CA2905209C - Metathesis catalysts and reactions using the catalysts - Google Patents

Metathesis catalysts and reactions using the catalysts Download PDF

Info

Publication number
CA2905209C
CA2905209C CA2905209A CA2905209A CA2905209C CA 2905209 C CA2905209 C CA 2905209C CA 2905209 A CA2905209 A CA 2905209A CA 2905209 A CA2905209 A CA 2905209A CA 2905209 C CA2905209 C CA 2905209C
Authority
CA
Canada
Prior art keywords
ipr
optionally substituted
phenyl
alkyl
compound
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.)
Active
Application number
CA2905209A
Other languages
English (en)
French (fr)
Other versions
CA2905209A1 (en
Inventor
Levente Ondi
Jeno VARGA
Agota Bucsai
Florian Toth
Krisztian LORINCZ
Csaba Hegedus
Emmanuel Robe
Geog FRATER
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.)
Verbio Vereinigte Bioenergie AG
Original Assignee
Verbio Vereinigte Bioenergie AG
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 Verbio Vereinigte Bioenergie AG filed Critical Verbio Vereinigte Bioenergie AG
Publication of CA2905209A1 publication Critical patent/CA2905209A1/en
Application granted granted Critical
Publication of CA2905209C publication Critical patent/CA2905209C/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

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
    • B01J31/22Organic complexes
    • B01J31/2265Carbenes or carbynes, i.e.(image)
    • 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
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/12Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
    • B01J31/14Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron
    • B01J31/143Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides of aluminium or boron of aluminium
    • 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
    • B01J31/1608Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes the ligands containing silicon
    • 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
    • B01J31/18Catalysts 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
    • B01J31/1805Catalysts 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
    • 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
    • B01J31/18Catalysts 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
    • B01J31/1805Catalysts 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
    • B01J31/181Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine
    • 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
    • B01J31/22Organic complexes
    • B01J31/2204Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208Oxygen, e.g. acetylacetonates
    • 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
    • B01J31/22Organic complexes
    • B01J31/2204Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208Oxygen, e.g. acetylacetonates
    • B01J31/2226Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
    • 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
    • B01J31/22Organic complexes
    • B01J31/2204Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208Oxygen, e.g. acetylacetonates
    • B01J31/2226Anionic ligands, i.e. the overall ligand carries at least one formal negative charge
    • B01J31/223At least two oxygen atoms present in one at least bidentate or bridging ligand
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C6/00Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
    • C07C6/02Metathesis reactions at an unsaturated carbon-to-carbon bond
    • C07C6/04Metathesis reactions at an unsaturated carbon-to-carbon bond at a carbon-to-carbon double bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/28Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/293Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/30Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/333Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • C07C67/343Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
    • C07C67/347Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by addition to unsaturated carbon-to-carbon bonds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F11/00Compounds containing elements of Groups 6 or 16 of the Periodic Table
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G61/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G61/02Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes
    • C08G61/04Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms
    • C08G61/06Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms prepared by ring-opening of carbocyclic compounds
    • C08G61/08Macromolecular compounds containing only carbon atoms in the main chain of the macromolecule, e.g. polyxylylenes only aliphatic carbon atoms prepared by ring-opening of carbocyclic compounds of carbocyclic compounds containing one or more carbon-to-carbon double bonds in the ring
    • 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
    • B01J2231/50Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds
    • B01J2231/54Metathesis reactions, e.g. olefin metathesis
    • B01J2231/543Metathesis reactions, e.g. olefin metathesis alkene metathesis
    • 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
    • B01J2531/02Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0286Complexes comprising ligands or other components characterized by their function
    • B01J2531/0288Sterically demanding or shielding ligands
    • 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
    • B01J2531/60Complexes comprising metals of Group VI (VIA or VIB) as the central metal
    • B01J2531/64Molybdenum
    • 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
    • B01J2531/60Complexes comprising metals of Group VI (VIA or VIB) as the central metal
    • B01J2531/66Tungsten
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2540/00Compositional aspects of coordination complexes or ligands in catalyst systems
    • B01J2540/20Non-coordinating groups comprising halogens
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2540/00Compositional aspects of coordination complexes or ligands in catalyst systems
    • B01J2540/20Non-coordinating groups comprising halogens
    • B01J2540/22Non-coordinating groups comprising halogens comprising fluorine, e.g. trifluoroacetate
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2540/00Compositional aspects of coordination complexes or ligands in catalyst systems
    • B01J2540/20Non-coordinating groups comprising halogens
    • B01J2540/22Non-coordinating groups comprising halogens comprising fluorine, e.g. trifluoroacetate
    • B01J2540/225Non-coordinating groups comprising halogens comprising fluorine, e.g. trifluoroacetate comprising perfluoroalkyl groups or moieties
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • C07C2531/12Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing organo-metallic compounds or metal hydrides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • C07C2531/22Organic complexes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/06Systems containing only non-condensed rings with a five-membered ring
    • C07C2601/10Systems containing only non-condensed rings with a five-membered ring the ring being unsaturated
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G2261/00Macromolecular compounds obtained by reactions forming a carbon-to-carbon link in the main chain of the macromolecule
    • C08G2261/40Polymerisation processes
    • C08G2261/41Organometallic coupling reactions
    • C08G2261/418Ring opening metathesis polymerisation [ROMP]

