AU2016357756B2 - Production of fatty olefin derivatives via olefin metathesis - Google Patents

Production of fatty olefin derivatives via olefin metathesis Download PDF

Info

Publication number
AU2016357756B2
AU2016357756B2 AU2016357756A AU2016357756A AU2016357756B2 AU 2016357756 B2 AU2016357756 B2 AU 2016357756B2 AU 2016357756 A AU2016357756 A AU 2016357756A AU 2016357756 A AU2016357756 A AU 2016357756A AU 2016357756 B2 AU2016357756 B2 AU 2016357756B2
Authority
AU
Australia
Prior art keywords
acetate
metathesis
formula
fatty
catalyst
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
AU2016357756A
Other languages
English (en)
Other versions
AU2016357756A1 (en
Inventor
Vu Bui
Pedro COELHO
Hasan MEHDI
Peter Meinhold
Keith M. Wampler
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.)
Provivi Inc
Original Assignee
Provivi Inc
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 Provivi Inc filed Critical Provivi Inc
Publication of AU2016357756A1 publication Critical patent/AU2016357756A1/en
Application granted granted Critical
Publication of AU2016357756B2 publication Critical patent/AU2016357756B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • 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)
    • B01J31/2278Complexes comprising two carbene ligands differing from each other, e.g. Grubbs second generation catalysts
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01PBIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
    • A01P19/00Pest attractants
    • 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
    • B01J31/2217At least one oxygen and one nitrogen atom present as complexing atoms in an at least bidentate or bridging ligand
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C11/00Aliphatic unsaturated hydrocarbons
    • C07C11/21Alkatrienes; Alkatetraenes; Other alkapolyenes
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C201/00Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
    • C07C201/02Preparation of esters of nitric acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C203/00Esters of nitric or nitrous acid
    • C07C203/02Esters of nitric acid
    • C07C203/04Esters of nitric acid having nitrate groups bound to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132Preparation 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
    • C07C29/136Preparation 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
    • C07C29/147Preparation 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 carboxylic acids or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C33/00Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C33/02Acyclic alcohols with carbon-to-carbon double bonds
    • C07C33/025Acyclic alcohols with carbon-to-carbon double bonds with only one double bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/27Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
    • C07C45/29Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/41Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by hydrogenolysis or reduction of carboxylic groups or functional derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C47/00Compounds having —CHO groups
    • C07C47/20Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
    • C07C47/21Unsaturated compounds having —CHO groups bound to acyclic carbon atoms with only carbon-to-carbon double bonds as unsaturation
    • 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
    • C07C67/08Preparation of carboxylic acid esters by reacting carboxylic acids or symmetrical anhydrides with the hydroxy or O-metal group of organic compounds
    • 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
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/02Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
    • C07C69/04Formic acid esters
    • C07C69/06Formic acid esters of monohydroxylic compounds
    • C07C69/07Formic acid esters of monohydroxylic compounds of unsaturated alcohols
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/02Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
    • C07C69/12Acetic acid esters
    • C07C69/14Acetic acid esters of monohydroxylic compounds
    • C07C69/145Acetic acid esters of monohydroxylic compounds of unsaturated alcohols
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/52Esters of acyclic unsaturated carboxylic acids having the esterified carboxyl group bound to an acyclic carbon atom
    • C07C69/533Monocarboxylic acid esters having only one carbon-to-carbon double bond
    • 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
    • B01J2531/60Complexes 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/09Geometrical isomers
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Inorganic Chemistry (AREA)
  • Materials Engineering (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • General Chemical & Material Sciences (AREA)
  • Plant Pathology (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
AU2016357756A 2015-11-18 2016-11-17 Production of fatty olefin derivatives via olefin metathesis Active AU2016357756B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201562257148P 2015-11-18 2015-11-18
US62/257,148 2015-11-18
PCT/US2016/062595 WO2017087710A2 (en) 2015-11-18 2016-11-17 Production of fatty olefin derivatives via olefin metathesis

Publications (2)

Publication Number Publication Date
AU2016357756A1 AU2016357756A1 (en) 2018-06-14
AU2016357756B2 true AU2016357756B2 (en) 2021-09-30

Family

ID=58689813

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2016357756A Active AU2016357756B2 (en) 2015-11-18 2016-11-17 Production of fatty olefin derivatives via olefin metathesis

