CN101952298B - 用于过渡金属催化的交联偶合反应的配体及其使用方法 - Google Patents
用于过渡金属催化的交联偶合反应的配体及其使用方法 Download PDFInfo
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- CN101952298B CN101952298B CN200880126921.5A CN200880126921A CN101952298B CN 101952298 B CN101952298 B CN 101952298B CN 200880126921 A CN200880126921 A CN 200880126921A CN 101952298 B CN101952298 B CN 101952298B
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- 0 CCCCC1C(C*2=C(C)CCC2C)C1 Chemical compound CCCCC1C(C*2=C(C)CCC2C)C1 0.000 description 17
- KWHPWBXOLZTZMJ-UHFFFAOYSA-N CCC1CCNCC1 Chemical compound CCC1CCNCC1 KWHPWBXOLZTZMJ-UHFFFAOYSA-N 0.000 description 2
- UMNSMBWAESLVOC-UHFFFAOYSA-N CCCCCNc1ccccc1 Chemical compound CCCCCNc1ccccc1 UMNSMBWAESLVOC-UHFFFAOYSA-N 0.000 description 2
- WGUXTQDCAZNJIF-UHFFFAOYSA-N Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1 Chemical compound Cc1cc(C(F)(F)F)cc(C(F)(F)F)c1 WGUXTQDCAZNJIF-UHFFFAOYSA-N 0.000 description 2
- LRLRAYMYEXQKID-UHFFFAOYSA-N Cc1ccc(C(F)(F)F)cc1 Chemical compound Cc1ccc(C(F)(F)F)cc1 LRLRAYMYEXQKID-UHFFFAOYSA-N 0.000 description 2
- LFMFOONRIUTFFG-UHFFFAOYSA-N CCC(C)C1C(c(c(I)c(cc2)O)c2OC)=C(C(C)CC)C=C(Cc2ccccc2)C1 Chemical compound CCC(C)C1C(c(c(I)c(cc2)O)c2OC)=C(C(C)CC)C=C(Cc2ccccc2)C1 LFMFOONRIUTFFG-UHFFFAOYSA-N 0.000 description 1
- RVTQZBXFKNQBAM-UHFFFAOYSA-N CCOC(c(cc1)ccc1Nc1ccccc1OC)=O Chemical compound CCOC(c(cc1)ccc1Nc1ccccc1OC)=O RVTQZBXFKNQBAM-UHFFFAOYSA-N 0.000 description 1
- VONUJCUIZJOVGS-UHFFFAOYSA-N CCOC(c(cccc1)c1Nc(cc1)ccc1F)=O Chemical compound CCOC(c(cccc1)c1Nc(cc1)ccc1F)=O VONUJCUIZJOVGS-UHFFFAOYSA-N 0.000 description 1
- WSJNYOVBJSOQST-UHFFFAOYSA-N CCOC(c1cccc(C)c1)=O Chemical compound CCOC(c1cccc(C)c1)=O WSJNYOVBJSOQST-UHFFFAOYSA-N 0.000 description 1
- WNCYZVMZKSOPMU-UHFFFAOYSA-N COc(cc1F)ccc1OC Chemical compound COc(cc1F)ccc1OC WNCYZVMZKSOPMU-UHFFFAOYSA-N 0.000 description 1
- RLBMOECAVLNERB-UHFFFAOYSA-N COc1cc(Nc(cc2)ccc2F)cc(OC)c1OC Chemical compound COc1cc(Nc(cc2)ccc2F)cc(OC)c1OC RLBMOECAVLNERB-UHFFFAOYSA-N 0.000 description 1
- DPZNOMCNRMUKPS-UHFFFAOYSA-N COc1cc(OC)ccc1 Chemical compound COc1cc(OC)ccc1 DPZNOMCNRMUKPS-UHFFFAOYSA-N 0.000 description 1
- HKGGLGPUDBAOBI-UHFFFAOYSA-N C[N](C)(Cc1c(cc2)OC)c3ccccc3-c1c2OC Chemical compound C[N](C)(Cc1c(cc2)OC)c3ccccc3-c1c2OC HKGGLGPUDBAOBI-UHFFFAOYSA-N 0.000 description 1
- LUYISICIYVKBTA-UHFFFAOYSA-N Cc(cc1)cc2c1nccc2 Chemical compound Cc(cc1)cc2c1nccc2 LUYISICIYVKBTA-UHFFFAOYSA-N 0.000 description 1
- ZZLCFHIKESPLTH-UHFFFAOYSA-N Cc(cc1)ccc1-c1ccccc1 Chemical compound Cc(cc1)ccc1-c1ccccc1 ZZLCFHIKESPLTH-UHFFFAOYSA-N 0.000 description 1
- WRWPPGUCZBJXKX-UHFFFAOYSA-N Cc(cc1)ccc1F Chemical compound Cc(cc1)ccc1F WRWPPGUCZBJXKX-UHFFFAOYSA-N 0.000 description 1
- CHLICZRVGGXEOD-UHFFFAOYSA-N Cc(cc1)ccc1OC Chemical compound Cc(cc1)ccc1OC CHLICZRVGGXEOD-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N Cc1c(C)cccc1 Chemical compound Cc1c(C)cccc1 CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- GWHJZXXIDMPWGX-UHFFFAOYSA-N Cc1ccc(C)c(C)c1 Chemical compound Cc1ccc(C)c(C)c1 GWHJZXXIDMPWGX-UHFFFAOYSA-N 0.000 description 1
- YXFVVABEGXRONW-UHFFFAOYSA-N Cc1ccccc1 Chemical compound Cc1ccccc1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 1
- BSKHPKMHTQYZBB-UHFFFAOYSA-N Cc1ccccn1 Chemical compound Cc1ccccn1 BSKHPKMHTQYZBB-UHFFFAOYSA-N 0.000 description 1
