PL442226A1 - Nowe kompleksy rutenu, sposób ich otrzymywania, związki pośrednie stosowane w tym sposobie, sposób ich wytwarzania oraz zastosowanie nowych kompleksów rutenu w reakcjach metatezy olefin - Google Patents

Nowe kompleksy rutenu, sposób ich otrzymywania, związki pośrednie stosowane w tym sposobie, sposób ich wytwarzania oraz zastosowanie nowych kompleksów rutenu w reakcjach metatezy olefin

Info

Publication number
PL442226A1
PL442226A1 PL442226A PL44222622A PL442226A1 PL 442226 A1 PL442226 A1 PL 442226A1 PL 442226 A PL442226 A PL 442226A PL 44222622 A PL44222622 A PL 44222622A PL 442226 A1 PL442226 A1 PL 442226A1
Authority
PL
Poland
Prior art keywords
ruthenium complexes
new ruthenium
obtaining
preparation
olefin metathesis
Prior art date
Application number
PL442226A
Other languages
English (en)
Inventor
Anna KAJETANOWICZ
Adrian SYTNICZUK
Filip STRUZIK
Original Assignee
Uniwersytet Warszawski
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 Uniwersytet Warszawski filed Critical Uniwersytet Warszawski
Priority to PL442226A priority Critical patent/PL442226A1/pl
Priority to PCT/IB2023/058921 priority patent/WO2024052871A1/en
Publication of PL442226A1 publication Critical patent/PL442226A1/pl

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • B01J31/22Organic complexes
    • 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
    • B01J31/22Organic complexes
    • B01J31/2204Organic complexes the ligands containing oxygen or sulfur as complexing atoms
    • B01J31/2208Oxygen, e.g. acetylacetonates
    • 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
    • B01J31/22Organic complexes
    • B01J31/2265Carbenes or carbynes, i.e.(image)
    • B01J31/2269Heterocyclic carbenes
    • B01J31/2273Heterocyclic carbenes with only nitrogen as heteroatomic ring members, e.g. 1,3-diarylimidazoline-2-ylidenes
    • 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
    • B01J31/22Organic complexes
    • B01J31/2265Carbenes or carbynes, i.e.(image)
    • B01J31/2278Complexes comprising two carbene ligands differing from each other, e.g. Grubbs second generation catalysts
    • 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
    • B01J31/22Organic complexes
    • B01J31/2282Unsaturated compounds used as ligands
    • B01J31/2295Cyclic compounds, e.g. cyclopentadienyls
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C37/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C6/00Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
    • C07C6/02Metathesis reactions at an unsaturated carbon-to-carbon bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C6/00Preparation of hydrocarbons from hydrocarbons containing a different number of carbon atoms by redistribution reactions
    • C07C6/02Metathesis reactions at an unsaturated carbon-to-carbon bond
    • C07C6/04Metathesis reactions at an unsaturated carbon-to-carbon bond at a carbon-to-carbon double bond
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/04Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D407/00Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/02Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
    • C07D407/04Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F15/00Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table
    • C07F15/0006Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic Table compounds of the platinum group
    • C07F15/0046Ruthenium compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F17/00Metallocenes
    • C07F17/02Metallocenes of metals of Groups 8, 9 or 10 of the Periodic Table
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F19/00Metal compounds according to more than one of main groups C07F1/00 - C07F17/00
    • 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
    • B01J2231/50Redistribution or isomerisation reactions of C-C, C=C or C-C triple bonds
    • B01J2231/54Metathesis reactions, e.g. olefin metathesis
    • B01J2231/543Metathesis reactions, e.g. olefin metathesis alkene metathesis
    • 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
    • B01J2531/02Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0202Polynuclearity
    • B01J2531/0205Bi- or polynuclear complexes, i.e. comprising two or more metal coordination centres, without metal-metal bonds, e.g. Cp(Lx)Zr-imidazole-Zr(Lx)Cp
    • 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
    • B01J2531/02Compositional aspects of complexes used, e.g. polynuclearity
    • B01J2531/0286Complexes comprising ligands or other components characterized by their function
    • B01J2531/0288Sterically demanding or shielding ligands
    • 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
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82Metals of the platinum group
    • B01J2531/821Ruthenium
    • 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
    • B01J2531/80Complexes comprising metals of Group VIII as the central metal
    • B01J2531/84Metals of the iron group
    • B01J2531/842Iron
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2540/00Compositional aspects of coordination complexes or ligands in catalyst systems
    • B01J2540/10Non-coordinating groups comprising only oxygen beside carbon or hydrogen
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2540/00Compositional aspects of coordination complexes or ligands in catalyst systems
    • B01J2540/30Non-coordinating groups comprising sulfur
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2531/00Catalysts comprising hydrides, coordination complexes or organic compounds
    • C07C2531/16Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
    • C07C2531/22Organic complexes

