BR0015712B1 - sìntese de metátese de feromÈnios ou seus componentes. - Google Patents

sìntese de metátese de feromÈnios ou seus componentes.

Info

Publication number
BR0015712B1
BR0015712B1 BRPI0015712-0A BR0015712A BR0015712B1 BR 0015712 B1 BR0015712 B1 BR 0015712B1 BR 0015712 A BR0015712 A BR 0015712A BR 0015712 B1 BR0015712 B1 BR 0015712B1
Authority
BR
Brazil
Prior art keywords
pheromone
omega
syntheses
acetate
metathesis
Prior art date
Application number
BRPI0015712-0A
Other languages
English (en)
Portuguese (pt)
Other versions
BR0015712A (pt
Inventor
Richard L Pederson
Robert H Grubbs
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 filed Critical
Publication of BR0015712A publication Critical patent/BR0015712A/pt
Publication of BR0015712B1 publication Critical patent/BR0015712B1/pt

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)
BRPI0015712-0A 1999-11-18 2000-11-17 sìntese de metátese de feromÈnios ou seus componentes. BR0015712B1 (pt)

Applications Claiming Priority (2)

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

Publications (2)

Publication Number Publication Date
BR0015712A BR0015712A (pt) 2004-04-27
BR0015712B1 true BR0015712B1 (pt) 2011-01-25

Family

ID=22603759

Family Applications (1)

Application Number Title Priority Date Filing Date
BRPI0015712-0A BR0015712B1 (pt) 1999-11-18 2000-11-17 sìntese de metátese de feromÈnios ou seus componentes.

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)

Families Citing this family (57)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002020395A (ja) * 2000-07-04 2002-01-23 Sekisui Chem Co Ltd 新規な高メタセシス活性の有機金属錯体化合物、これを含有してなるメタセシス反応触媒、この触媒を用いた重合方法、並びにこの重合方法により得られた樹脂組成物
WO2002079126A1 (en) 2001-03-30 2002-10-10 California Institute Of Technology Cross-metathesis reaction of functionalized and substituted olefins using group 8 transition metal carbene complexes as metathesis catalysts
BRPI0406756A (pt) 2003-01-13 2005-12-20 Cargill Inc Método para fabricação de agentes quìmicos industriais
BRPI0606718A2 (pt) 2005-01-10 2009-07-14 Cargill Inc vela e cera para vela contendo produtos de metátese e semelhantes a metátese
KR101269568B1 (ko) * 2005-07-04 2013-06-04 자난 사이텍 컴퍼니 리미티드 루테늄 착물 리간드, 루테늄 착물, 고정 루테늄 착물 촉매및 그의 제조방법과 용도
WO2007081987A2 (en) * 2006-01-10 2007-07-19 Elevance Renewable Sciences, Inc. Method of making hydrogenated metathesis products
US8888908B2 (en) 2006-03-07 2014-11-18 Elevance Renewable Sciences, Inc. Colorant compositions comprising metathesized unsaturated polyol esters
CN102525829B (zh) 2006-03-07 2014-08-06 埃莱文斯可更新科学公司 含有复分解不饱和多元醇酯的组合物
EP2046908B1 (en) 2006-07-12 2017-01-11 Elevance Renewable Sciences, Inc. Hot melt adhesive compositions comprising metathesized unsaturated polyol ester wax
WO2008010961A2 (en) 2006-07-13 2008-01-24 Elevance Renewable Sciences, Inc. 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
CN106083579A (zh) 2006-10-13 2016-11-09 埃莱文斯可更新科学公司 通过烯烃复分解由内烯烃合成末端烯烃的方法
WO2008048520A2 (en) 2006-10-13 2008-04-24 Elevance Renewable Sciences, Inc. Methods of making organic compounds by metathesis and hydrocyanation
DK2121546T3 (en) 2006-10-13 2018-03-12 Elevance Renewable Sciences Process for preparing omega-dicarboxylic acid olefin derivative by metathesis
ATE519725T1 (de) 2006-10-13 2011-08-15 Elevance Renewable Sciences Metatheseverfahren mit hydrierung, und damit in zusammenhang stehende zusammensetzungen
BRPI0814994A2 (pt) * 2007-08-09 2015-02-03 Elevance Renewable Sciences Métodos químicos para tratamento de uma matéria-prima de metátese
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
EP2473038A4 (en) * 2009-09-04 2013-10-23 United Paragon Associates Inc COMPOSITIONS FOR TREATING SUFFICIENT OR ILLNESSES PROVIDED BY NEUROKININ-2-RECEPTOR ACTIVITY
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
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
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
US9051519B2 (en) 2009-10-12 2015-06-09 Elevance Renewable Sciences, Inc. Diene-selective hydrogenation of metathesis derived olefins and unsaturated esters
US9169447B2 (en) 2009-10-12 2015-10-27 Elevance Renewable Sciences, Inc. Methods of refining natural oils, and methods of producing fuel compositions
US9222056B2 (en) 2009-10-12 2015-12-29 Elevance Renewable Sciences, Inc. Methods of refining natural oils, and methods of producing fuel compositions
US8957268B2 (en) 2009-10-12 2015-02-17 Elevance Renewable Sciences, Inc. Methods of refining natural oil feedstocks
ES2608556T3 (es) * 2011-01-14 2017-04-12 Basf Se Composición atrayente que contiene etil 3-metilbutanoato y (E,E)-8-,10-dodecadien-1-ol
US9150468B2 (en) * 2011-09-28 2015-10-06 Nalco Company Method of producing olefins via metathesis
US9133416B2 (en) 2011-12-22 2015-09-15 Elevance Renewable Sciences, Inc. Methods for suppressing isomerization of olefin metathesis products
MX348233B (es) 2011-12-22 2017-05-30 Elevance Renewable Sciences Metodos para suprimir la isomerizacion de productos de metatesis de olefina, metodos de refinación de aceites naturales, y metodos de producción de composiciones de combustible.
US9139493B2 (en) 2011-12-22 2015-09-22 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
EP2804936B1 (en) 2012-01-10 2016-03-23 Elevance Renewable Sciences, Inc. Renewable fatty acid waxes and methods of making
EP2859068A1 (en) * 2012-06-12 2015-04-15 Elevance Renewable Sciences, Inc. Methods for suppressing dehydrogenation
EP2864447B3 (en) 2012-06-20 2019-07-17 Elevance Renewable Sciences, Inc. Natural oil metathesis compositions
US9388098B2 (en) 2012-10-09 2016-07-12 Elevance Renewable Sciences, Inc. Methods of making high-weight esters, acids, and derivatives thereof
ES2662827T3 (es) * 2013-04-12 2018-04-09 Shin-Etsu Chemical Co., Ltd Omega-halo-2-alquinal, procedimiento de producción del mismo y procedimiento de producción de acetato de Z-alquen-in-ilo conjugado usando el mismo
GB201404468D0 (en) 2014-03-13 2014-04-30 Givaudan Sa Process
JP6572966B2 (ja) * 2015-03-03 2019-09-11 Agc株式会社 含フッ素オレフィン化合物の製造方法
AU2016357756B2 (en) * 2015-11-18 2021-09-30 Provivi, Inc. Production of fatty olefin derivatives via olefin metathesis
WO2017100585A1 (en) * 2015-12-10 2017-06-15 Materia, Inc. Olefin metathesis catalysts
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
WO2018069146A1 (fr) 2016-10-11 2018-04-19 Demeta Procede de synthese de pheromones
CN110603240B (zh) * 2017-02-17 2022-11-15 普罗维维公司 通过烯烃复分解合成信息素和相关物质
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
WO2020123534A1 (en) 2018-12-10 2020-06-18 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
CN117682940A (zh) * 2023-11-13 2024-03-12 中捷四方生物科技股份有限公司 无患子在制备昆虫信息素中的应用