- ITQTTZVARXURQS-UHFFFAOYSA-N Cc1cnccc1 Chemical compound Cc1cnccc1 ITQTTZVARXURQS-UHFFFAOYSA-N 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/50—Organo-phosphines
- C07F9/5022—Aromatic phosphines (P-C aromatic linkage)
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C209/00—Preparation of compounds containing amino groups bound to a carbon skeleton
- C07C209/04—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups
- C07C209/06—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of halogen atoms
- C07C209/10—Preparation of compounds containing amino groups bound to a carbon skeleton by substitution of functional groups by amino groups by substitution of halogen atoms with formation of amino groups bound to carbon atoms of six-membered aromatic rings or from amines having nitrogen atoms bound to carbon atoms of six-membered aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C213/00—Preparation of compounds containing amino and hydroxy, amino and etherified hydroxy or amino and esterified hydroxy groups bound to the same carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C231/00—Preparation of carboxylic acid amides
- C07C231/08—Preparation of carboxylic acid amides from amides by reaction at nitrogen atoms of carboxamide groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
- C07D241/02—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings
- C07D241/10—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D241/14—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D241/20—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
- C07F15/006—Palladium compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
- Catalysts (AREA)
- Quinoline Compounds (AREA)
- Pyridine Compounds (AREA)
- Pyrrole Compounds (AREA)
- Hydrogenated Pyridines (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US1317407P | 2007-12-12 | 2007-12-12 | |
| US61/013174 | 2007-12-12 | ||
| US8736808P | 2008-08-08 | 2008-08-08 | |
| US61/087368 | 2008-08-08 | ||
| PCT/US2008/086651 WO2009076622A2 (en) | 2007-12-12 | 2008-12-12 | Ligands for transition-metal-catalyzed cross-couplings, and methods of use thereof |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN101952298A CN101952298A (zh) | 2011-01-19 |
| CN101952298B true CN101952298B (zh) | 2015-06-17 |
Family
ID=40756138
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN200880126921.5A Active CN101952298B (zh) | 2007-12-12 | 2008-12-12 | 用于过渡金属催化的交联偶合反应的配体及其使用方法 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7858784B2 (OSRAM) |
| EP (1) | EP2231680B1 (OSRAM) |
| JP (1) | JP5591714B2 (OSRAM) |
| CN (1) | CN101952298B (OSRAM) |
| CA (1) | CA2708369C (OSRAM) |
| WO (1) | WO2009076622A2 (OSRAM) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2556077B1 (en) * | 2010-04-05 | 2014-03-19 | Boehringer Ingelheim International GmbH | Monophosphorus ligands and their use in cross-coupling reactions |
| CR20180412A (es) | 2010-07-16 | 2018-11-01 | Abbvie Ireland Unlimited Co | Proceso para preparar compuestos antivirales |
| US8975443B2 (en) | 2010-07-16 | 2015-03-10 | Abbvie Inc. | Phosphine ligands for catalytic reactions |
| US8841487B2 (en) | 2010-07-16 | 2014-09-23 | Abbvie Inc. | Phosphine ligands for catalytic reactions |
| US9255074B2 (en) | 2010-07-16 | 2016-02-09 | Abbvie Inc. | Process for preparing antiviral compounds |