Country Status (14)

Country Link
US (4) US9776179B2 (enExample)
EP (2) EP3377465B1 (enExample)
JP (2) JP6970088B2 (enExample)
CN (2) CN108473390B (enExample)
AR (2) AR108028A1 (enExample)
AU (1) AU2016357756B2 (enExample)
BR (1) BR112018009885B1 (enExample)
CA (1) CA3005562C (enExample)
CL (2) CL2018001337A1 (enExample)
HU (1) HUE063333T2 (enExample)
IL (1) IL259459B (enExample)
MX (1) MX2018006241A (enExample)
PL (1) PL3377465T3 (enExample)
WO (1) WO2017087710A2 (enExample)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2969204A2 (en) 2013-03-14 2016-01-20 XiMo AG Molybdenum and tungsten complexes as olefin metathesis catalysts and reactions using the catalysts
US10427146B2 (en) 2013-10-01 2019-10-01 Ximo Ag Immobilized metathesis tungsten oxo alkylidene catalysts and use thereof in olefin metathesis
GB201406591D0 (en) * 2014-04-11 2014-05-28 Ximo Ag Compounds
CN108473390B (zh) 2015-11-18 2022-08-09 普罗维维公司 通过烯烃复分解生产脂肪烯烃衍生物
HUE053613T2 (hu) 2015-11-18 2021-07-28 Provivi Inc Mikroorganizmusok rovarferomonok és kapcsolódó vegyületek elõállítására
AR110606A1 (es) 2016-06-06 2019-04-17 Provivi Inc Producción semi-biosintética de alcoholes grasos y aldehídos grasos
HUE073559T2 (hu) 2017-02-17 2026-01-28 Provivi Inc Feromonok és kapcsolódó anyagok szintézise olefin-metatézisen keresztül
JP7216018B2 (ja) 2017-05-17 2023-01-31 プロヴィヴィ インコーポレイテッド 昆虫フェロモンの生成のための微生物及び関連する化合物
JP2021520339A (ja) * 2018-03-22 2021-08-19 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 テトラフェニルフェノキシタングステンオキソアルキリデン複合体、その製造方法及びその使用
EP3823946A4 (en) 2018-07-16 2021-09-22 Provivi, Inc. SUMMARY OF STRAIGHT-CHAIN LEPIDOPTERA PHEROMONES BY APPROVAL OF ONE OR TWO CARBON ATOMS OF FAT ALKENES
US12049443B2 (en) 2018-12-10 2024-07-30 Provivi, Inc. Synthesis of conjugated diene pheromones and related compounds
CN113728082A (zh) * 2019-02-21 2021-11-30 丰益贸易私人有限公司 甘油酯低聚物的生产方法和由其形成的产品
CN114174310A (zh) 2019-05-27 2022-03-11 韦尔比奥联合生物能源股份公司 钨亚氨基亚烷基O-bitet和O-binol配合物及其在烯烃复分解反应中的用途
FI128954B (en) * 2019-09-26 2021-03-31 Neste Oyj Preparation of renewable base oil including metathesis
FI128953B (en) 2019-09-26 2021-03-31 Neste Oyj Production of renewable chemicals including metathesis and microbial oxidation
FI128952B (en) 2019-09-26 2021-03-31 Neste Oyj Preparation of renewable alkenes including metathesis
BR112022011440A2 (pt) 2019-12-11 2022-09-13 Novoloop Inc Composições e métodos para a degradação de polipropileno residual
WO2021247583A1 (en) * 2020-06-01 2021-12-09 Provivi, Inc. Synthesis of pheromone derivatives via z-selective olefin metathesis
JP7475264B2 (ja) * 2020-12-10 2024-04-26 信越化学工業株式会社 3-イソプロペニル-6-ヘプテナール化合物及び6-イソプロペニル-3-メチル-3,9-デカジエニル=カルボキシレート化合物の製造方法並びにその中間体
WO2025199154A1 (en) * 2024-03-18 2025-09-25 Provivi, Inc Synthesis of e pheromones
CN118852298B (zh) * 2024-09-24 2024-11-22 云南大学 一种制备线虫蛔糖苷和葡萄糖苷二聚信息素的方法