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)

Abstract

Przedmiotem zgłoszenia jest nowy kompleks rutenu o wzorze ogólnym Ru-1, w którym wszystkie zmienne podstawniki mają zdefiniowane w opisie znaczenia. Przedmiotem zgłoszenia jest także sposób otrzymywania kompleksu rutenu, związek pośredni będący prekursorem ligandu stosowany w otrzymywaniu kompleksu rutenu CAAC-1 oraz zastosowanie tego kompleksu rutenu jako (pre)katalizatora w reakcjach metatezy olefin.
PL442226A 2022-09-08 2022-09-08 Nowe kompleksy rutenu, sposób ich otrzymywania, związki pośrednie stosowane w tym sposobie, sposób ich wytwarzania oraz zastosowanie nowych kompleksów rutenu w reakcjach metatezy olefin PL442226A1 (pl)

Priority Applications (2)

Application Number Priority Date Filing Date Title
PL442226A PL442226A1 (pl) 2022-09-08 2022-09-08 Nowe kompleksy rutenu, sposób ich otrzymywania, związki pośrednie stosowane w tym sposobie, sposób ich wytwarzania oraz zastosowanie nowych kompleksów rutenu w reakcjach metatezy olefin
PCT/IB2023/058921 WO2024052871A1 (en) 2022-09-08 2023-09-08 Novel ruthenium complexes, method of their synthesis, intermediate compounds used in this method, method of their synthesis and use of novel ruthenium complexes in olefin metathesis reactions

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PL442226A PL442226A1 (pl) 2022-09-08 2022-09-08 Nowe kompleksy rutenu, sposób ich otrzymywania, związki pośrednie stosowane w tym sposobie, sposób ich wytwarzania oraz zastosowanie nowych kompleksów rutenu w reakcjach metatezy olefin

Publications (1)

Publication Number Publication Date
PL442226A1 true PL442226A1 (pl) 2024-03-11

Family

ID=88600293

Family Applications (1)

Application Number Title Priority Date Filing Date
PL442226A PL442226A1 (pl) 2022-09-08 2022-09-08 Nowe kompleksy rutenu, sposób ich otrzymywania, związki pośrednie stosowane w tym sposobie, sposób ich wytwarzania oraz zastosowanie nowych kompleksów rutenu w reakcjach metatezy olefin

Country Status (2)

Country Link
PL (1) PL442226A1 (pl)
WO (1) WO2024052871A1 (pl)

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2909381A1 (fr) * 2006-11-30 2008-06-06 Enscr Complexes de rethenium et utilisation de tels complexes pour la metathese d'olefines
CN101205242A (zh) * 2007-09-30 2008-06-25 埃沃尼克德古萨有限责任公司 含有n-杂环卡宾配体的钌的亚烷基络合物及其在烯烃复分解反应中作为高活性高选择性催化剂的用途
US20110306815A1 (en) * 2009-11-09 2011-12-15 Hagadorn John R Metathesis Catalyst and Process for Use Thereof
WO2017055945A1 (en) * 2015-09-30 2017-04-06 Apeiron Synthesis S.A. Process for producing ruthenium complexes and intermediates thereof and their use in olefin metathesis
PL419637A1 (pl) * 2016-11-30 2018-06-04 Uniwersytet Warszawski Nowy kompleks rutenu, sposób jego otrzymywania oraz zastosowanie w reakcji metatezy olefin
KR20210056130A (ko) * 2019-11-08 2021-05-18 광주과학기술원 루테늄 착물 형성을 위한 비고리형 카벤 리간드, 루테늄 착물 촉매 및 이의 용도
PL432325A1 (pl) * 2019-12-23 2021-06-28 Apeiron Synthesis Spółka Akcyjna Kompleks rutenu i sposób prowadzenia reakcji metatezy olefin z utworzeniem wiązania wewnętrznego z zastosowaniem kompleksu rutenu jako katalizatora
CN113735914A (zh) * 2021-08-24 2021-12-03 南方科技大学 二茂铁衍生物类金属有机配合物及其制备方法与应用

