AU1921201A - Metathesis syntheses of pheromones or their components - Google Patents

Metathesis syntheses of pheromones or their components

Info

Publication number
AU1921201A
AU1921201A AU19212/01A AU1921201A AU1921201A AU 1921201 A AU1921201 A AU 1921201A AU 19212/01 A AU19212/01 A AU 19212/01A AU 1921201 A AU1921201 A AU 1921201A AU 1921201 A AU1921201 A AU 1921201A
Authority
AU
Australia
Prior art keywords
pheromone
omega
syntheses
acetate
moth
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
AU19212/01A
Other languages
English (en)
Inventor
Robert H. Grubbs
Richard L. Pederson
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.)
RICHARD L PEDERSON
Original Assignee
RICHARD L PEDERSON
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 RICHARD L PEDERSON filed Critical RICHARD L PEDERSON
Publication of AU1921201A publication Critical patent/AU1921201A/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/50Organo-phosphines
    • C07F9/505Preparation; Separation; Purification; Stabilisation
    • C07F9/5086Preparation; Separation; Purification; Stabilisation from phosphonium salts as starting materials
    • 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
    • C07C29/09Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis
    • C07C29/095Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by hydrolysis of esters of organic acids
    • 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
    • C07C29/44Preparation 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 addition reactions, i.e. reactions involving at least one carbon-to-carbon double or triple 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
    • C07C45/51Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
    • C07C45/511Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups
    • C07C45/515Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups the singly bound functional group being an acetalised, ketalised hemi-acetalised, or hemi-ketalised hydroxyl group
    • 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
    • C07C67/12Preparation of carboxylic acid esters from asymmetrical anhydrides
    • 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
    • C07C67/28Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/297Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/475Preparation of carboxylic acid esters by splitting of carbon-to-carbon bonds and redistribution, e.g. disproportionation or migration of groups between different molecules
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • C07F5/02Boron compounds
    • C07F5/025Boronic and borinic acid compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • C07F5/02Boron compounds
    • C07F5/04Esters of boric acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/09Geometrical isomers
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/582Recycling of unreacted starting or intermediate materials

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)
  • Pyrane Compounds (AREA)
AU19212/01A 1999-11-18 2000-11-17 Metathesis syntheses of pheromones or their components Abandoned AU1921201A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US16654399P 1999-11-18 1999-11-18
US60166543 1999-11-18
PCT/US2000/031549 WO2001036368A2 (en) 1999-11-18 2000-11-17 Metathesis syntheses of pheromones or their components

Publications (1)

Publication Number Publication Date
AU1921201A true AU1921201A (en) 2001-05-30

Family

ID=22603759

Family Applications (1)

Application Number Title Priority Date Filing Date
AU19212/01A Abandoned AU1921201A (en) 1999-11-18 2000-11-17 Metathesis syntheses of pheromones or their components

Country Status (11)

Country Link
EP (1) EP1230207B1 (enExample)
JP (2) JP4943612B2 (enExample)
CN (1) CN100528829C (enExample)
AT (1) ATE298318T1 (enExample)
AU (1) AU1921201A (enExample)
BR (1) BR0015712B1 (enExample)
CA (1) CA2392049C (enExample)
DE (1) DE60020987T2 (enExample)
IL (2) IL149720A0 (enExample)
WO (1) WO2001036368A2 (enExample)
ZA (1) ZA200204712B (enExample)

