AU2001268046A1 - Metathesis of functionalized allylic olefins - Google Patents

Metathesis of functionalized allylic olefins

Info

Publication number
AU2001268046A1
AU2001268046A1 AU2001268046A AU6804601A AU2001268046A1 AU 2001268046 A1 AU2001268046 A1 AU 2001268046A1 AU 2001268046 A AU2001268046 A AU 2001268046A AU 6804601 A AU6804601 A AU 6804601A AU 2001268046 A1 AU2001268046 A1 AU 2001268046A1
Authority
AU
Australia
Prior art keywords
metathesis
functionalized allylic
allylic olefins
olefins
functionalized
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
Application number
AU2001268046A
Inventor
James Pawlow
John Sworen
Kenneth Wagener
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.)
University of Florida
Original Assignee
University of Florida
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 University of Florida filed Critical University of Florida
Publication of AU2001268046A1 publication Critical patent/AU2001268046A1/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00Preparation of carboxylic acid nitriles
    • C07C253/30Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups
    • 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
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/22Organic complexes
    • B01J31/2265Carbenes or carbynes, i.e.(image)
    • B01J31/2269Heterocyclic carbenes
    • B01J31/2273Heterocyclic carbenes with only nitrogen as heteroatomic ring members, e.g. 1,3-diarylimidazoline-2-ylidenes
    • 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
    • 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
    • C07C29/32Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions without formation of -OH groups
    • 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
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • B01J2531/821Ruthenium
AU2001268046A 2000-05-04 2001-05-04 Metathesis of functionalized allylic olefins Abandoned AU2001268046A1 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US20191800P 2000-05-04 2000-05-04
US60201918 2000-05-04
PCT/US2001/014378 WO2001083097A2 (en) 2000-05-04 2001-05-04 Metathesis of functionalized allylic olefins

Publications (1)

Publication Number Publication Date
AU2001268046A1 true AU2001268046A1 (en) 2001-11-12

Family

ID=22747827

Family Applications (1)

Application Number Title Priority Date Filing Date
AU2001268046A Abandoned AU2001268046A1 (en) 2000-05-04 2001-05-04 Metathesis of functionalized allylic olefins

Country Status (3)

Country Link
US (3) US6521799B2 (en)
AU (1) AU2001268046A1 (en)
WO (1) WO2001083097A2 (en)