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Inorganic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
CA2905209A 2013-03-14 2014-03-13 Metathesis catalysts and reactions using the catalysts Active CA2905209C (en)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201361781120P 2013-03-14 2013-03-14
EP13001297.4 2013-03-14
US61/781,120 2013-03-14
EP13001297 2013-03-14
PCT/EP2014/000671 WO2014139679A2 (en) 2013-03-14 2014-03-13 Metathesis catalysts and reactions using the catalysts

Publications (2)

Publication Number Publication Date
CA2905209A1 CA2905209A1 (en) 2014-09-18
CA2905209C true CA2905209C (en) 2021-11-09

Family

ID=47912849

Family Applications (1)

Application Number Title Priority Date Filing Date
CA2905209A Active CA2905209C (en) 2013-03-14 2014-03-13 Metathesis catalysts and reactions using the catalysts

Country Status (7)

Country Link
US (3) US10343153B2 (cg-RX-API-DMAC7.html)
EP (2) EP3662996A3 (cg-RX-API-DMAC7.html)
JP (2) JP6636804B2 (cg-RX-API-DMAC7.html)
CN (1) CN105555402B (cg-RX-API-DMAC7.html)
BR (1) BR112015023269B8 (cg-RX-API-DMAC7.html)
CA (1) CA2905209C (cg-RX-API-DMAC7.html)
WO (1) WO2014139679A2 (cg-RX-API-DMAC7.html)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8362311B2 (en) 2009-09-30 2013-01-29 Massachusetts Institute Of Technology Highly Z-selective olefins metathesis
JP6636804B2 (ja) 2013-03-14 2020-01-29 フェルビオ フェルアイニクテ ビオエネルギー アクチェンゲゼルシャフト メタセシス触媒及び触媒を用いた反応
US20140330018A1 (en) * 2013-05-01 2014-11-06 Massachusetts Institute Of Technology Metathesis catalysts and methods thereof
EP3019510B1 (en) 2013-07-12 2020-12-02 Verbio Vereinigte BioEnergie AG Use of immobilized molybden- und tungsten-containing catalysts in olefin cross metathesis
US10427146B2 (en) 2013-10-01 2019-10-01 Ximo Ag Immobilized metathesis tungsten oxo alkylidene catalysts and use thereof in olefin metathesis
US9850268B2 (en) * 2014-11-05 2017-12-26 Trustees Of Boston College Metathesis catalysts and methods thereof
JP6583289B2 (ja) * 2014-12-26 2019-10-02 Agc株式会社 含塩素含フッ素オレフィンの製造方法
WO2016104518A1 (ja) * 2014-12-26 2016-06-30 旭硝子株式会社 オレフィンの製造方法