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CA2442368C (en) 2001-03-30 2015-10-13 California Institute Of Technology Cross-metathesis reaction of functionalized and substituted olefins using group 8 transition metal carbene complexes as metathesis catalysts
CA2512815A1 (en) 2003-01-13 2004-07-29 Cargill, Incorporated Method for making industrial chemicals
AU2006205023C1 (en) 2005-01-10 2012-05-24 Elevance Renewable Sciences, Inc. Candle and candle wax containing metathesis and metathesis-like products
RU2435778C2 (ru) * 2005-07-04 2011-12-10 Заннан Сайтех Ко., Лтд. Лиганд комплекса рутения, комплекс рутения, катализатор комплекса рутения и способы его получения и применения
WO2007081987A2 (en) * 2006-01-10 2007-07-19 Elevance Renewable Sciences, Inc. Method of making hydrogenated metathesis products
WO2007103460A2 (en) 2006-03-07 2007-09-13 Elevance Renewable Sciences, Inc. Colorant compositions comprising metathesized unsaturated polyol esters
PL220777B1 (pl) 2006-03-07 2016-01-29 Elevance Renewable Sciences Kompozycja typu wazeliny i jej zastosowanie oraz emulsja zawierająca zdyspergowaną fazę i jej zastosowanie
WO2008008420A1 (en) 2006-07-12 2008-01-17 Elevance Renewable Sciences, Inc. Hot melt adhesive compositions comprising metathesized unsaturated polyol ester wax
US8067610B2 (en) 2006-07-13 2011-11-29 Yann Schrodi Synthesis of terminal alkenes from internal alkenes and ethylene via olefin metathesis
CN101129138B (zh) * 2006-08-25 2010-06-23 北京中捷四方生物科技有限公司 一种思茅松毛虫性引诱剂和诱芯及其制备方法
WO2008140468A2 (en) 2006-10-13 2008-11-20 Elevance Renewable Sciences, Inc. METHODS OF MAKING α, ω -DICARBOXYLIC ACID ALKENE DERIVATIVES BY METATHESIS
US8501973B2 (en) 2006-10-13 2013-08-06 Elevance Renewable Sciences, Inc. Synthesis of terminal alkenes from internal alkenes via olefin metathesis
WO2008063322A2 (en) 2006-10-13 2008-05-29 Elevance Renewable Sciences, Inc. Metathesis methods involving hydrogenation and compositions relating to same
WO2008048520A2 (en) 2006-10-13 2008-04-24 Elevance Renewable Sciences, Inc. Methods of making organic compounds by metathesis and hydrocyanation
EP2183205A4 (en) * 2007-08-09 2013-10-02 Elevance Renewable Sciences CHEMICAL PROCESSES FOR TREATING METATHESIS RAW MATERIAL
FR2921363B1 (fr) * 2007-09-20 2009-11-06 Arkema France Procedes de synthese de diacides gras par metathese de diacides insatures obtenus par fermentation d'acides gras naturels
JP4594371B2 (ja) * 2007-11-30 2010-12-08 信越化学工業株式会社 (e3,z5)−3,5−アルカジエニルアセタートの製造方法
CN101502262B (zh) * 2009-03-20 2012-06-20 中国农业科学院草原研究所 草地螟性诱剂的合成及其应用
KR20120081120A (ko) * 2009-09-04 2012-07-18 유나이티드 파라곤 어소시에이츠 인크. 뉴로키닌 2 수용체 활성과 관련된 장애 또는 질환을 치료하기 위한 화합물
PL2488474T3 (pl) 2009-10-12 2017-07-31 Elevance Renewable Sciences, Inc. Sposoby rafinacji i wytwarzania paliw z surowców na bazie olejów naturalnych
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
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
US9175231B2 (en) 2009-10-12 2015-11-03 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
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
US9222056B2 (en) 2009-10-12 2015-12-29 Elevance Renewable Sciences, Inc. Methods of refining natural oils, and methods of producing fuel compositions
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
BR112013017900A2 (pt) * 2011-01-14 2016-07-12 Basf Se microcápsula, processo para a preparação de microcápsula, método e composição para o controle da infestação de insetos indesejáveis
