DE60238367D1 - Asymmetrischer Kupferkomplex und dessen Verwendung in Cyclopropanierungsreaktion - Google Patents

Asymmetrischer Kupferkomplex und dessen Verwendung in Cyclopropanierungsreaktion

Info

Publication number
DE60238367D1
DE60238367D1 DE60238367T DE60238367T DE60238367D1 DE 60238367 D1 DE60238367 D1 DE 60238367D1 DE 60238367 T DE60238367 T DE 60238367T DE 60238367 T DE60238367 T DE 60238367T DE 60238367 D1 DE60238367 D1 DE 60238367D1
Authority
DE
Germany
Prior art keywords
group
represent
hydrogen atom
copper complex
alkyl group
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 - Lifetime
Application number
DE60238367T
Other languages
German (de)
English (en)
Inventor
Michio Yamamoto
Gohfu Suzukamo
Makoto Itagaki
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo Chemical Co Ltd
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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Application granted granted Critical
Publication of DE60238367D1 publication Critical patent/DE60238367D1/de
Anticipated expiration legal-status Critical
Expired - Lifetime 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
    • C07F1/00Compounds containing elements of Groups 1 or 11 of the Periodic Table
    • C07F1/08Copper compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F1/00Compounds containing elements of Groups 1 or 11 of the Periodic Table
    • C07F1/005Compounds containing elements of Groups 1 or 11 of the Periodic Table without C-Metal linkages
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • B01J31/18Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms
    • B01J31/1805Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes containing nitrogen, phosphorus, arsenic or antimony as complexing atoms, e.g. in pyridine ligands, or in resonance therewith, e.g. in isocyanide ligands C=N-R or as complexed central atoms the ligands containing nitrogen
    • B01J31/181Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine
    • B01J31/1815Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine with more than one complexing nitrogen atom, e.g. bipyridyl, 2-aminopyridine
    • B01J31/182Cyclic ligands, including e.g. non-condensed polycyclic ligands, comprising at least one complexing nitrogen atom as ring member, e.g. pyridine with more than one complexing nitrogen atom, e.g. bipyridyl, 2-aminopyridine comprising aliphatic or saturated rings
    • 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
    • C07C67/347Preparation 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 by addition to unsaturated carbon-to-carbon bonds
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/30Addition reactions at carbon centres, i.e. to either C-C or C-X multiple bonds
    • B01J2231/32Addition reactions to C=C or C-C triple bonds
    • B01J2231/324Cyclisations via conversion of C-C multiple to single or less multiple bonds, e.g. cycloadditions
    • B01J2231/325Cyclopropanations
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/10Complexes comprising metals of Group I (IA or IB) as the central metal
    • B01J2531/16Copper
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/06Halogens; Compounds thereof
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/0231Halogen-containing compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07Optical isomers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
DE60238367T 2001-04-27 2002-04-23 Asymmetrischer Kupferkomplex und dessen Verwendung in Cyclopropanierungsreaktion Expired - Lifetime DE60238367D1 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2001132016 2001-04-27

Publications (1)

Publication Number Publication Date
DE60238367D1 true DE60238367D1 (de) 2011-01-05

Family

ID=18980097

Family Applications (1)

Application Number Title Priority Date Filing Date
DE60238367T Expired - Lifetime DE60238367D1 (de) 2001-04-27 2002-04-23 Asymmetrischer Kupferkomplex und dessen Verwendung in Cyclopropanierungsreaktion

Country Status (9)