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6215019B1 (en) * 1998-09-01 2001-04-10 Tilliechem, Inc. Synthesis of 5-decenyl acetate and other pheromone components
US20020022741A1 (en) * 1998-09-01 2002-02-21 Pederson Richard L. Metathesis syntheses of pheromones or their components
US20130231499A1 (en) * 2012-03-05 2013-09-05 California Institute Of Technology Synthesis of z-olefin-containing lepidopteran insect pheromones
WO2014152309A1 (en) * 2013-03-14 2014-09-25 Materia, Inc. Use of soluble metal salts in metathesis reactions
WO2015155593A1 (en) * 2014-04-11 2015-10-15 Ximo Ag Compounds and the use thereof in metathesis reactions

Family Cites Families (71)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4231947A (en) 1979-01-02 1980-11-04 Massachusetts Institute Of Technology Tantalum and niobium catalysts or catalyst precursors
US4245131A (en) 1979-07-02 1981-01-13 Massachusetts Institute Of Technology Dimerization of olefins using tantalum and niobium catalysts
HU180386B (en) * 1980-10-24 1983-02-28 Egyt Gyogyszervegyeszeti Gyar Process for producing 11-dodecen-1-ol and 11-dodecen-1-yl-acetate of insect-feromone activity
US4427595A (en) 1981-07-16 1984-01-24 Massachusetts Institute Of Technology Catalyst composition to effect metathesis of acetylenes
US4560792A (en) * 1982-07-20 1985-12-24 Phillips Petroleum Company Disproportionation of functional olefins
DE3460103D1 (en) 1983-06-15 1986-05-28 Elf Aquitaine Catalyst for olefin methathesis
US4792620A (en) * 1983-10-14 1988-12-20 Bp Chemicals Limited Carbonylation catalysts
US4727215A (en) 1985-09-25 1988-02-23 Massachusetts Institute Of Technology Catalyst composition for effecting metathesis of olefins
US4681956A (en) 1985-09-25 1987-07-21 Massachusetts Institute Of Technology Catalyst composition for effecting metathesis of olefins
US4837358A (en) 1986-02-26 1989-06-06 Phillips Petroleum Company Preparation of 9-alkenyl ester compounds
US5081287A (en) * 1989-06-30 1992-01-14 Fmc Corporation Pesticidal polyhalo alkenoic acid esters
US5146033A (en) 1990-01-04 1992-09-08 Massachusetts Institute Of Technology Homogeneous rhenium catalysts for metathesis of olefins
US5087710A (en) 1990-01-04 1992-02-11 Massachusetts Institute Of Technology Homogeneous rhenium catalysts for metathesis of olefins
US5142073A (en) 1991-04-30 1992-08-25 Massachusetts Institute Of Technology Synthesis of molybdenum and tungsten complexes
DE4434640C1 (de) * 1994-09-28 1996-02-01 Hoechst Ag Verfahren zur Herstellung verbrückter Metallocene
SG72861A1 (en) 1997-09-30 2000-05-23 Kuraray Co Process for producing 7-octen-1-al
US6121473A (en) 1998-02-19 2000-09-19 Massachusetts Institute Of Technology Asymmetric ring-closing metathesis reactions
WO1999050211A1 (en) 1998-04-01 1999-10-07 Firmenich S.A. Reduction of carbonyl compounds by a silane in the presence of a zinc catalyst
DE19815275B4 (de) 1998-04-06 2009-06-25 Evonik Degussa Gmbh Alkylidenkomplexe des Rutheniums mit N-heterozyklischen Carbenliganden und deren Verwendung als hochaktive, selektive Katalysatoren für die Olefin-Metathese
US6346652B1 (en) 1998-07-13 2002-02-12 Massachusetts Institute Of Technology Asymmetric ring-closing metathesis reactions involving achiral and meso substrates
