478 WO2002010101A1 (fr) | 2000-08-01 | 2001-07-27 | Procede de production d'un alcool en presence d'un complexe de metaux de transition contenant un compose amide en tant que liant |
Publications (1)
Publication Number | Publication Date |
---|---|
AU2001276690A1 true AU2001276690A1 (en) | 2002-02-13 |
Family
ID=18725360
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2001276690A Abandoned AU2001276690A1 (en) | 2000-08-01 | 2001-07-27 | Process for producing alcohol with transition metal complex having amide compound as ligand |
Country Status (3)
Country | Link |
---|---|
JP (1) | JP5041501B2 (fr) |
AU (1) | AU2001276690A1 (fr) |
WO (1) | WO2002010101A1 (fr) |
Families Citing this family (35)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2007182419A (ja) * | 2005-12-07 | 2007-07-19 | Tokyo Univ Of Science | プロリン誘導体及び光学活性アンチ選択性増強触媒 |
JP5169244B2 (ja) | 2007-03-22 | 2013-03-27 | 住友化学株式会社 | 新規還元酵素、その遺伝子、およびその利用法 |
JP5169243B2 (ja) | 2007-03-22 | 2013-03-27 | 住友化学株式会社 | 新規還元酵素、その遺伝子、およびその利用法 |
EP2172443B1 (fr) * | 2007-07-03 | 2013-03-27 | Hamari Chemicals, Ltd. | Procédé de fabrication d'une amine optiquement active |
WO2009039181A2 (fr) | 2007-09-17 | 2009-03-26 | State Of Oregon Acting By & Through The State Board Of Higher Education On Behalf Of Or. State Univ. | Organocatalyseurs à base de sulfonamide et procédé pour leur utilisation |
HUE031434T2 (en) * | 2009-02-16 | 2017-07-28 | Sumitomo Chemical Co | Process for the preparation of a phenylacetamide compound |
JP5719115B2 (ja) | 2009-03-12 | 2015-05-13 | 関東化学株式会社 | 新規な有機金属錯体およびアミン化合物の製造方法 |
JP2011201857A (ja) | 2010-03-03 | 2011-10-13 | Sumitomo Chemical Co Ltd | 植物病害防除組成物及び植物病害防除方法 |
JP5747542B2 (ja) * | 2010-03-03 | 2015-07-15 | 住友化学株式会社 | 植物病害防除組成物及び植物病害防除方法 |
JP5764957B2 (ja) | 2010-03-03 | 2015-08-19 | 住友化学株式会社 | 植物病害防除組成物及び植物病害防除方法 |
JP2011201850A (ja) | 2010-03-03 | 2011-10-13 | Sumitomo Chemical Co Ltd | 植物病害防除組成物及び植物病害防除方法 |
JP2011201852A (ja) | 2010-03-03 | 2011-10-13 | Sumitomo Chemical Co Ltd | 植物病害防除組成物及び植物病害防除方法 |
JP2011201853A (ja) | 2010-03-03 | 2011-10-13 | Sumitomo Chemical Co Ltd | 植物病害防除組成物及び植物病害防除方法 |
JP5793883B2 (ja) | 2010-03-03 | 2015-10-14 | 住友化学株式会社 | 植物病害防除組成物及び植物病害防除方法 |
JP5691595B2 (ja) | 2010-03-03 | 2015-04-01 | 住友化学株式会社 | 植物病害防除組成物及び植物病害防除方法 |
JP2011201856A (ja) | 2010-03-03 | 2011-10-13 | Sumitomo Chemical Co Ltd | 植物病害防除組成物及び植物病害防除方法 |
JP5799518B2 (ja) | 2010-03-03 | 2015-10-28 | 住友化学株式会社 | 植物病害防除組成物及び植物病害防除方法 |
JP5847386B2 (ja) | 2010-09-15 | 2016-01-20 | 関東化學株式会社 | アミン化合物の製造方法 |
JP5628613B2 (ja) | 2010-09-21 | 2014-11-19 | 高砂香料工業株式会社 | アミド化合物からアルコール及び/又はアミンを製造する方法 |
JP5793896B2 (ja) | 2010-10-07 | 2015-10-14 | 住友化学株式会社 | 植物病害防除組成物及び植物病害防除方法 |
JP2012097063A (ja) | 2010-10-07 | 2012-05-24 | Sumitomo Chemical Co Ltd | 植物病害防除組成物及び植物病害防除方法 |
JP2012102074A (ja) | 2010-10-14 | 2012-05-31 | Sumitomo Chemical Co Ltd | 有害生物防除用組成物及び有害生物防除方法 |
JP2012136503A (ja) | 2010-10-14 | 2012-07-19 | Sumitomo Chemical Co Ltd | 有害生物防除用組成物及び有害生物防除方法 |
JP2012102076A (ja) | 2010-10-14 | 2012-05-31 | Sumitomo Chemical Co Ltd | 有害生物防除用組成物及び有害生物防除方法 |
JP2012102075A (ja) | 2010-10-14 | 2012-05-31 | Sumitomo Chemical Co Ltd | 有害生物防除用組成物及び有害生物防除方法 |
JP2012102077A (ja) | 2010-10-14 | 2012-05-31 | Sumitomo Chemical Co Ltd | 有害生物防除用組成物及び有害生物防除方法 |
JP2012106984A (ja) | 2010-10-28 | 2012-06-07 | Sumitomo Chemical Co Ltd | 有害生物防除用組成物及び有害生物防除方法 |
JP2011137030A (ja) | 2011-03-01 | 2011-07-14 | Sumitomo Chemical Co Ltd | 有害生物防除組成物及び有害生物の防除方法。 |
US9108986B2 (en) * | 2011-07-15 | 2015-08-18 | Hamari Chemicals, Ltd. | Method for producing optically active tetrahydroquinolines |
WO2013061999A1 (fr) * | 2011-10-25 | 2013-05-02 | 浜理薬品工業株式会社 | Procédé de production d'alcool optiquement actif |
JP2014019680A (ja) | 2012-07-20 | 2014-02-03 | Sumitomo Chemical Co Ltd | 植物病害防除組成物およびその用途 |
JP6106976B2 (ja) | 2012-07-20 | 2017-04-05 | 住友化学株式会社 | 植物病害防除組成物およびその用途 |
BR112015013967A2 (pt) | 2012-12-21 | 2017-07-11 | Sumitomo Chemical Co | método para o aumento da produção de safras de sementes ou de frutas em número ou peso |
US9745229B2 (en) * | 2014-02-14 | 2017-08-29 | Takasago International Corporation | Method for producing optically active compound, and novel metal-diamine complex |
JP6890320B2 (ja) * | 2017-05-26 | 2021-06-18 | 国立研究開発法人産業技術総合研究所 | 二酸化炭素の水素化に用いる触媒、ギ酸製造方法、水素の貯蔵方法 |
Family Cites Families (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6187961B1 (en) * | 1997-11-06 | 2001-02-13 | Roche Vitamins Inc. | Process for the preparation of trans-(R,R)-actinol |
-
2001
- 2001-07-27 WO PCT/JP2001/006478 patent/WO2002010101A1/fr active Application Filing
- 2001-07-27 JP JP2002516234A patent/JP5041501B2/ja not_active Expired - Fee Related
- 2001-07-27 AU AU2001276690A patent/AU2001276690A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
WO2002010101A1 (fr) | 2002-02-07 |
JP5041501B2 (ja) | 2012-10-03 |
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