CN101495436B - 可以得到白藜芦醇和四羟反式茋的合成(e)-茋衍生物的方法 - Google Patents

可以得到白藜芦醇和四羟反式茋的合成(e)-茋衍生物的方法 Download PDF

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CN101495436B
CN101495436B CN200780027871.0A CN200780027871A CN101495436B CN 101495436 B CN101495436 B CN 101495436B CN 200780027871 A CN200780027871 A CN 200780027871A CN 101495436 B CN101495436 B CN 101495436B
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formula
compound
dimethoxyphenyl
group
vii
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Chinese (zh)
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CN101495436A (zh
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A·肖蒂滕
S·朱斯
J·-C·瓦莱约斯
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Simple Chemical Co ltd For Maxwell
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Clariant Speciality Fine Chemicals France
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/48—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups having nitrogen atoms of sulfonamide groups further bound to another hetero atom
    • C07C311/49—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups having nitrogen atoms of sulfonamide groups further bound to another hetero atom to nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C303/00—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides
    • C07C303/36—Preparation of esters or amides of sulfuric acids; Preparation of sulfonic acids or of their esters, halides, anhydrides or amides of amides of sulfonic acids
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C37/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
    • C07C37/01—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis
    • C07C37/055—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by replacing functional groups bound to a six-membered aromatic ring by hydroxy groups, e.g. by hydrolysis the substituted group being bound to oxygen, e.g. ether group
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01—Preparation of ethers
    • C07C41/18—Preparation of ethers by reactions not forming ether-oxygen bonds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01—Preparation of ethers
    • C07C41/18—Preparation of ethers by reactions not forming ether-oxygen bonds
    • C07C41/26—Preparation of ethers by reactions not forming ether-oxygen bonds by introduction of hydroxy or O-metal groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C43/00—Ethers; Compounds having groups, groups or groups
    • C07C43/02—Ethers
    • C07C43/20—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring
    • C07C43/23—Ethers having an ether-oxygen atom bound to a carbon atom of a six-membered aromatic ring containing hydroxy or O-metal groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
    • C07C45/673—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by change of size of the carbon skeleton
    • C07C45/676—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by change of size of the carbon skeleton by elimination of carboxyl groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/30—Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/333—Preparation 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
    • C07C67/343—Preparation 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/66—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety
    • C07C69/73—Esters of carboxylic acids having esterified carboxylic groups bound to acyclic carbon atoms and having any of the groups OH, O—metal, —CHO, keto, ether, acyloxy, groups, groups, or in the acid moiety of unsaturated acids
    • C07C69/738—Esters of keto-carboxylic acids or aldehydo-carboxylic acids

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
CN200780027871.0A 2006-07-28 2007-07-25 可以得到白藜芦醇和四羟反式茋的合成(e)-茋衍生物的方法 Expired - Fee Related CN101495436B (zh)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR0653178A FR2904311B1 (fr) 2006-07-28 2006-07-28 Nouveau procede de synthese de derives (e) stilbeniques perm permettant d'obtenir le resveratrol et le piceatannol
FR06/53178 2006-07-28
PCT/EP2007/057650 WO2008012321A1 (en) 2006-07-28 2007-07-25 Novel process for the synthesis of (e)-stilbene derivatives which makes it possible to obtain resveratrol and piceatannol

Publications (2)

Publication Number Publication Date
CN101495436A CN101495436A (zh) 2009-07-29
CN101495436B true CN101495436B (zh) 2014-02-26

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CN200780027871.0A Expired - Fee Related CN101495436B (zh) 2006-07-28 2007-07-25 可以得到白藜芦醇和四羟反式茋的合成(e)-茋衍生物的方法

Country Status (9)