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2909381A1 (fr) * 2006-11-30 2008-06-06 Enscr Complexes de rethenium et utilisation de tels complexes pour la metathese d'olefines
CN101205242A (zh) * 2007-09-30 2008-06-25 埃沃尼克德古萨有限责任公司 含有n-杂环卡宾配体的钌的亚烷基络合物及其在烯烃复分解反应中作为高活性高选择性催化剂的用途
US20110306815A1 (en) * 2009-11-09 2011-12-15 Hagadorn John R Metathesis Catalyst and Process for Use Thereof
WO2017055945A1 (en) * 2015-09-30 2017-04-06 Apeiron Synthesis S.A. Process for producing ruthenium complexes and intermediates thereof and their use in olefin metathesis
EP3356379A1 (en) * 2015-09-30 2018-08-08 Apeiron Synthesis S.A. Process for producing ruthenium complexes and intermediates thereof and their use in olefin metathesis
PL419637A1 (pl) * 2016-11-30 2018-06-04 Uniwersytet Warszawski Nowy kompleks rutenu, sposób jego otrzymywania oraz zastosowanie w reakcji metatezy olefin
KR20210056130A (ko) * 2019-11-08 2021-05-18 광주과학기술원 루테늄 착물 형성을 위한 비고리형 카벤 리간드, 루테늄 착물 촉매 및 이의 용도
PL432325A1 (pl) * 2019-12-23 2021-06-28 Apeiron Synthesis Spółka Akcyjna Kompleks rutenu i sposób prowadzenia reakcji metatezy olefin z utworzeniem wiązania wewnętrznego z zastosowaniem kompleksu rutenu jako katalizatora
CN113735914A (zh) * 2021-08-24 2021-12-03 南方科技大学 二茂铁衍生物类金属有机配合物及其制备方法与应用

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
GAWIN R. I INN.: "Angew. Chem. Int. Ed. 2017, 56, 981-986", BIS(CYCLIC ALKYL AMINO CARBENE) RUTHENIUM COMPLEXES: A VERSATILE, HIGHLY EFFICIENT TOOL FOR OLEFIN METATHESIS *

Also Published As

Publication number Publication date
WO2024052871A1 (en) 2024-03-14

Similar Documents

Publication Publication Date Title
PL414234A1 (pl) Sposób wytwarzania kompleksów rutenu i związków pośrednich oraz ich zastosowanie w metatezie olefin
Wang et al. An Agostic Iridium Pincer Complex as a Highly Efficient and Selective Catalyst for Monoisomerization of 1‐Alkenes to trans‐2‐Alkenes
Zinser et al. A simple synthetic entryway into palladium cross-coupling catalysis
Camasso et al. Design, synthesis, and carbon-heteroatom coupling reactions of organometallic nickel (IV) complexes
Higuchi et al. Preparation and reactivity of iron complexes bearing anionic carbazole-based PNP-type pincer ligands toward catalytic nitrogen fixation
Wu et al. Stable gold (III) catalysts by oxidative addition of a carbon–carbon bond
Dias et al. Carbonyl and olefin adducts of coinage metals supported by poly (pyrazolyl) borate and poly (pyrazolyl) alkane ligands and silver mediated atom transfer reactions
Kim et al. Bis (imidazoline-2-thione)–copper (i) catalyzed regioselective boron addition to internal alkynes
Lin et al. Silver (I) N-heterocyclic carbenes
Banerjee et al. Gold-catalyzed 1, 2-oxyalkynylation of N-allenamides with ethylnylbenziodoxolones
Prieto et al. Gold-catalyzed olefin cyclopropanation
Chua et al. Selective Kumada biaryl cross-coupling reaction enabled by an iron (iii) alkoxide–N-heterocyclic carbene catalyst system
RU2015143202A (ru) Бис(2-инденил)металлоценовый комплекс
RU2014119148A (ru) Оксоалкилиденовые комплексы вольфрама для z-селективного метатезиса олефинов
PL442226A1 (pl) Nowe kompleksy rutenu, sposób ich otrzymywania, związki pośrednie stosowane w tym sposobie, sposób ich wytwarzania oraz zastosowanie nowych kompleksów rutenu w reakcjach metatezy olefin
Schachner et al. Dioxidomolybdenum (VI) and–tungsten (VI) complexes with tetradentate amino bisphenolates as catalysts for epoxidation
Hashmi Gold-catalyzed organic reactions
SA519401837B1 (ar) طريقة لتحضير محفز متجانس لإنتاج 1-هكسين انتقائي
Prakash et al. Efficient 1, 4-addition of α-substituted fluoro (phenylsulfonyl) methane derivatives to α, β-unsaturated compounds
Chen et al. Dealkenylative Ni-catalyzed cross-coupling enabled by tetrazine and photoexcitation
DE60323373D1 (de) Phosphor enthaltende ligande für metathese katalysatoren
Oakes et al. The surprisingly beneficial effect of soft donors on the performance of early transition metal olefin polymerisation catalysts
PL441535A1 (pl) Nowe kompleksy rutenu, sposób ich otrzymywania, związki pośrednie stosowane w tym sposobie, sposób ich wytwarzania oraz zastosowanie nowych kompleksów rutenu w reakcjach metatezy olefin
Willcox et al. Enantioselective 1, 4-additions of ClMeAl (CH [double bond, length as m-dash] CHR)(R= alkyl, alkenyl, Ph) to cyclohexenones
Ruiz et al. Selective formation of formamidines, carbodiimides and formimidates from isocyanide complexes of Mn (I) mediated by Ag 2 O