EP2116302B1 (en) 1998-09-10 2017-02-22 University Of New Orleans Foundation Catalyst complex with a heterocyclic carbene ligand
US6478081B1 (en) * 1999-08-04 2002-11-12 Apv North America Inc. Plate heat exchanger
CA2392049C (en) * 1999-11-18 2012-01-31 Richard L. Pederson Metathesis syntheses of pheromones or their components
US20040097745A9 (en) * 2001-03-30 2004-05-20 Grubbs Robert H. Cross-metathesis reaction of functionalized and substituted olefins using group 8 transition metal carbene complexes as metathesis catalysts
JP2004035452A (ja) * 2002-07-03 2004-02-05 Honshu Chem Ind Co Ltd 脂環式モノオレフィンメタノールの製造方法
EP1735352B1 (en) 2004-03-29 2019-08-21 California Institute Of Technology Latent, high-activity olefin metathesis catalysts containing an n-heterocyclic carbene ligand
GB0514612D0 (en) 2005-07-15 2005-08-24 Sasol Technology Uk Ltd The use of a phosphorus containing ligand and a cyclic organic ligand in a metathesis catalyst
EP1971616A1 (en) 2005-12-16 2008-09-24 Materia, Inc. Organometallic ruthenium complexes and related methods for the preparation of tetra-substituted and other hindered olefins
PL379879A1 (pl) 2006-06-07 2007-12-10 Umicore Ag & Co.Kg. Kompleksy rutenu i osmu, sposób ich wytwarzania oraz ich zastosowanie jako (pre)katalizatorów reakcji metatezy
DE102006043704A1 (de) 2006-09-18 2008-03-27 Umicore Ag & Co. Kg Neue Metathesekatalysatoren
WO2008140468A2 (en) * 2006-10-13 2008-11-20 Elevance Renewable Sciences, Inc. METHODS OF MAKING α, ω -DICARBOXYLIC ACID ALKENE DERIVATIVES BY METATHESIS
US7932397B2 (en) 2006-11-22 2011-04-26 Massachusetts Institute Of Technology Olefin metathesis catalysts and related methods
FR2909382B1 (fr) 2006-11-30 2009-01-23 Enscr Complexes catalytiques a base de ruthenium et utilisation de tels complexes pour la metathese d'olefines
DE102007020694A1 (de) 2007-05-03 2008-11-06 Evonik Degussa Gmbh Schwefelhaltige Metathesekatalysatoren
CN103951541A (zh) 2008-01-25 2014-07-30 波士顿学院董事会 用于催化包括对映选择性烯烃复分解的复分解反应的方法
EP2260047B2 (de) 2008-04-08 2016-07-20 Evonik Degussa GmbH Verfahren zur herstellung von ruthenium-carben-komplexen
EP2276745A4 (en) 2008-04-09 2013-02-27 Materia Inc N-HETEROCYCLIC CARBON LIGANDS WITH SUBSTITUTED SKELETON WEARING RUTHENIUM OLEFINMETATHESE CATALYSTS
WO2010037550A1 (en) 2008-10-04 2010-04-08 Umicore Ag & Co. Kg Method for preparation of ruthenium-indenylidene carbene catalysts
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
AP3604A (en) 2009-10-12 2016-02-25 Elevance Renewable Sciences Methods of refining and producing fuel from natural oil feedstocks
WO2011069134A2 (en) 2009-12-03 2011-06-09 Materia, Inc. Supported olefin metathesis catalysts
EP2361683A1 (en) 2010-01-29 2011-08-31 Umicore AG & Co. KG Process for preparation of ruthenium-based carbene catalysts with chelating alkylidene ligands
WO2011097642A1 (en) 2010-02-08 2011-08-11 Trustees Of Boston College Efficient methods for z- or cis-selective cross-metathesis
US8546500B2 (en) 2011-05-27 2013-10-01 Massachusetts Institute Of Technology Complexes for use in metathesis reactions
