DE3469178D1 - Rhodium-phosphine complexes - Google Patents

Rhodium-phosphine complexes

Info

Publication number
DE3469178D1
DE3469178D1 DE8484306292T DE3469178T DE3469178D1 DE 3469178 D1 DE3469178 D1 DE 3469178D1 DE 8484306292 T DE8484306292 T DE 8484306292T DE 3469178 T DE3469178 T DE 3469178T DE 3469178 D1 DE3469178 D1 DE 3469178D1
Authority
DE
Germany
Prior art keywords
rhodium
phosphine complexes
phosphine
complexes
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.)
Expired
Application number
DE8484306292T
Other languages
English (en)
Inventor
Hidenori Kumobayashi
Susumu Akutagawa
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Takasago International Corp
Original Assignee
Takasago Perfumery Industry Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Takasago Perfumery Industry Co filed Critical Takasago Perfumery Industry Co
Application granted granted Critical
Publication of DE3469178D1 publication Critical patent/DE3469178D1/de
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/24Phosphines, i.e. phosphorus bonded to only carbon atoms, or to both carbon and hydrogen atoms, including e.g. sp2-hybridised phosphorus compounds such as phosphabenzene, phosphole or anionic phospholide ligands
    • B01J31/2404Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
    • B01J31/2442Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems
    • B01J31/2447Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as substituents on a ring of the condensed system or on a further attached ring
    • B01J31/2452Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring comprising condensed ring systems and phosphine-P atoms as substituents on a ring of the condensed system or on a further attached ring with more than one complexing phosphine-P atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C209/00Preparation of compounds containing amino groups bound to a carbon skeleton
    • C07C209/68Preparation of compounds containing amino groups bound to a carbon skeleton from amines, by reactions not involving amino groups, e.g. reduction of unsaturated amines, aromatisation, or substitution of the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
    • C07F15/0006Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
    • C07F15/0073Rhodium compounds
    • C07F15/008Rhodium compounds without a metal-carbon linkage
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/60Reduction reactions, e.g. hydrogenation
    • B01J2231/64Reductions in general of organic substrates, e.g. hydride reductions or hydrogenations
    • B01J2231/641Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes
    • B01J2231/645Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes of C=C or C-C triple bonds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/02Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0261Complexes comprising ligands with non-tetrahedral chirality
    • B01J2531/0266Axially chiral or atropisomeric ligands, e.g. bulky biaryls such as donor-substituted binaphthalenes, e.g. "BINAP" or "BINOL"
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/50Complexes comprising metals of Group V (VA or VB) as the central metal
    • B01J2531/52Antimony
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • B01J2531/822Rhodium

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
DE8484306292T 1983-09-16 1984-09-14 Rhodium-phosphine complexes Expired DE3469178D1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58169283A JPS6061587A (ja) 1983-09-16 1983-09-16 ロジウム−ホスフイン錯体

Publications (1)

Publication Number Publication Date
DE3469178D1 true DE3469178D1 (en) 1988-03-10

Family

ID=15883639

Family Applications (1)

Application Number Title Priority Date Filing Date
DE8484306292T Expired DE3469178D1 (en) 1983-09-16 1984-09-14 Rhodium-phosphine complexes

Country Status (4)

Country Link
US (1) US4605750A (de)
EP (1) EP0135392B1 (de)
JP (1) JPS6061587A (de)
DE (1) DE3469178D1 (de)

