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 PDFInfo
- Publication number
- 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
- Authority
- CN
- China
- Prior art keywords
- formula
- compound
- dimethoxyphenyl
- trans
- definition
- 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.)
- Expired - Fee Related
Links
- 0 CC(*)=CC(O*)=CC(C=C[C@]1C=C(*)C(O*)=CC1)=C Chemical compound CC(*)=CC(O*)=CC(C=C[C@]1C=C(*)C(O*)=CC1)=C 0.000 description 3
Images
Classifications
-
- 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
Landscapes
- 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)
Abstract
Description
Claims (28)
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR06/53178 | 2006-07-28 | ||
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 |
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 |
Family
ID=37864505
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
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 (zh) |
EP (2) | EP2049459B8 (zh) |
JP (1) | JP5254974B2 (zh) |
CN (1) | CN101495436B (zh) |
CA (1) | CA2658652C (zh) |
ES (2) | ES2436034T3 (zh) |
FR (1) | FR2904311B1 (zh) |
RU (1) | RU2443671C2 (zh) |
WO (1) | WO2008012321A1 (zh) |
Families Citing this family (13)
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 |
CN101284755B (zh) * | 2008-05-19 | 2011-07-27 | 浙江工业大学 | 共轭烯烃类化合物的化学合成方法 |
KR101048475B1 (ko) | 2008-12-03 | 2011-07-11 | 전남대학교산학협력단 | 박테리아 사이토크롬 피450을 이용한 피세아타놀의 신규한 생산방법 및 이를 위한 조성물 |
EP2724156B1 (en) | 2011-06-27 | 2017-08-16 | The Jackson Laboratory | Methods and compositions for treatment of cancer and autoimmune disease |
CN103172512B (zh) * | 2011-12-23 | 2016-08-03 | 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、制备方法和应用 |
WO2014127171A1 (en) * | 2013-02-13 | 2014-08-21 | Indiana University Research And Technology Corporation | Poly-cyanostilbene macrocycles |
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 |
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)
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 |
WO2000015603A1 (fr) * | 1998-09-11 | 2000-03-23 | Ajinomoto Co., Inc. | Derives de benzene et leur utilisation medicale |
FR2789577B1 (fr) * | 1999-02-17 | 2002-04-05 | Oreal | Utilisation de derives substitues en 3 du stilbene comme actifs deodorants dans les compositions cosmetiques |
CA2373603A1 (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 |
US7820848B2 (en) * | 2003-09-05 | 2010-10-26 | Dsm Ip Assets B.V. | Process for the preparation of stilbene derivatives |
WO2005069998A2 (en) | 2004-01-20 | 2005-08-04 | Brigham Young University Technology Transfer Office | Novel sirtuin activating compounds and methods for making the same |
EP1884508A1 (en) | 2006-07-28 | 2008-02-06 | Portela & Ca., S.A. | Process for the preparation of polyhydroxylated stilbenes via claisen condensation |
WO2008012108A2 (en) * | 2006-07-28 | 2008-01-31 | Portela & Ca., S.A. | Process for the preparation of polyhydroxylated stilbenes via claisen condensation |
-
2006
- 2006-07-28 FR FR0653178A patent/FR2904311B1/fr not_active Expired - Fee Related
-
2007
- 2007-07-25 ES ES09015839T patent/ES2436034T3/es active Active
- 2007-07-25 ES ES07787880T patent/ES2436110T3/es active Active
- 2007-07-25 CN CN200780027871.0A patent/CN101495436B/zh not_active Expired - Fee Related
- 2007-07-25 CA CA2658652A patent/CA2658652C/en not_active Expired - Fee Related
- 2007-07-25 RU RU2009107169/04A patent/RU2443671C2/ru not_active IP Right Cessation
- 2007-07-25 JP JP2009521253A patent/JP5254974B2/ja not_active Expired - Fee Related
- 2007-07-25 WO PCT/EP2007/057650 patent/WO2008012321A1/en active Application Filing
- 2007-07-25 EP EP07787880.9A patent/EP2049459B8/en not_active Not-in-force
- 2007-07-25 US US12/375,507 patent/US8101804B2/en not_active Expired - Fee Related
- 2007-07-25 EP EP09015839.5A patent/EP2202215B8/en not_active Not-in-force
Also Published As