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US6477252B1 (en) 1999-08-29 2002-11-05 Intel Corporation Digital video content transmission ciphering and deciphering method and apparatus
US6921736B1 (en) * 2000-07-17 2005-07-26 University Of New Orleans Research And Technology Foundation, Inc. Simply assembled and recyclable polymer-supported olefin metathesis catalysts
EP1395616B1 (en) 2001-04-16 2019-05-22 California Institute Of Technology Group 8 transition metal carbene complexes as enantioselective olefin metathesis catalysts
US6844409B2 (en) * 2002-05-06 2005-01-18 Kerr Corporation Composition curable by metathesis reaction
US7002049B2 (en) * 2002-08-19 2006-02-21 Eastman Chemical Company Process for α,β-dihydroxyalkenes and derivatives
US7173097B2 (en) * 2003-05-06 2007-02-06 Kerr Corporation Metathesis-curable composition with a reaction control agent
US7683148B2 (en) 2003-05-06 2010-03-23 Kerr Corporation Metathesis-curable composition with a reaction control agent
EP1543875A1 (en) * 2003-12-04 2005-06-22 Boehringer Ingelheim Pharma GmbH & Co. KG Novel metathesis ruthenium catalyst
DE102004033312A1 (en) * 2004-07-08 2006-01-26 Boehringer Ingelheim Pharma Gmbh & Co. Kg Continuous metathesis process with ruthenium catalysts
US7001590B1 (en) 2004-11-15 2006-02-21 Kerr Corporation Metathesis-curable composition
US7625551B2 (en) * 2004-11-15 2009-12-01 Kerr Corporation Polyether-based dental impression material curable by metathesis reaction
US7645443B2 (en) * 2004-11-15 2010-01-12 Kerr Corporation Polyether-based composition curable by metathesis reaction
US8101697B2 (en) * 2005-02-01 2012-01-24 Bridgestone Corporation Multi-functionalized high-trans elastomeric polymers
JP2007246900A (en) * 2006-02-21 2007-09-27 Kerr Corp Method for producing alkoxyl-siloxane polyether carboxylate terminal-blocked with functional olefin group
CN102227489B (en) 2008-11-26 2015-04-15 埃莱文斯可更新科学公司 Methods of producing jet fuel from natural oil feedstocks through oxygen-cleaved reactions
CA2742374C (en) 2008-11-26 2016-10-04 Elevance Renewable Sciences, Inc. Methods of producing jet fuel from natural oil feedstocks through metathesis reactions
MX2011011742A (en) * 2009-05-05 2011-12-08 Stepan Co Sulfonated internal olefin surfactant for enhanced oil recovery.
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
US9175231B2 (en) 2009-10-12 2015-11-03 Elevance Renewable Sciences, Inc. Methods of refining natural oils and methods of producing fuel compositions
US9382502B2 (en) 2009-10-12 2016-07-05 Elevance Renewable Sciences, Inc. Methods of refining and producing isomerized fatty acid esters and fatty acids from natural oil feedstocks
US9365487B2 (en) 2009-10-12 2016-06-14 Elevance Renewable Sciences, Inc. Methods of refining and producing dibasic esters and acids from natural oil feedstocks
US9169447B2 (en) 2009-10-12 2015-10-27 Elevance Renewable Sciences, Inc. Methods of refining natural oils, and methods of producing fuel compositions
US9051519B2 (en) 2009-10-12 2015-06-09 Elevance Renewable Sciences, Inc. Diene-selective hydrogenation of metathesis derived olefins and unsaturated esters
US9000246B2 (en) 2009-10-12 2015-04-07 Elevance Renewable Sciences, Inc. Methods of refining and producing dibasic esters and acids from natural oil feedstocks
US8957268B2 (en) 2009-10-12 2015-02-17 Elevance Renewable Sciences, Inc. Methods of refining natural oil feedstocks
US9222056B2 (en) 2009-10-12 2015-12-29 Elevance Renewable Sciences, Inc. Methods of refining natural oils, and methods of producing fuel compositions
US9139493B2 (en) 2011-12-22 2015-09-22 Elevance Renewable Sciences, Inc. Methods for suppressing isomerization of olefin metathesis products
US9133416B2 (en) 2011-12-22 2015-09-15 Elevance Renewable Sciences, Inc. Methods for suppressing isomerization of olefin metathesis products
US9169174B2 (en) 2011-12-22 2015-10-27 Elevance Renewable Sciences, Inc. Methods for suppressing isomerization of olefin metathesis products
US9388098B2 (en) 2012-10-09 2016-07-12 Elevance Renewable Sciences, Inc. Methods of making high-weight esters, acids, and derivatives thereof
FR3003564B1 (en) * 2013-03-19 2015-03-06 Arkema France METATHESIS METHOD COMPRISING THE EXTRACTION OF ETHYLENE FORMED USING A MEMBRANE
US20170190983A1 (en) * 2014-04-01 2017-07-06 Montana State University Process of converting natural plant oils to biofuels
FR3031517B1 (en) 2015-01-08 2018-08-17 Bostik Sa HYDROCARBON POLYMERS WITH TWO ALCOXYSILANE TERMINAL GROUPS
FR3051471A1 (en) 2016-05-17 2017-11-24 Bostik Sa HYDROCARBON POLYMERS WITH TWO ALCOXYSILANE TERMINAL GROUPS
FR3066763B1 (en) 2017-05-24 2019-06-28 Bostik Sa NOVEL HYDROCARBON COPOLYMERS LIQUID TO TWO ALCOXYSILANE TERMINAL GROUPS AND PROCESS FOR PREPARING THE SAME
FR3087442B1 (en) 2018-10-18 2020-10-02 Bostik Sa HYDROCARBON COPOLYMERS WITH ALTERNATE BLOCKS AND ALCOXYSILANE TERMINAL GROUPS

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6159890A (en) 1996-04-30 2000-12-12 Bp Amoco Corporation Ruthenium-containing catalyst system for olefin metathesis
US6156692A (en) * 1996-04-30 2000-12-05 Bp Amoco Corporation Ruthenium-containing catalyst composition for olefin metathesis
DE59702542D1 (en) * 1996-07-20 2000-11-30 Basf Ag METHOD FOR PRODUCING ALCOHOLS AND / OR ALDEHYDES FROM OLEFINS
US5917071A (en) 1996-11-15 1999-06-29 California Institute Of Technology Synthesis of ruthenium or osmium metathesis catalysts
US6215019B1 (en) * 1998-09-01 2001-04-10 Tilliechem, Inc. Synthesis of 5-decenyl acetate and other pheromone components
CA2361148C (en) 1999-01-26 2009-06-30 California Institute Of Technology Novel methods for cross-metathesis of terminal olefins

Also Published As

Publication number Publication date
US6521799B2 (en) 2003-02-18
WO2001083097A2 (en) 2001-11-08
US6559331B1 (en) 2003-05-06
US20030092928A1 (en) 2003-05-15
US20020058831A1 (en) 2002-05-16
US6605748B2 (en) 2003-08-12
WO2001083097A3 (en) 2002-03-21

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