Families Citing this family (33)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS60199898A (ja) * 1984-03-22 1985-10-09 Takasago Corp ロジウム−ホスフイン錯体
JPS6127949A (ja) * 1984-07-17 1986-02-07 Takasago Corp 光学活性なエナミンの製造法
JPS62178594A (ja) * 1986-02-01 1987-08-05 Takasago Corp 新規ホスフイン化合物
ATE82745T1 (de) * 1986-08-21 1992-12-15 Hoffmann La Roche Verfahren zur herstellung von optisch aktiven enaminen oder von den entsprechenden aldehyden.
JPS63135397A (ja) * 1986-11-27 1988-06-07 Takasago Corp ルテニウム−ホスフイン錯体
JPS63145292A (ja) * 1986-12-09 1988-06-17 Takasago Corp ルテニウム−ホスフイン錯体
US4870208A (en) * 1988-06-03 1989-09-26 Monsanto Company Asymmetric hydrogenolysis of epoxides
JPH0692427B2 (ja) * 1989-07-11 1994-11-16 高砂香料工業株式会社 2,2’―ビス(ジシクロヘキシルホスフィノ)―6,6’―ジメチル―1,1’―ビフェニルを配位子とする錯体,およびその錯体を用いた有機カルボン酸とそのエステルの製造方法
JPH0768260B2 (ja) * 1990-03-01 1995-07-26 高砂香料工業株式会社 2,2’―ビス〔ジ―(3,5―ジアルキルフェニル)ホスフィノ〕―1,1’―ビナフチル及びこれを配位子とする遷移金属錯体
FR2666250A1 (fr) * 1990-09-05 1992-03-06 Rhone Poulenc Nutrition Animal Nouveaux catalyseurs, procede de preparation et leur utilisation.
JP2681057B2 (ja) * 1990-10-01 1997-11-19 高砂香料工業株式会社 2,2’―ビス(ジフェニルホスフィノ)―5,5’,6,6’,7,7’,8,8’―オクタヒドロ―1,1’―ビナフチル及びこれを配位子とする遷移金属錯体
JP2733880B2 (ja) * 1991-03-12 1998-03-30 高砂香料工業株式会社 光学活性三級ホスフィン化合物およびこれを配位子とする遷移金属錯体
US5191095A (en) * 1991-06-17 1993-03-02 Ethyl Corporation Asymmetric hydrogenation of olefinic amides using organoruthenium catalyst
US5187136A (en) * 1991-06-17 1993-02-16 Ethyl Corporation Asymmetric hydrogenation of aromatic-substituted olefins using organorhenium catalyst
US5202472A (en) * 1991-06-17 1993-04-13 Ethyl Corporation Asymmetric hydrogenation of aromatic-substituted olefins using organonickel catalyst
US5177231A (en) * 1991-06-17 1993-01-05 Ethyl Corporation Asymmetric hydrogenation of aromatic-substituted olefins using cationic ruthenium(III) complexes
US5190905A (en) * 1991-06-17 1993-03-02 Ethyl Corporation Asymmetric hydrogenation of aromatic-substituted olefins using metal or metal alloy catalysts
US5187281A (en) * 1991-06-17 1993-02-16 Ethyl Corporation Asymmetric hydrogenation of aromatic-substituted olefins using organoiridium catalyst
US5198576A (en) * 1991-08-26 1993-03-30 Ethyl Corporation Bicyclooctyl phosphines and catalysts thereof
US5736480A (en) * 1994-02-22 1998-04-07 California Institute Of Technology Supported phase chiral sulfonated BINAP catalyst solubilized in alcohol and method of asymmetric hydrogenation
US5935892A (en) * 1994-02-22 1999-08-10 California Institute Of Technology Supported phase catalyst
US6333435B1 (en) * 1995-05-18 2001-12-25 Merck & Co., Inc. Process of synthesizing binaphthyl derivatives
DE69913412T2 (de) * 1998-04-07 2004-09-16 Firmenich S.A. Stereospezifische Isomerisierung von Allylaminen unter Verwendung von Chiralen Phospho-Liganden
US6307087B1 (en) 1998-07-10 2001-10-23 Massachusetts Institute Of Technology Ligands for metals and improved metal-catalyzed processes based thereon
US7223879B2 (en) 1998-07-10 2007-05-29 Massachusetts Institute Of Technology Ligands for metals and improved metal-catalyzed processes based thereon
JP4275795B2 (ja) 1999-03-30 2009-06-10 高砂香料工業株式会社 ビニル基を有するホスフィン誘導体、それをモノマーとするポリマー及びそれらの遷移金属錯体
ATE297807T1 (de) * 1999-06-17 2005-07-15 Firmenich & Cie Stereospezifische isomerierung von allylaminen unter verwendung von immobilisierten chiralen phospho-liganden
DE10002976A1 (de) 2000-01-24 2001-07-26 Degussa Molekulargewichtsvergrößerte Liganden für asymmetrische homogen lösliche Hydrierkatalysatoren, Verfahren zu deren Herstellung und Verwendung
CN102665908A (zh) * 2009-09-28 2012-09-12 艾伯塔大学董事会 非均相铑金属催化剂
FR2952638A1 (fr) 2009-11-17 2011-05-20 Univ Strasbourg Procede de phosphination catalytique double ou triple de composes di, tri ou tetrahalobiaryles, intermediaires employes, composes obtenus et leurs utilisations
JP6054108B2 (ja) 2012-09-07 2016-12-27 高砂香料工業株式会社 光学活性2,3−ジヒドロファルネサールの製造方法
CN103254047B (zh) * 2013-05-29 2015-02-04 上海灏翔生物科技有限公司 制备L-薄荷醇中间体d-香茅醛的方法
CN111187326B (zh) * 2020-01-14 2022-04-19 上海灏翔生物科技有限公司 一种醋酸诺美孕酮的制备方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2116905A5 (fr) * 1970-12-10 1972-07-21 Inst Francais Du Petrole Nouveaux coordinats bidentes,leur fabrication et leurs applications
US3939188A (en) * 1972-03-24 1976-02-17 Exxon Research And Engineering Company Preparation of zerovalent phosphine substituted rhodium compounds and their use in the selective carbonylation of olefins
FR2230654B1 (de) * 1973-05-21 1975-11-21 Rhone Poulenc Ind
US4008281A (en) * 1973-12-03 1977-02-15 Monsanto Company Asymmetric catalysis
US4152344A (en) * 1977-08-08 1979-05-01 Celanese Corporation Phosphino-ferrocene ligands
US4201714A (en) * 1977-08-19 1980-05-06 Celanese Corporation Stabilized catalyst complex of rhodium metal, bidentate ligand and monodentate ligand
US4374278A (en) * 1980-02-28 1983-02-15 Union Carbide Corporation Hydroformylation catalyst reactivation
US4331818A (en) * 1980-03-19 1982-05-25 The Procter & Gamble Company Chiral phospine ligand
US4393240A (en) * 1981-07-06 1983-07-12 Stille John K Optically active phosphines

Also Published As

Publication number Publication date
EP0135392B1 (de) 1988-02-03
EP0135392A3 (en) 1985-06-12
JPS6061587A (ja) 1985-04-09
EP0135392A2 (de) 1985-03-27
JPH0145478B2 (de) 1989-10-03
US4605750A (en) 1986-08-12

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