Publication number | Publication date |
---|---|
CN101495436A (zh) | 2009-07-29 |
EP2202215A2 (en) | 2010-06-30 |
JP2009544663A (ja) | 2009-12-17 |
US20100004483A1 (en) | 2010-01-07 |
FR2904311A1 (fr) | 2008-02-01 |
EP2202215B1 (en) | 2013-10-02 |
JP5254974B2 (ja) | 2013-08-07 |
EP2049459B8 (en) | 2013-11-13 |
ES2436110T3 (es) | 2013-12-27 |
EP2049459A1 (en) | 2009-04-22 |
WO2008012321A1 (en) | 2008-01-31 |
CA2658652C (en) | 2014-10-28 |
ES2436034T3 (es) | 2013-12-26 |
EP2202215B8 (en) | 2013-11-13 |
CA2658652A1 (en) | 2008-01-31 |
RU2443671C2 (ru) | 2012-02-27 |
FR2904311B1 (fr) | 2013-01-11 |
EP2202215A3 (en) | 2010-09-08 |
EP2049459B1 (en) | 2013-10-02 |
RU2009107169A (ru) | 2010-09-10 |
US8101804B2 (en) | 2012-01-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101495436B (zh) | 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 | |
Soula | Tris (polyoxaalkyl) amines (trident), a new class of solid-liquid phase-transfer catalysts | |
US9085519B2 (en) | Processes for producing benzophenone derivatives | |
JPS6333424B2 (zh) | ||
WO2001060774A1 (en) | Synthesis of resveratrol | |
EP0273528A1 (en) | Benzophenones and their preparation | |
Tangdenpaisal et al. | Factors affecting orthogonality in the deprotection of 2, 4-di-protected aromatic ethers employing solid-supported acids | |
US8212081B2 (en) | Process for preparing substituted 1,4-quinone methides | |
Lopušanskaja et al. | Towards ortho-selective electrophilic substitution/addition to phenolates in anhydrous solvents | |
CA2311064A1 (en) | Substituted tetraarylethylene compounds | |
Liu et al. | Cobalt/Lewis acid cooperative catalysis for reductive etherification of ketones and aldehydes with alcohols | |
JPS60215636A (ja) | フエノール類の選択的c‐アルキル化方法 | |
US4087410A (en) | 5-(Tertiary alkyl) resorcinol preparation and intermediates therefor | |
KR20040055817A (ko) | 3,3',6,6'-테트라알킬-2,2'-비페놀 및3,3',6,6'-테트라알킬-5,5'-디할로-2,2'-비페놀의 제조방법 | |
HU208533B (en) | Process for selective etherification of ascorbinic acid derivatives | |
Murphy et al. | Intramolecular alkylation of phenols. Part 5. A regiospecific anionic ring closure of phenols via quinone methides | |
CN101977883A (zh) | 2-羟基芳基醛化合物的制造方法 | |
Ahmad et al. | Borontribromide-mediated C–C bond formation in cyclic ketones: a transition metal free approach | |
Azzena et al. | Ion pairing effects on the regioselectivity of arylic versus benzylic C–O bond reductive cleavage: synthetic applications | |
EP2452938A1 (en) | Process for the preparation of 3-aroyl-5-aminobenzofuran derivatives | |
JP4643842B2 (ja) | 3,5−ビスアルキルフェノールの製造法 | |
RU2100341C1 (ru) | 4-метоксиалкил-2-трет.бутилфенолы в качестве промежуточных соединений в синтезе метопролола и его аналогов | |
Kasák et al. | (R, R, R)-Tris (2-hydroxy-1-methylethyl)-and (S, S, S)-tris (2-hydroxy-2-methylethyl) phosphine: water-soluble chiral trialkylphosphines with C3-symmetry | |
WO2022099930A1 (zh) | 一种大麻黄酮类化合物的制备方法 | |
CN117342931A (zh) | 一种5-烷基间苯二酚类化合物的制备方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C53 | Correction of patent of invention or patent application | ||
CB02 | Change of applicant information |
Address after: French Te Rosli Buller I Applicant after: Clariant Specialty Fine Chemicals (France) Address before: French pitot Applicant before: Clariant Specialty Fine Chemicals (France) |
|
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
C56 | Change in the name or address of the patentee |
Owner name: CLARIANT CHEMICAL LAMOTTE SIMPLIFIED CORPORATION Free format text: FORMER NAME: CLARIANT SPECIALTY FINE CHEMIC |
|
CP03 | Change of name, title or address |
Address after: Union of France Patentee after: Simple chemical Co.,Ltd. for Maxwell Address before: French Te Rosli Buller I Patentee before: Clariant Specialty Fine Chemicals (France) |
|
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20140226 |
|
CF01 | Termination of patent right due to non-payment of annual fee |