WO2012167171A2 (en) 2011-06-03 2012-12-06 Massachusetts Institute Of Technology Z-selective ring-closing metathesis reactions
PL216649B1 (pl) 2011-06-06 2014-04-30 Univ Warszawski Nowe kompleksy rutenu, sposób ich wytwarzania oraz zastosowanie w reakcji metatezy olefin
US9085595B2 (en) 2011-11-07 2015-07-21 Massachusetts Institute Of Technology Tungsten oxo alkylidene complexes for Z selective olefin metathesis
EP2639219B1 (en) 2012-03-14 2016-08-10 Umicore AG & Co. KG Ruthenium-based metathesis catalysts and precursors for their preparation
US20130281688A1 (en) 2012-04-24 2013-10-24 Elevance Renewable Sciences, Inc Unsaturated fatty alcohol compositions and derivatives from natural oil metathesis
GB201208589D0 (en) 2012-05-16 2012-06-27 Givaudan Sa Improvements in or relating to organic compounds
EP2679593B1 (en) 2012-06-26 2018-03-21 Umicore AG & Co. KG Method for preparation of a ruthenium indenylidene complex
US8642814B1 (en) * 2012-07-24 2014-02-04 Heliae Development, Llc Methods of converting mixtures of palmitoleic and oleic acid esters to high value products
DE112013004680T5 (de) 2012-09-25 2015-07-09 Modine Manufacturing Company Wärmetauscher
EP2725030A1 (en) 2012-10-29 2014-04-30 Umicore AG & Co. KG Ruthenium-based metathesis catalysts, precursors for their preparation and their use
BR112015019868B1 (pt) 2013-02-27 2020-06-09 Materia Inc composição de polimerização de metátese de abertura de anel (romp) e métodos para a produção de um artigo
EP2969204A2 (en) 2013-03-14 2016-01-20 XiMo AG Molybdenum and tungsten complexes as olefin metathesis catalysts and reactions using the catalysts
MY172163A (en) 2013-03-14 2019-11-15 Wilmar Trading Pte Ltd Methods for treating substrates prior to metathesis reactions, and methods for metathesizing substrates
US10173209B2 (en) 2013-03-15 2019-01-08 Dmitri Goussev Complex catalysts based on amino-phosphine ligands for hydrogenation and dehydrogenation processes
GB201305858D0 (en) 2013-03-28 2013-05-15 Ximo Ag Catalyst composition
WO2014169014A1 (en) 2013-04-09 2014-10-16 Massachusetts Institute Of Technology Metathesis catalysts and methods thereof
US9206211B2 (en) 2013-04-17 2015-12-08 Massachusetts Institute Of Technology Metathesis catalysts and methods thereof
US20140330018A1 (en) 2013-05-01 2014-11-06 Massachusetts Institute Of Technology Metathesis catalysts and methods thereof
WO2014201300A1 (en) 2013-06-12 2014-12-18 Trustees Of Boston College Catalysts for efficient z-selective metathesis
US9441059B2 (en) 2013-06-20 2016-09-13 Massachusetts Institute Of Technology Metathesis catalysts and methods thereof
US20160122375A1 (en) 2013-07-12 2016-05-05 Ximo Ag Immobilized metathesis tungsten catalysts and use thereof in olefin metathesis
WO2015003814A1 (en) 2013-07-12 2015-01-15 Ximo Ag Use of immobilized molybden- und tungsten-containing catalysts in olefin cross metathesis
CN103319704B (zh) 2013-07-12 2015-06-17 南开大学 一种用10-十一碳烯酸和香草酸制备聚酯的方法
EP3107655B1 (en) 2014-02-21 2024-05-08 Massachusetts Institute of Technology Catalysts and methods for ring opening metathesis polymerization
GB201404468D0 (en) 2014-03-13 2014-04-30 Givaudan Sa Process
CN108473390B (zh) 2015-11-18 2022-08-09 普罗维维公司 通过烯烃复分解生产脂肪烯烃衍生物