Country Link
US (1) US8101804B2 (https=)
EP (2) EP2202215B8 (https=)
JP (1) JP5254974B2 (https=)
CN (1) CN101495436B (https=)
CA (1) CA2658652C (https=)
ES (2) ES2436110T3 (https=)
FR (1) FR2904311B1 (https=)
RU (1) RU2443671C2 (https=)
WO (1) WO2008012321A1 (https=)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2921921B1 (fr) * 2007-10-03 2011-08-19 Clariant Specialty Fine Chem F Procede de synthese de composes polyhydroxystilbeniques.
CN101139267B (zh) * 2007-10-09 2014-01-29 沈阳药科大学 白藜芦醇衍生物、类似物及其制备方法和用途
KR101048475B1 (ko) 2008-12-03 2011-07-11 전남대학교산학협력단 박테리아 사이토크롬 피450을 이용한 피세아타놀의 신규한 생산방법 및 이를 위한 조성물
AU2012275841A1 (en) 2011-06-27 2014-01-16 The Jackson Laboratory Methods and compositions for treatment of cancer and autoimmune disease
CN105030750B (zh) * 2011-12-23 2018-08-28 中国医学科学院医药生物技术研究所 一组木豆素结构类似化合物在抗丙肝病毒和抗艾滋病毒的应用
US10077233B2 (en) 2013-02-13 2018-09-18 Indiana University Research And Technology Corporation Poly-cyanostilbene macrocycles
US9701621B2 (en) 2013-02-13 2017-07-11 Indiana University Research & Technology Corporation Poly-cyanostilbene macrocycles
WO2014127171A1 (en) * 2013-02-13 2014-08-21 Indiana University Research And Technology Corporation Poly-cyanostilbene macrocycles
US8921614B1 (en) * 2013-02-26 2014-12-30 The United States Of America As Represented By The Secretary Of The Navy Selective deoxygenation of hydroxybenzaldehydes
CN103992290B (zh) * 2013-05-14 2016-07-06 中国医学科学院医药生物技术研究所 二芳基乙烯结构类似化合物及其制备方法和应用
TW201702218A (zh) 2014-12-12 2017-01-16 美國杰克森實驗室 關於治療癌症、自體免疫疾病及神經退化性疾病之組合物及方法
FR3029912B1 (fr) * 2014-12-12 2018-03-09 L'oreal Nouveaux derives de resveratrol pour lutter contre le vieillissement cutane, compositions et utilisation en cosmetique

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2537950A (en) * 1948-11-05 1951-01-16 Milton J Allen Preparation of substituted diamino-stilbenes from pinacols
US3767289A (en) * 1970-12-31 1973-10-23 Ibm Class of stable trans-stilbene compounds, some displaying nematic mesophases at or near room temperature and others in a range up to 100{20 {11 c
JP3330155B2 (ja) * 1991-02-22 2002-09-30 石原産業株式会社 ヒドラゾン系化合物、それらの製造方法及びそれらの製造用中間体ならびにそれらを含有する有害生物防除剤
KR20010079782A (ko) * 1998-09-11 2001-08-22 에가시라 구니오 벤젠 유도체 및 이의 의약 용도
FR2789577B1 (fr) * 1999-02-17 2002-04-05 Oreal Utilisation de derives substitues en 3 du stilbene comme actifs deodorants dans les compositions cosmetiques
WO2000069430A1 (en) 1999-05-18 2000-11-23 Calyx Therapeutics, Inc. Novel diphenylethylene compounds
WO2001060774A1 (en) * 2000-02-16 2001-08-23 Brigham Young University Synthesis of resveratrol
WO2003086414A1 (en) * 2002-04-10 2003-10-23 Arizona Board Of Regents Structural modification of resveratrol: sodium resverastatin phosphate
EP1466884A1 (fr) 2003-04-08 2004-10-13 Sochinaz SA Procédé de préparation du resvératrol et ses applications
CN100348564C (zh) * 2003-09-05 2007-11-14 帝斯曼知识产权资产管理有限公司 二苯乙烯衍生物的制备方法
US7714161B2 (en) 2004-01-20 2010-05-11 Brigham Young University Sirtuin activating compounds and methods for making the same
WO2008012108A2 (en) * 2006-07-28 2008-01-31 Portela & Ca., S.A. Process for the preparation of polyhydroxylated stilbenes via claisen condensation
EP1884508A1 (en) 2006-07-28 2008-02-06 Portela & Ca., S.A. Process for the preparation of polyhydroxylated stilbenes via claisen condensation

Also Published As

Publication number Publication date
ES2436110T3 (es) 2013-12-27
US8101804B2 (en) 2012-01-24
FR2904311B1 (fr) 2013-01-11
EP2202215B1 (en) 2013-10-02
EP2202215A2 (en) 2010-06-30
JP5254974B2 (ja) 2013-08-07
CA2658652A1 (en) 2008-01-31
FR2904311A1 (fr) 2008-02-01
EP2049459A1 (en) 2009-04-22
CA2658652C (en) 2014-10-28
EP2202215A3 (en) 2010-09-08
JP2009544663A (ja) 2009-12-17
EP2202215B8 (en) 2013-11-13
US20100004483A1 (en) 2010-01-07
RU2443671C2 (ru) 2012-02-27
WO2008012321A1 (en) 2008-01-31
EP2049459B1 (en) 2013-10-02
ES2436034T3 (es) 2013-12-26
EP2049459B8 (en) 2013-11-13
RU2009107169A (ru) 2010-09-10
CN101495436A (zh) 2009-07-29

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Address after: French Te Rosli Buller I

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Owner name: CLARIANT CHEMICAL LAMOTTE SIMPLIFIED CORPORATION

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Patentee after: Simple chemical Co.,Ltd. for Maxwell

Address before: French Te Rosli Buller I

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Granted publication date: 20140226