KR102483724B1 (ko) * 2015-03-09 2022-12-30 니폰 제온 가부시키가이샤 수지 성형체, 수지 필름, 및 사출 성형품
JP7186502B2 (ja) * 2015-03-09 2022-12-09 日本ゼオン株式会社 樹脂成形体の製造方法、樹脂フィルムの製造方法、及び射出成形品の製造方法
PL3377465T3 (pl) 2015-11-18 2024-02-12 Provivi, Inc. Wytwarzanie pochodnych olefin tłuszczowych przez metatezę olefin
BR112018010108A2 (pt) 2015-11-18 2018-11-21 Provivi Inc micro-organismos para a produção de ferormônios de inseto e compostos relacionados
EP3394074B1 (en) 2015-12-23 2019-10-09 XiMo AG Immobilized metal alkylidene catalysts and use thereof in olefin metathesis
GB201604110D0 (en) * 2016-03-10 2016-04-20 Givaudan Sa Preparation of macrocyclic lactones
US11214818B2 (en) 2016-06-06 2022-01-04 Provivi, Inc. Semi-biosynthetic production of fatty alcohols and fatty aldehydes
US11020730B2 (en) 2016-07-15 2021-06-01 Massachusetts Institute Of Technology Halogen-containing metathesis catalysts and methods thereof
WO2018150379A2 (en) 2017-02-17 2018-08-23 Provivi, Inc. Synthesis of pheromones and related materials via olefin metathesis
CN110914442B (zh) 2017-05-17 2025-02-18 普罗维维股份有限公司 用于产生昆虫信息素及相关化合物的微生物
WO2019060749A1 (en) 2017-09-22 2019-03-28 Trustees Of Boston College PROCESS FOR THE PREPARATION OF TRISUBSTITUTED ETHYLENE COMPOUNDS
US11702436B2 (en) 2018-03-22 2023-07-18 Verbio Vereinigte Bioenergie Ag Tetraphenylphenoxy tungsten oxo alkylidene complexes and methods of making same and use thereof
WO2020239859A1 (en) 2019-05-27 2020-12-03 Verbio Vereinigte Bioenergie Ag Tungsten imido alkylidene o-bitet and o-binol complexes and use thereof in olefin metathesis reactions
US10995049B2 (en) 2019-07-19 2021-05-04 California Institute Of Technology Total synthesis of prostaglandin J natural products and their intermediates
WO2021188337A1 (en) 2020-03-19 2021-09-23 Exxonmobil Chemical Patents Inc. Pentavalent dimeric group 6 transition metal complexes and methods for use thereof
JP2023528012A (ja) * 2020-05-27 2023-07-03 フェルビオ フェルアイニクテ ビオエネルギー アクチェンゲゼルシャフト 空気中で安定なイミドアルキリデン錯体及びオレフィンメタセシス反応におけるその使用
CN113980097B (zh) * 2021-12-29 2022-03-29 浙江湃肽生物有限公司南京分公司 棕榈酰三肽-5的纯化方法
CN114230702B (zh) * 2022-01-17 2023-10-13 万华化学集团股份有限公司 一种萘氧基骨架的烯烃聚合催化剂、制备方法与应用