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2196061C (en) * 1992-04-03 2000-06-13 Robert H. Grubbs High activity ruthenium or osmium metal carbene complexes for olefin metathesis reactions and synthesis thereof
US5916983A (en) * 1997-05-27 1999-06-29 Bend Research, Inc. Biologically active compounds by catalytic olefin metathesis
JP3942122B2 (ja) * 1997-12-26 2007-07-11 高砂香料工業株式会社 ルテニウムメタセシス触媒およびそれを用いたメタセ シス反応によるオレフィン反応生成物を製造する方法
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
JP2002535297A (ja) * 1999-01-26 2002-10-22 カリフォルニア インスティチュート オブ テクノロジー 末端オレフィンのクロスメタセシスのための方法
DE19907519A1 (de) * 1999-02-22 2000-08-31 Basf Ag Verfahren zur Herstellung von substituierten Olefinen
JP4410422B2 (ja) * 1999-05-24 2010-02-03 カリフォルニア インスティチュート オブ テクノロジー イミダゾリジンに基づく金属カルベンメタセシス触媒

Also Published As

Publication number Publication date
CN1423629A (zh) 2003-06-11
ZA200204712B (en) 2004-04-08
BR0015712A (pt) 2004-04-27
JP2003531818A (ja) 2003-10-28
CN100528829C (zh) 2009-08-19
ATE298318T1 (de) 2005-07-15
JP2011178789A (ja) 2011-09-15
EP1230207A2 (en) 2002-08-14
JP5687114B2 (ja) 2015-03-18
CA2392049C (en) 2012-01-31
JP4943612B2 (ja) 2012-05-30
DE60020987D1 (de) 2005-07-28
IL149720A (en) 2008-03-20
EP1230207B1 (en) 2005-06-22
IL149720A0 (en) 2002-11-10
DE60020987T2 (de) 2006-05-11
WO2001036368A3 (en) 2002-01-10
AU1921201A (en) 2001-05-30
WO2001036368A2 (en) 2001-05-25
CA2392049A1 (en) 2001-05-25

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