HU0201357D0 - - Google Patents

Info

Publication number
HU0201357D0
HU0201357D0 HU0201357A HUP0201357A HU0201357D0 HU 0201357 D0 HU0201357 D0 HU 0201357D0 HU 0201357 A HU0201357 A HU 0201357A HU P0201357 A HUP0201357 A HU P0201357A HU 0201357 D0 HU0201357 D0 HU 0201357D0
Authority
HU
Hungary
Prior art keywords
group
represent
hydrogen atom
alkyl group
phenyl
Prior art date
Application number
HU0201357A
Other languages
English (en)
Hungarian (hu)
Original Assignee
Sumitomo Chemical Co
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 filed Critical Sumitomo Chemical Co
Publication of HU0201357D0 publication Critical patent/HU0201357D0/hu
Publication of HUP0201357A2 publication Critical patent/HUP0201357A2/hu
Publication of HUP0201357A3 publication Critical patent/HUP0201357A3/hu
Publication of HU229387B1 publication Critical patent/HU229387B1/hu

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
    • C07F1/005Compounds containing elements of Groups 1 or 11 of the Periodic Table without C-Metal linkages
    • 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
    • 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)
HU0201357A 2001-04-27 2002-04-24 Process for preparing cyclopropan carboxylate derivatives using asymmetric copper complex HU229387B1 (en)

Applications Claiming Priority (1)

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

Publications (4)

Publication Number Publication Date
HU0201357D0 true HU0201357D0 (enExample) 2002-06-29
HUP0201357A2 HUP0201357A2 (hu) 2003-01-28
HUP0201357A3 HUP0201357A3 (en) 2004-06-28
HU229387B1 HU229387B1 (en) 2013-11-28

Family

ID=18980097

Family Applications (1)

Application Number Title Priority Date Filing Date
HU0201357A HU229387B1 (en) 2001-04-27 2002-04-24 Process for preparing cyclopropan carboxylate derivatives using asymmetric copper complex

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
KR101137746B1 (ko) 2003-02-07 2012-04-24 스미또모 가가꾸 가부시끼가이샤 광학 활성 비스옥사졸린 화합물, 그 제조 방법 및 그 용도
PL1607136T3 (pl) * 2003-03-31 2012-09-28 Sumitomo Chemical Co Kompozycja optycznie czynnego katalizatora miedziowego
KR101132998B1 (ko) * 2003-09-19 2012-04-10 스미또모 가가꾸 가부시끼가이샤 광학 활성 시클로프로판 화합물의 제조 방법 및 이에사용된 비대칭 구리 착물
ITMI20041211A1 (it) * 2004-06-16 2004-09-16 Endura Spa Catalizzatori a base di complessi metallici per la sintesi di acido crisantemico otticamente attivo
US7705165B2 (en) * 2004-07-01 2010-04-27 Sumitomo Chemical Company, Limited Method for producing optically active cyclopropanecarboxylate 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
SG193207A1 (en) * 2008-09-10 2013-09-30 Sumitomo Chemical Co Method for producing optically active cyclopropane carboxylic acid ester compound, asymmetric copper complex, and optically active salicylideneaminoalcohol compound
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
EP1368385A1 (de) * 2001-02-17 2003-12-10 Celanese Ventures GmbH Übergangsmetallverbindung als katalysatorbestandteil, und verwendung zur herstellung von polyolefinen

Also Published As

Publication number Publication date
HU229387B1 (en) 2013-11-28
HUP0201357A3 (en) 2004-06-28
ATE489356T1 (de) 2010-12-15
HUP0201357A2 (hu) 2003-01-28
CN1384105A (zh) 2002-12-11
ZA200203301B (en) 2002-12-04
US20020177718A1 (en) 2002-11-28
KR20020083457A (ko) 2002-11-02
ES2354685T3 (es) 2011-03-17
CN1259322C (zh) 2006-06-14
DE60238367D1 (de) 2011-01-05
US6858559B2 (en) 2005-02-22
EP1253135A1 (en) 2002-10-30
EP1253135B1 (en) 2010-11-24

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Legal Events

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MM4A Lapse of definitive patent protection due to non-payment of fees