AU2001268046A1 - Metathesis of functionalized allylic olefins - Google Patents
Metathesis of functionalized allylic olefinsInfo
- 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
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C253/00—Preparation of carboxylic acid nitriles
- C07C253/30—Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups
-
- 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
- B01J31/2265—Carbenes or carbynes, i.e.(image)
-
- 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
- B01J31/2265—Carbenes or carbynes, i.e.(image)
- B01J31/2269—Heterocyclic carbenes
- B01J31/2273—Heterocyclic carbenes with only nitrogen as heteroatomic ring members, e.g. 1,3-diarylimidazoline-2-ylidenes
-
- 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
- B01J31/24—Phosphines, 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
- B01J31/2404—Cyclic ligands, including e.g. non-condensed polycyclic ligands, the phosphine-P atom being a ring member or a substituent on the ring
-
- 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
- C07C29/32—Preparation 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
-
- 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
- B01J2231/50—Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds
- B01J2231/54—Metathesis reactions, e.g. olefin metathesis
- B01J2231/543—Metathesis reactions, e.g. olefin metathesis alkene metathesis
-
- 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
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) |
Families Citing this family (36)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
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)
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 |
-
2001
- 2001-05-04 US US09/849,100 patent/US6521799B2/en not_active Expired - Fee Related
- 2001-05-04 WO PCT/US2001/014378 patent/WO2001083097A2/en active Application Filing
- 2001-05-04 AU AU2001268046A patent/AU2001268046A1/en not_active Abandoned
-
2002
- 2002-08-23 US US10/227,127 patent/US6605748B2/en not_active Expired - Fee Related
- 2002-08-23 US US10/227,047 patent/US6559331B1/en not_active Expired - Fee Related
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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