Country Link
US (1) US6858559B2 (enExample)
EP (1) EP1253135B1 (enExample)
KR (1) KR20020083457A (enExample)
CN (1) CN1259322C (enExample)
AT (1) ATE489356T1 (enExample)
DE (1) DE60238367D1 (enExample)
ES (1) ES2354685T3 (enExample)
HU (1) HU229387B1 (enExample)
ZA (1) ZA200203301B (enExample)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7288674B2 (en) 2003-02-07 2007-10-30 Sumitomo Chemical Company, Limited Optically active bisoxazoline compounds, process for production of the same and use thereof
PL1607136T3 (pl) * 2003-03-31 2012-09-28 Sumitomo Chemical Co Kompozycja optycznie czynnego katalizatora miedziowego
ZA200602753B (en) * 2003-09-19 2007-06-27 Sumitomo Chemical Co Process for producing optically active cycloprop compound and asymmetric copper complex for use in same
ITMI20041211A1 (it) * 2004-06-16 2004-09-16 Endura Spa Catalizzatori a base di complessi metallici per la sintesi di acido crisantemico otticamente attivo
ZA200700028B (en) * 2004-07-01 2008-05-28 Sumitomo Chemical Co Method for producing optically active cyclopropaneca boxylate compound
JP5002916B2 (ja) * 2004-07-01 2012-08-15 住友化学株式会社 不斉銅錯体およびそれを用いた光学活性なシクロプロパンカルボン酸エステル化合物の製造方法
CN100389117C (zh) * 2004-08-20 2008-05-21 中国科学院上海有机化学研究所 一种具有手性中心的噁唑啉环金属催化剂、合成及用途
CN100348597C (zh) * 2005-12-29 2007-11-14 上海交通大学 5,5’位连接的1, 1’-联苯类轴手性配体的合成方法
ES2721446T3 (es) * 2008-09-10 2019-07-31 Sumitomo Chemical Co Método para producir un compuesto de éster del ácido ciclopropano carboxílico ópticamente activo, un complejo de cobre asimétrico y un compuesto de salicilidenoaminoalcohol ópticamente activo
CN104926747B (zh) * 2015-06-01 2018-09-21 中国科学院上海有机化学研究所 具有光学活性的环己基噁唑啉配体的合成方法及其用途
CN106045985B (zh) * 2016-06-14 2018-11-09 华中师范大学 一种双噁唑啉类化合物及制备方法和用途
CN109692708A (zh) * 2017-10-24 2019-04-30 沈阳中化农药化工研发有限公司 一种不对称环丙化催化剂及其应用
CN111732508B (zh) * 2019-03-25 2022-11-01 华东师范大学 一种螺环化合物的合成方法
CN114369248B (zh) * 2020-10-15 2022-09-02 中国科学院大连化学物理研究所 一种手性含硅聚酯及其合成方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4033976A (en) * 1975-10-28 1977-07-05 Imc Chemical Group, Inc. Copper-oxazoline complex
HU210648B (en) 1983-09-15 1995-06-28 Jozsef Muskovits Process for preparing cycloproane-carboxylic acid esters
US5298623A (en) 1991-11-08 1994-03-29 Massachusetts Institute Of Technology Cu complexes of bis-oxazolines and their use
US6011169A (en) 1997-07-14 2000-01-04 Sumitomo Chemical Company, Limited Process for producing optically active cyclopropanecaboxylic acid esters
CA2244417C (en) * 1997-08-05 2006-07-18 Sumitomo Chemical Co., Ltd. Optically active bisoxazoline compounds, production and use thereof
GB9725455D0 (en) * 1997-12-02 1998-01-28 Univ Warwick Supported polymerisation catalyst
CN1491235A (zh) * 2001-02-17 2004-04-21 赛拉尼斯温特斯股份有限公司 作为催化剂组分的过渡金属化合物及其在生产聚烯烃中的用途

Also Published As

Publication number Publication date
ATE489356T1 (de) 2010-12-15
CN1384105A (zh) 2002-12-11
EP1253135A1 (en) 2002-10-30
KR20020083457A (ko) 2002-11-02
CN1259322C (zh) 2006-06-14
HU0201357D0 (enExample) 2002-06-29
HU229387B1 (en) 2013-11-28
US6858559B2 (en) 2005-02-22
HUP0201357A3 (en) 2004-06-28
EP1253135B1 (en) 2010-11-24
ES2354685T3 (es) 2011-03-17
US20020177718A1 (en) 2002-11-28
ZA200203301B (en) 2002-12-04
HUP0201357A2 (hu) 2003-01-28

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