US9150468B2 (en) 2011-09-28 2015-10-06 Nalco Company Method of producing olefins via metathesis
US9169174B2 (en) 2011-12-22 2015-10-27 Elevance Renewable Sciences, Inc. Methods for suppressing isomerization of olefin metathesis products
WO2013096413A2 (en) 2011-12-22 2013-06-27 Elevance Renewable Sciences, Inc. Methods for suppressing isomerization of olefin metathesis products, methods of refining natural oils, and methods of producing fuel compositions
US9133416B2 (en) 2011-12-22 2015-09-15 Elevance Renewable Sciences, Inc. Methods for suppressing isomerization of olefin metathesis products
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CN104508101A (zh) 2011-12-28 2015-04-08 艾勒旺斯可再生科学公司 可再生脂肪酸蜡及其制造方法
US20130331630A1 (en) * 2012-06-12 2013-12-12 Elevance Renewable Sciences, Inc. Methods for suppressing dehydrogenation
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EP2789602B1 (en) * 2013-04-12 2017-12-27 Shin-Etsu Chemical Co., Ltd Omega-halo-2-alkynal, method for producing the same, and method for producing conjugated Z-alken-yn-yl acetate using the same
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CN107406354B (zh) * 2015-03-03 2020-08-28 Agc株式会社 含氟烯烃化合物的制造方法
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PL3386936T3 (pl) * 2015-12-10 2024-10-07 Umicore Ag & Co. Kg Katalizatory metatezy olefin
CN105794775B (zh) * 2016-03-30 2018-05-08 中国检验检疫科学研究院 一种长小蠹科昆虫引诱剂及其制备方法与应用
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WO2018150379A2 (en) * 2017-02-17 2018-08-23 Provivi, Inc. Synthesis of pheromones and related materials via olefin metathesis
JP7023166B2 (ja) * 2018-04-18 2022-02-21 信越化学工業株式会社 (9e,11z)-9,11-ヘキサデカジエナールの製造方法
US12049443B2 (en) 2018-12-10 2024-07-30 Provivi, Inc. Synthesis of conjugated diene pheromones and related compounds
FR3098515B1 (fr) * 2019-07-12 2022-11-04 Melchior Material & Life Science France Nouvelles formulations stables de composés 1-Z-bromo alcènes-1 et leur utilisation dans la fabrication de phéromones
WO2021247583A1 (en) * 2020-06-01 2021-12-09 Provivi, Inc. Synthesis of pheromone derivatives via z-selective olefin metathesis
JP7291105B2 (ja) * 2020-06-24 2023-06-14 信越化学工業株式会社 (9z,11e)-9,11-ヘキサデカジエナールの製造方法
CN112782309B (zh) * 2020-12-29 2022-10-28 常州大学 一种稳定长链不饱和烯醛的方法
CN114507122B (zh) * 2022-01-28 2024-07-05 宜都市华阳化工有限责任公司 3-(4-甲基苯亚甲基)-樟脑合成副产物的回收利用方法
KR102473703B1 (ko) 2022-07-12 2022-12-01 전종열 사피엔산과 그 트랜스 이성질체 및 사피엔산 에스터를 제조하는 방법
CN115452991B (zh) * 2022-09-15 2024-07-12 江苏科技大学 十四碳烯酸和十六碳烯醛在检测检疫性害虫中的应用
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DE19907519A1 (de) * 1999-02-22 2000-08-31 Basf Ag Verfahren zur Herstellung von substituierten Olefinen
ATE248182T1 (de) * 1999-05-24 2003-09-15 California Inst Of Techn Imidazolidin enthaltende metallcarben- katalysatoren für die metathese

Also Published As

Publication number Publication date
ATE298318T1 (de) 2005-07-15
CA2392049C (en) 2012-01-31
IL149720A0 (en) 2002-11-10
BR0015712A (pt) 2004-04-27
JP5687114B2 (ja) 2015-03-18
JP2011178789A (ja) 2011-09-15
CN1423629A (zh) 2003-06-11
ZA200204712B (en) 2004-04-08
WO2001036368A2 (en) 2001-05-25
DE60020987T2 (de) 2006-05-11
CN100528829C (zh) 2009-08-19
DE60020987D1 (de) 2005-07-28
BR0015712B1 (pt) 2011-01-25
CA2392049A1 (en) 2001-05-25
JP2003531818A (ja) 2003-10-28
EP1230207A2 (en) 2002-08-14
WO2001036368A3 (en) 2002-01-10
EP1230207B1 (en) 2005-06-22
JP4943612B2 (ja) 2012-05-30
IL149720A (en) 2008-03-20

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