Family Cites Families (59)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1037866A (en) * 1962-05-28 1966-08-03 Ethyl Corp Improved process for preparing alpha olefins of high vinyl olefin content
BE755794A (fr) * 1969-09-08 1971-03-08 Polymer Corp Procede de purification d'hydrocarbures olefiniques
US3689584A (en) * 1970-08-24 1972-09-05 Ethyl Corp A chemical process of separating olefins from aluminum alkyls by forming complexes of the aluminum alkyls which are insoluble in the olefins
US3696161A (en) * 1970-09-30 1972-10-03 Ethyl Corp A chemical process of separating hydrocarbyl aluminum from olefins by the use of 2:1 complexes of aluminum alkyls and an alkali metal salt
DE2845974A1 (de) * 1978-10-21 1980-04-30 Basf Ag Verfahren zur herstellung von carbonsaeureestern vicinaler glykole
IN160358B (cg-RX-API-DMAC7.html) 1983-01-10 1987-07-11 Thiokol Corp
US4637197A (en) 1984-10-15 1987-01-20 Epoxy Technology, Inc. Method and compositions for removal of moisture
JPH0428714A (ja) 1990-05-23 1992-01-31 Nippon Zeon Co Ltd 高重合活性ジシクロペンタジエンの製造法およびその重合法
US5210365A (en) 1990-08-27 1993-05-11 Shell Oil Company Olefin disproportionation catalyst and process
US5194534A (en) 1991-09-24 1993-03-16 Hercules Incorporated Tungsten-imido catalysts for ring-opening metathesis polymerization of cycloolefins
EP0864595B1 (en) 1997-03-13 2001-08-16 Borealis Technology Oy Supported catalysts for the ringopening metathesis polymerization of cycloolefins
DE19744102A1 (de) * 1997-10-06 1999-04-15 Targor Gmbh Katalysatorsystem
US6121473A (en) 1998-02-19 2000-09-19 Massachusetts Institute Of Technology Asymmetric ring-closing metathesis reactions
JP2004500364A (ja) * 1999-12-21 2004-01-08 サゾル テクノロジー(プロプライアタリー)リミティド 短鎖オレフィンを長鎖オレフィンに変換するための転換方法
US7411108B2 (en) * 2000-06-30 2008-08-12 Chevron Phillips Chemical Company Lp Process for the removal of conjugated olefins from a monoolefin stream
US6720468B2 (en) * 2000-06-30 2004-04-13 Chevron Phillips Chemical Company Lp Process for the removal of conjugated olefins from a monoolefin stream
US20050124839A1 (en) 2001-06-13 2005-06-09 Gartside Robert J. Catalyst and process for the metathesis of ethylene and butene to produce propylene
EP1501784B1 (en) 2002-04-29 2019-03-13 Dow Global Technologies LLC Integrated chemical processes for industrial utilization of seed oils
WO2005049672A1 (en) * 2003-11-14 2005-06-02 Exxonmobil Chemical Patents Inc. Transparent and translucent crosslinked propylenebased elastomers, and their production and use
US7813511B2 (en) 2005-07-01 2010-10-12 Cisco Technology, Inc. Facilitating mobility for a mobile station
US7932397B2 (en) 2006-11-22 2011-04-26 Massachusetts Institute Of Technology Olefin metathesis catalysts and related methods
US8642824B2 (en) * 2007-08-09 2014-02-04 Elevance Renewable Sciences, Inc. Chemical methods for treating a metathesis feedstock
US9284515B2 (en) 2007-08-09 2016-03-15 Elevance Renewable Sciences, Inc. Thermal methods for treating a metathesis feedstock
MX2010001615A (es) 2007-08-09 2010-04-22 Elevance Renewable Sciences Metodos termicos para tratar un material de alimentacion para la metatesis.
WO2009094201A2 (en) 2008-01-25 2009-07-30 Trustees Of Boston College Catalysts for metathesis reactons including enantioselective olefin metathesis, and related methods
JP5483940B2 (ja) 2009-07-13 2014-05-07 ユニ・チャーム株式会社 吸収体及び吸収性物品
US8222469B2 (en) 2009-07-15 2012-07-17 Massachusetts Institute Of Technology Catalysts and processes for the formation of terminal olefins by ethenolysis
US8362311B2 (en) * 2009-09-30 2013-01-29 Massachusetts Institute Of Technology Highly Z-selective olefins metathesis
US9222056B2 (en) 2009-10-12 2015-12-29 Elevance Renewable Sciences, Inc. Methods of refining natural oils, and methods of producing fuel compositions