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6215019B1 (en) * 1998-09-01 2001-04-10 Tilliechem, Inc. Synthesis of 5-decenyl acetate and other pheromone components
US20020022741A1 (en) * 1998-09-01 2002-02-21 Pederson Richard L. Metathesis syntheses of pheromones or their components
US6696597B2 (en) * 1998-09-01 2004-02-24 Tilliechem, Inc. Metathesis syntheses of pheromones or their components
US20130231499A1 (en) * 2012-03-05 2013-09-05 California Institute Of Technology Synthesis of z-olefin-containing lepidopteran insect pheromones
WO2014152309A1 (en) * 2013-03-14 2014-09-25 Materia, Inc. Use of soluble metal salts in metathesis reactions
WO2015155593A1 (en) * 2014-04-11 2015-10-15 Ximo Ag Compounds and the use thereof in metathesis reactions

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
DENNIS S. BANASIAK, "Insect pheromones from olefin metathesis", JOURNAL OF MOLECULAR CATALYSIS, 1985, vol. 28, no. 1-3, pages 107-115 *
LEVISALLES JAQUES ET AL, "METATHESE D'ACETATES D'ALCOOLS o-INSATURES", TETRAHEDRON, (1980-01-01), vol. 36, no. 22, pages 3181 - 3185 *
PEDERSON RICHARD L ET AL, "Applications of olefin cross metathesis to commercial products", ADVANCED SYNTHESIS & CATALYSIS, vol. 344, no. 6-7, 2002, pages 728-735 *

Also Published As

Publication number Publication date
BR112018009885B1 (pt) 2021-09-21
US20170137365A1 (en) 2017-05-18
CN108473390A (zh) 2018-08-31
AR108028A1 (es) 2018-07-11
CN115215748A (zh) 2022-10-21
EP3377465B1 (en) 2023-08-02
US9776179B2 (en) 2017-10-03
WO2017087710A2 (en) 2017-05-26
JP7348939B2 (ja) 2023-09-21
EP3377465A2 (en) 2018-09-26
AU2016357756A1 (en) 2018-06-14
US11779911B2 (en) 2023-10-10
PL3377465T3 (pl) 2024-02-12
CL2018001337A1 (es) 2018-10-26
EP4234522A3 (en) 2023-10-25
BR112018009885A2 (pt) 2018-11-13
IL259459B (en) 2022-07-01
US20220032280A1 (en) 2022-02-03
WO2017087710A3 (en) 2017-08-17
EP4234522A2 (en) 2023-08-30
US10596562B2 (en) 2020-03-24
CA3005562A1 (en) 2017-05-26
EP3377465A4 (en) 2019-10-09
CN108473390B (zh) 2022-08-09
JP6970088B2 (ja) 2021-11-24
CL2019003183A1 (es) 2020-03-20
JP2022025109A (ja) 2022-02-09
CA3005562C (en) 2024-05-28
AR122037A2 (es) 2022-08-03
US20180099268A1 (en) 2018-04-12
US11077433B2 (en) 2021-08-03
JP2018535983A (ja) 2018-12-06
US20200261898A1 (en) 2020-08-20
HUE063333T2 (hu) 2024-01-28
IL259459A (en) 2018-07-31
MX2018006241A (es) 2018-11-09

Similar Documents

Publication Publication Date Title
AU2016357756B2 (en) Production of fatty olefin derivatives via olefin metathesis
EP3583088B1 (en) Synthesis of pheromones and related materials via olefin metathesis
US20190338317A1 (en) Microorganisms for the production of insect pheromones and related compounds
Boussalah et al. Antifungal activities of amino acid ester functional pyrazolyl compounds against Fusarium oxysporum f. sp. albedinis and Saccharomyces cerevisiae yeast
Bykov et al. Synthesis of natural compounds via the cycloolefin cometathesis with α-olefins
EP4157814B1 (en) Synthesis of pheromone derivatives via z-selective olefin metathesis
CN109953024B (zh) 梨圆蚧性信息素活性组合物、针对梨圆蚧的引诱剂、交配干扰器、吸引方法和交配干扰方法
CN107857782A (zh) 一种呋喃葡萄糖基三氮唑类化合物及其制备方法和杀菌剂
EP3823946A1 (en) Synthesis of straight-chain lepidopteran pheromones through one- or two- carbon homologation of fatty alkenes
Wöstemeyer 7 Disease Management of Phoma Infections
KATRAGUNTA C. GANESH KUMAR1, POORNIMA MONGOLLA1, 5, JAGADEESH BABU NANUBOLU2, PATHIPATI USHA RANI3, and

Legal Events

Date Code Title Description
DA2 Applications for amendment section 104

Free format text: THE NATURE OF THE AMENDMENT IS: AMEND THE NAME OF THE INVENTOR TO READ WAMPLER, KEITH M.; MEINHOLD, PETER; COELHO, PEDRO; BUI, VU AND MEHDI, HASA

DA3 Amendments made section 104

Free format text: THE NATURE OF THE AMENDMENT IS: AMEND THE NAME OF THE INVENTOR TO READ WAMPLER, KEITH M.; MEINHOLD, PETER; COELHO, PEDRO; BUI, VU AND MEHDI, HASAN

FGA Letters patent sealed or granted (standard patent)