| CN102241614B (zh) * | 2011-05-10 | 2015-09-02 | 浙江建业化工股份有限公司 | 一种n-烃基取代酰胺化合物的合成方法 |
| CN102516300A (zh) * | 2011-11-09 | 2012-06-27 | 中山大学 | 一类膦配体及其对映体或消旋体及其制备方法 |
| CN102557966A (zh) * | 2011-12-23 | 2012-07-11 | 中国石油化工股份有限公司 | 一种制备防老剂dtpd的方法 |
| WO2013159229A1 (en) * | 2012-04-24 | 2013-10-31 | Dalhousie University | Silanyloxyaryl phosphine ligand and uses thereof in c-n cross-coupling |
| EP2859005B1 (en) | 2012-06-08 | 2018-10-31 | Massachusetts Institute of Technology | Phosphine-ligated palladium sulfonate palladacycles |
| US9238665B2 (en) * | 2012-07-06 | 2016-01-19 | Sumitomo Chemical Company, Limited | Method for producing aromatic compound |
| CN110003271B (zh) | 2012-07-06 | 2022-05-03 | 住友化学株式会社 | 芳香族化合物的制备方法 |
| EP2900657B1 (en) | 2012-09-26 | 2020-03-11 | F.Hoffmann-La Roche Ag | Cyclic ether pyrazol-4-yl-heterocyclyl-carboxamide compounds and methods of use |
| JP6123097B2 (ja) | 2012-10-10 | 2017-05-10 | エフ・ホフマン−ラ・ロシュ・アクチェンゲゼルシャフト | チエノピリミジン化合物を製造するための方法 |
| EP2920144A4 (en) * | 2012-11-15 | 2016-06-29 | Univ Holy Ghost Duquesne | CARBOXYLIC ACID TESTER PRODRUG HEMMER FROM MEK |
| WO2015039606A1 (en) | 2013-09-18 | 2015-03-26 | The Hong Kong Polytechnic University | Novel phosphines, synthesis thereof and their use in catalysis |
| RU2646758C2 (ru) | 2013-12-05 | 2018-03-07 | Ф. Хоффманн-Ля Рош Аг | Гетероарил пиридоны и азапиридоны с электрофильной функциональностью |
| CN103819369B (zh) * | 2014-03-11 | 2016-06-01 | 杨雪飞 | 一种苯磺酰胺类化合物的合成方法 |
| KR20160127140A (ko) | 2014-03-18 | 2016-11-02 | 에프. 호프만-라 로슈 아게 | 옥세판-2-일-피라졸-4-일-헤테로사이클릴-카복사마이드 화합물 및 사용 방법 |
| US9394387B2 (en) | 2014-05-15 | 2016-07-19 | Chevron Phillips Chemical Company Lp | Synthesis of aryl coupled bis phenoxides and their use in olefin polymerization catalyst systems with activator-supports |
| WO2016094489A1 (en) | 2014-12-10 | 2016-06-16 | The Regents Of The University Of California | Phosphorus ligands and methods of use |
| CN106588983B (zh) * | 2015-10-14 | 2021-10-01 | 香港理工大学深圳研究院 | 咔唑基磷配体、及其制备方法和应用 |
| CN105273006B (zh) * | 2015-11-02 | 2017-09-19 | 盘锦格林凯默科技有限公司 | 2‑二环己基膦‑2,4,6‑三异丙基联苯的制备方法 |
| US20170173569A1 (en) | 2015-12-16 | 2017-06-22 | Bruce H. Lipshutz | Fe-ppm Pd, Cu and/or Ni Nanoparticle-Catalyzed Reactions in Water |
| WO2018081672A1 (en) | 2016-10-31 | 2018-05-03 | The Regents Of The University Of California | Biaryl ligands for transition metal-catalyzed reactions |
| CN109956970A (zh) * | 2017-12-26 | 2019-07-02 | 南开大学 | 联苯型三齿配体钌络合物及其制备方法和应用 |
| CN110240616B (zh) | 2018-03-07 | 2021-03-23 | 东莞市均成高新材料有限公司 | 三联芳单膦配体、它们的制备方法和在催化偶联反应中的用途 |
| JP7041092B2 (ja) | 2019-04-05 | 2022-03-23 | 日本化学工業株式会社 | ビアリールホスフィンの製造方法 |
| CN113019463B (zh) * | 2021-05-25 | 2021-09-07 | 江苏欣诺科催化剂有限公司 | 钯复合催化剂及其制备方法和应用 |
| EP4665495A1 (en) * | 2023-02-15 | 2025-12-24 | Indian Institute of Technology Bombay | Development of ligands for metals and metal-catalyzed reactions |
| WO2024191833A2 (en) * | 2023-03-10 | 2024-09-19 | Flexsys America L.P. | Quinolineimine antidegradant compounds and uses thereof |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030163003A1 (en) * | 1999-08-23 | 2003-08-28 | The Penn State Research Foundation | Chiral ligands, transition-metal complexes thereof and uses thereof in asymmetric reactions |