US8735640B2 (en) 2009-10-12 2014-05-27 Elevance Renewable Sciences, Inc. Methods of refining and producing fuel and specialty chemicals from natural oil feedstocks
JP6224896B2 (ja) 2009-10-12 2017-11-01 エレバンス・リニューアブル・サイエンシズ,インコーポレーテッド 天然油供給原料から燃料を精製および製造する方法
US9051519B2 (en) * 2009-10-12 2015-06-09 Elevance Renewable Sciences, Inc. Diene-selective hydrogenation of metathesis derived olefins and unsaturated esters
JP5557536B2 (ja) 2010-01-26 2014-07-23 シンポ株式会社 油脂回収フィルター
EP2534140B1 (en) * 2010-02-08 2018-04-11 Trustees of Boston College Efficient methods for z- or cis-selective cross-metathesis
US8704029B2 (en) 2010-03-30 2014-04-22 Uop Llc Conversion of butylene to propylene under olefin metathesis conditions
US8993470B2 (en) 2010-04-03 2015-03-31 Studiengesellschaft Kohle Mbh Catalysts for the alkyne metathesis
US8722950B2 (en) * 2010-04-26 2014-05-13 Saudi Basic Industries Corporation Process for producing propylene and aromatics from butenes by metathesis and aromatization
US8935891B2 (en) 2011-06-09 2015-01-20 Uop Llc Olefin metathesis catalyst containing tungsten fluorine bonds
DE102011012629A1 (de) 2011-02-28 2012-08-30 Studiengesellschaft Kohle Mbh Metallkomplexe des Molybdäns und Wolframs und ihre Verwendung als Präkatalysatoren für die Olefinmetathese
JP2013014562A (ja) 2011-07-06 2013-01-24 Nippon Zeon Co Ltd タングステン錯体、メタセシス反応用触媒および環状オレフィン開環重合体の製造方法
EP2864447B3 (en) 2012-06-20 2019-07-17 Elevance Renewable Sciences, Inc. Natural oil metathesis compositions
EP2690838A1 (en) 2012-07-23 2014-01-29 Alcatel Lucent Authentification system preserving secret data confidentiality
EP2703081B1 (en) 2012-09-04 2019-08-07 XiMo AG Molybdenum and tungsten complexes as olefin metathesis catalysts and reactions using the catalysts
KR102202927B1 (ko) 2013-03-14 2021-01-14 윌마르 트레이딩 피티이 엘티디 처리된 복분해 기질 물질 및 이의 제조 및 사용 방법
WO2014150470A1 (en) 2013-03-14 2014-09-25 Elevance Renewable Sciences, Inc. Methods for treating a metathesis feedstock with metal alkoxides
JP6636804B2 (ja) 2013-03-14 2020-01-29 フェルビオ フェルアイニクテ ビオエネルギー アクチェンゲゼルシャフト メタセシス触媒及び触媒を用いた反応
EP3019510B1 (en) 2013-07-12 2020-12-02 Verbio Vereinigte BioEnergie AG Use of immobilized molybden- und tungsten-containing catalysts in olefin cross metathesis
WO2015003815A1 (en) 2013-07-12 2015-01-15 Ximo Ag Immobilized metathesis tungsten catalysts and use thereof in olefin metathesis
US10427146B2 (en) 2013-10-01 2019-10-01 Ximo Ag Immobilized metathesis tungsten oxo alkylidene catalysts and use thereof in olefin metathesis
WO2015108874A1 (en) 2014-01-16 2015-07-23 Elevance Renewable Sciences, Inc. Olefinic ester compositions and their use in oil- and gas-related applications
US9328055B2 (en) 2014-03-19 2016-05-03 Elevance Renewable Sciences, Inc. Systems and methods of refining natural oil feedstocks and derivatives thereof
GB201406591D0 (en) 2014-04-11 2014-05-28 Ximo Ag Compounds
DE102014105885A1 (de) 2014-04-25 2015-10-29 Universität Stuttgart N-Heterozyklische Carbenkomplexe von Metallimidoalkylidenen und Metalloxoalkylidenen und deren Verwendung
EP3233274A1 (en) 2014-12-17 2017-10-25 ETH Zürich Activation of supported olefin metathesis catalysts by organic reductants
US20170011038A1 (en) 2015-07-06 2017-01-12 David Revelle System and method for multiple factor sorting and user interface thereof
PL3377465T3 (pl) 2015-11-18 2024-02-12 Provivi, Inc. Wytwarzanie pochodnych olefin tłuszczowych przez metatezę olefin
DE102016122096A1 (de) 2016-11-17 2018-05-17 Universität Stuttgart Latente Katalysatoren zur vernetzenden Polymerisation von Dicyclopentadien (DCPD)
DE102017101431A1 (de) 2017-01-25 2018-07-26 Universität Stuttgart Molybdän- und Wolfram-Alkylidin-N-heterozyklische Carben-Komplexe
WO2018150379A2 (en) 2017-02-17 2018-08-23 Provivi, Inc. Synthesis of pheromones and related materials via olefin metathesis

Also Published As

Publication number Publication date
US20160030936A1 (en) 2016-02-04
BR112015023269B8 (pt) 2022-08-16
JP6636804B2 (ja) 2020-01-29
CA2905209A1 (en) 2014-09-18
CN105555402A (zh) 2016-05-04
US9919299B2 (en) 2018-03-20
EP3662996A2 (en) 2020-06-10
WO2014139679A3 (en) 2015-02-19
BR112015023269A2 (pt) 2017-07-18
US20140309466A1 (en) 2014-10-16
WO2014139679A2 (en) 2014-09-18
JP2018193379A (ja) 2018-12-06
JP2016510070A (ja) 2016-04-04
CN105555402B (zh) 2019-03-22
EP2969204A2 (en) 2016-01-20
US11285466B2 (en) 2022-03-29
WO2014139679A8 (en) 2014-12-11
BR112015023269B1 (pt) 2021-05-04
US10343153B2 (en) 2019-07-09
US20190366318A1 (en) 2019-12-05
EP3662996A3 (en) 2020-12-16

Similar Documents

Publication Publication Date Title
CA2905209C (en) Metathesis catalysts and reactions using the catalysts
AU2013294909B2 (en) Novel ruthenium complexes, their use in the metathesis reactions, and a process for carrying out the metathesis reaction
Schrock et al. Recent advances in the syntheses and applications of molybdenum and tungsten alkylidene and alkylidyne catalysts for the metathesis of alkenes and alkynes
JP7051918B2 (ja) オレフィンのクロスメタセシスを含む方法
WO2000002834A1 (en) Asymmetric metathesis reactions involving achiral and meso substrates
EP3019510A1 (en) Use of immobilized molybden- und tungsten-containing catalysts in olefin cross metathesis
EP2703081A1 (en) Molybdenum and tungsten complexes as olefin metathesis catalysts and reactions using the catalysts
EP3814363B1 (en) Organoruthenium complexes as precatalysts for olefin metathesis
Tkach et al. Palladium carboxylate/boron trifluoride etherate catalyst system for the selective dimerization of styrene
KR101540487B1 (ko) 알릴 화합물의 이성화 방법
Drăguţan et al. Immobilized ruthenium complexes bearing N, O-bidentate ligands
tom Dieck et al. Diazadiene-Controlled CC Coupling Reactions on Palladium and Iron
La Enantioselective synthesis through catalytic metathesis
Myagmarsuren et al. Novel palladium acetate based protocols for transformations of unsaturated hydrocarbons
Ge Reactivity of rare earth metal organometallics bearing ancillary ligands derived the 1, 4-Diazepan-6-amine framework
Gavenonis Tandem reactions of dienes generated by enyne metathesis
Gregory Block copolymer formation by transformation reactions
CA2973092A1 (en) Process for dehydrogenation of alkyl-containing compounds using molybdenum and tungsten nitrosyl complexes

Legal Events

Date Code Title Description
EEER Examination request

Effective date: 20181220