| US20060173186A1 (en) * | 2005-01-10 | 2006-08-03 | Massachusetts Institute Of Technology | Transition-metal-catalyzed carbon-nitrogen and carbon-carbon bond-forming reactions |
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| JPS51132190A (en) | 1975-03-04 | 1976-11-17 | Agency Of Ind Science & Technol | Complex catalist for asymmetric reaction |
| SE449456B (sv) * | 1983-11-15 | 1987-05-04 | Uponor Ab | Forfarande och anordning for framstellning av ror varvid formbacksdelarna er delade i formstreckans lengsriktning |
| US4885376A (en) | 1987-10-13 | 1989-12-05 | Iowa State University Research Foundation, Inc. | New types of organometallic reagents and catalysts for asymmetric synthesis |
| JP2733880B2 (ja) | 1991-03-12 | 1998-03-30 | 高砂香料工業株式会社 | 光学活性三級ホスフィン化合物およびこれを配位子とする遷移金属錯体 |
| JP2939510B2 (ja) | 1991-10-04 | 1999-08-25 | 一雄 阿知波 | 新規な非対称軸不斉アミノホスフィン誘導体 |
| US5739396A (en) | 1991-12-09 | 1998-04-14 | Stanford University | Asymmetric ligands useful for transition metal catalyzed bond forming reactions |
| EP0582692B1 (de) * | 1992-01-31 | 1998-04-22 | F. Hoffmann-La Roche Ag | Diphosphinliganden |
| US5530150A (en) | 1993-03-12 | 1996-06-25 | Takasago International Corporation | Phosphine compound, complex containing the phosphine compound as ligand, process for producing optically active aldehyde using the phosphine compound or the complex, and 4-[(R)-1'-formylethyl]azetidin-2-one derivatives |
| DE4338826A1 (de) | 1993-11-13 | 1995-05-18 | Hoechst Ag | Verfahren zur Herstellung von 1,1`-Binaphthylen |
| JPH07330786A (ja) | 1994-06-09 | 1995-12-19 | Sumitomo Chem Co Ltd | 光学活性3級ホスフィン化合物、これを配位子とする遷移金属錯体およびこれを用いる製造法 |
| DE4435189A1 (de) | 1994-09-30 | 1996-04-04 | Hoechst Ag | Neue sulfonierte Phosphine, Verfahren zu ihrer Herstellung und ihre Verwendung als Bestandteil von Katalysatorsystemen |
| US5621129A (en) | 1995-03-09 | 1997-04-15 | Sumitomo Chemical Co., Ltd. | Optically active tertiary phosphine compound, transition metal complex comprising the same as ligand and process for preparing optically active organic silicon compound using said transition metal complex |
| US5508458A (en) | 1995-05-26 | 1996-04-16 | Hoechst Celanese Corporation | Chiral catalysts and processes for preparing the same |
| US5567856A (en) | 1995-05-30 | 1996-10-22 | Hoechst Celanese Corporation | Synthesis of and hydroformylation with fluoro-substituted bidentate phosphine ligands |
| AU7446196A (en) | 1995-10-13 | 1997-04-30 | Penn State Research Foundation, The | Asymmetric synthesis catalyzed by transition metal complexes with new chiral ligands |
| JP3430775B2 (ja) | 1996-03-01 | 2003-07-28 | 住友化学工業株式会社 | 3級ホスフィン化合物、これを配位子とする遷移金属錯体およびその用途 |
| JP3431749B2 (ja) | 1996-03-07 | 2003-07-28 | 高砂香料工業株式会社 | 新規な1−置換−2−ジフェニルホスフィノナフタレンおよびこれを配位子とする遷移金属錯体 |
| US5929281A (en) | 1996-04-19 | 1999-07-27 | Tosoh Corporation | Process for producing heterocyclic aromatic amine or arylamine |
| US5817877A (en) | 1996-09-23 | 1998-10-06 | Yale University | Metal-catalyzed amination of organic sulfonates to organic amines |
| US5847166A (en) | 1996-10-10 | 1998-12-08 | Massachusetts Institute Of Technology | Synthesis of aryl ethers |
| EP0849274A1 (en) | 1996-12-20 | 1998-06-24 | Schering Aktiengesellschaft | Bissteroidal compounds and their use for the preparation of chiral complexes |
| US6395916B1 (en) * | 1998-07-10 | 2002-05-28 | Massachusetts Institute Of Technology | Ligands for metals and improved metal-catalyzed processes based thereon |
| US7223879B2 (en) | 1998-07-10 | 2007-05-29 | Massachusetts Institute Of Technology | Ligands for metals and improved metal-catalyzed processes based thereon |
| US6307087B1 (en) | 1998-07-10 | 2001-10-23 | Massachusetts Institute Of Technology | Ligands for metals and improved metal-catalyzed processes based thereon |
| US6100398A (en) | 1998-10-14 | 2000-08-08 | Yale University | Transition metal-catalyzed process for preparing N-aryl amine compounds |
| WO2001000581A1 (en) * | 1999-06-30 | 2001-01-04 | The Penn State Research Foundation | Ligands based on chiral 2-amino-2'-hydroxy-1,1'-binaphthyl and related frameworks for asymmetric catalysis |
| WO2003006420A1 (en) | 2001-07-12 | 2003-01-23 | Yale University | Catalytic method to convert aryl compounds to aryl amines |
| EP2583958B1 (en) * | 2002-12-09 | 2016-08-10 | Massachusetts Institute of Technology (MIT) | Ligands for metals and improved metal-catalyzed processes based thereon |
| US7833927B2 (en) * | 2005-08-31 | 2010-11-16 | Rohm And Haas Company | Single site palladium catalyst complexes |
| DE102005046344A1 (de) * | 2005-09-28 | 2007-03-29 | Saltigo Gmbh | Verfahren zur Kupplung von Benzylaminen mit Halogenaromaten |
-
2008
- 2008-12-12 EP EP08860439.2A patent/EP2231680B1/en active Active
- 2008-12-12 WO PCT/US2008/086651 patent/WO2009076622A2/en not_active Ceased
- 2008-12-12 JP JP2010538198A patent/JP5591714B2/ja active Active
- 2008-12-12 CN CN200880126921.5A patent/CN101952298B/zh active Active
- 2008-12-12 CA CA2708369A patent/CA2708369C/en active Active
- 2008-12-12 US US12/334,083 patent/US7858784B2/en active Active
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030163003A1 (en) * | 1999-08-23 | 2003-08-28 | The Penn State Research Foundation | Chiral ligands, transition-metal complexes thereof and uses thereof in asymmetric reactions |
| US20060173186A1 (en) * | 2005-01-10 | 2006-08-03 | Massachusetts Institute Of Technology | Transition-metal-catalyzed carbon-nitrogen and carbon-carbon bond-forming reactions |
Non-Patent Citations (3)
| Title |
|---|
| A Practical Transition Metal-Free Aryl-Aryl Coupling Method :Arynes as Key Intermediates;Frédéric R.Leroux et al.;《Adv. Synth. Catal.》;20071004;第349卷;第2705-2713页 * |
| Bradley O. Ashburn et al..Synthesis of Tetra-ortho-substituted, Phosphorus-Containing and Carbonyl-Containing Biaryls Utilizing a Diels-Alder Approach.《J. Am. Chem. Soc.》.2007,第129卷(第29期), * |
| Synthesis of Tetra-ortho-substituted, Phosphorus-Containing and Carbonyl-Containing Biaryls Utilizing a Diels-Alder Approach;Bradley O. Ashburn et al.;《J. Am. Chem. Soc.》;20070629;第129卷(第29期);第9109-9116页 * |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2011508726A (ja) | 2011-03-17 |
| CN101952298A (zh) | 2011-01-19 |
| US7858784B2 (en) | 2010-12-28 |
| CA2708369A1 (en) | 2009-06-18 |
| CA2708369C (en) | 2017-04-04 |
| US20090221820A1 (en) | 2009-09-03 |
| WO2009076622A3 (en) | 2010-08-12 |
| EP2231680A4 (en) | 2012-05-30 |
| JP5591714B2 (ja) | 2014-09-17 |
| EP2231680A2 (en) | 2010-09-29 |
| EP2231680B1 (en) | 2018-03-28 |
| WO2009076622A2 (en) | 2009-06-18 |
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