Search results for "cyclopentadiene"

showing 10 items of 49 documents

Preparation and structure of pyrrolo[2,1-b]- and isoindolo[1,2-b][3,1]epoxyquinazolines

2007

Abstract Various γ-oxocarboxylic acids [aroylpropionic acids, cis-2-(4-methylbenzoyl)cyclohexanecarboxylic acid, diendo-3-benzoylbicyclo[2.2.1] heptane-2-carboxylic acid, formylbenzoic acid, methanobenzenecyclooctencarboxylic acid and the cyclopentadiene adduct of 3-trans-(4-methylbenzoyl)acrylic acid] were reacted with diexo-3-aminomethyl-7-oxabicyclo[2.2.1]hept-5-en-2-ylamine 2 to result in condensed pyrroloepoxyquinazolines 3–10. The starting 2 retained the diexo configuration, but cis → trans isomerization took place when cis-2-(4-methylbenzoyl)cyclohexanecarboxylic acid was applied. The structures, including the ring annelations and the position of the aryl group on the new chiral cent…

CyclopentadieneStereochemistryArylOrganic ChemistryDiastereomerNuclear magnetic resonance spectroscopyCyclohexanecarboxylic acidMedicinal chemistryAnalytical ChemistryAdductInorganic Chemistrychemistry.chemical_compoundchemistryIsomerizationSpectroscopyAcrylic acidJournal of Molecular Structure
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Linked cyclopentadienyl-amido titanium catalysts supported on pyridylethylsilane-modified silica for heterogeneous ethylene homo- and copolymerization

2003

Abstract Linked cyclopentadienyl-amido titanium dimethyl and dichloro complexes, Ti(η 5 :η 1 -C 5 Me 4 SiMe 2 N t Bu)X 2 (X=Me, Cl), were reacted with trityl tetrakis(pentafluorophenyl)borate (TB), Ph 3 C + [B(C 6 F 5 ) 4 ] − , and methylaluminoxane (MAO), followed by treatment with toluene suspension of pyridylethylsilane-modified silica, to give two new supported-type titanium catalysts, PySTiTB and PySTiMAO. PySTiTB polymerized ethylene in the presence of triisobutylaluminum (TIBA) in hexane at 60 °C and 5 bar with slightly higher activity than the corresponding homogeneous system under the same conditions. PySTiMAO showed relatively high activity even without any use of alkylaluminum co…

EthyleneCyclopentadieneProcess Chemistry and TechnologyMethylaluminoxanechemistry.chemical_elementPolyethyleneCatalysisCatalysischemistry.chemical_compoundCyclopentadienyl complexchemistryPolymer chemistryCopolymerPhysical and Theoretical ChemistryTitaniumJournal of Molecular Catalysis A: Chemical
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Synthèse et caractérisation de phosphine, borane, amine sur plateforme ferrocène polyfonctionnelle

2016

Ferrocene platforms are useful in coordination chemistry and catalysis thanks to their robustness and versatile functionalization. Ferrocene backbone allows the implantation of several key functional groups in a restricted space, inducing close proximity and potential polyfunctional cooperation (see for instance ferrocenyl polyphosphine chemistry). Ansa ferrocene and ferrocene bearing conformational control inducing groups maximizing the proximity of key groups have been widely reported.The first part of this thesis focuses on the synthesis of new borylated cyclopentadienyl, and their use in formation of borylated metallocenes bearing conformational constraints. NMR analysis and DFT calcula…

Frustrated Lewis pairAmbiphilic ligandCouplage de spinPhosphorusPaire frustrée de Lewis[CHIM.COOR] Chemical Sciences/Coordination chemistryCyclopentadiénureCyclopentadienideBorePhosphore[CHIM.COOR]Chemical Sciences/Coordination chemistryFerroceneNon-bonded spin couplingLigand ambiphileAmineCyclopentadieneBoronMetallocene
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On the enhancement of stereoselection by cooperation between chiral auxiliaries. Asymmetric diels-alder reactions with fumaric acid bis ((S)-proline …

1989

Abstract Fumaric acid bis ((S)-proline benzyl ester) amide reacts with cyclopentadiene in thermal and Lewis acid catalyzed Diels-Alder reactions to give the cycloadducts with high yields and diastereomeric ratios up to 100:1.

Fumaric acidCyclopentadieneOrganic ChemistryDiastereomerBiochemistryCatalysischemistry.chemical_compoundchemistryAmideDrug DiscoveryDiels alderOrganic chemistryLewis acids and basesProline benzyl esterTetrahedron Letters
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Cationic Iron Aminocarbene Complexes as Dienophiles in Diels‐Alder Reaction with Cyclopentadiene

1996

The cationic iron (alkynyl)aminocarbene complexes [Cp(CO)2Fe(C(NHR)CCSiMe3][PF6], (R C6H5, p-CH3C6H4) 1 derived from aromatic amines smoothly react with cyclopentadiene in dichloromethane to yield the cycloadducts 2. No reaction was observed for complexes derived from sterically demanding aliphatic amines, like L-alanine tert-butyl ester. For comparison, the alkynyl-substituted acyl iron compounds Cp(CO)2Fe(CO)CC (R SiMe3, C6H5) 3 were investigated, requiring TiCl4 catalysis to undergo the cycloaddition reaction. The structures of the cycloadducts 4 were determined by X-ray crystallography.

Inorganic ChemistrySteric effectschemistry.chemical_compoundCyclopentadieneChemistryYield (chemistry)Cationic polymerizationOrganic chemistryMedicinal chemistryCycloadditionDiels–Alder reactionCatalysisDichloromethaneChemische Berichte
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Isomerisierung der Dihydropentalene und Umsetzung mit Tetracyanethylen

1987

Zwischen den sechs isomeren Dihydropentalenen 1–6 existieren eine Reihe von H-Verschiebungen (Schema 1), die in Gasphasenpyrolysen untersucht werden. Der thermodynamisch kontrollierte irreversible Ausgang aus den Gleichgewichten von 1–6 fuhrt uber 1-Vinylfulven (14) zu Styrol (15). Praparativ nutzlich ist besonders die katalytische Isomerisierung zwischen 1,5-DHP (4) und 1,2-DHP (1) bei Raumtemperatur. Die Umsetzung der Dihydropentalene mit Tetracyanethylen liefert bei 1 das [2+2]-Addukt 24, bei 3 und 5 die [4+2]-Addukte 25 bzw. 26 und bei 4 das doppelte [4+2]-Addukt 22.2 und 6 lassen sich unter Blitzpyrolyse-Bedingungen mit TCNE nicht abfangen. Isomerization of Dihydropentalenes and Reacti…

Inorganic Chemistrychemistry.chemical_compoundCyclopentadieneBicyclic moleculeNitrileChemistryStereochemistryNuclear magnetic resonance spectroscopyTetracyanoethyleneMedicinal chemistryIsomerizationStyreneAdductChemische Berichte
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Influence of structural factors and enzyme type on the reactivity and enantioselectivity of the enzymatic esterification of bicyclic meso dialcohols

1992

The meso dialcohols 1–7, obtained from the Diels-Alder adducts furan/maleic anhydride, furan/dimethyl acetylenedi-carboxylate, and cyclopentadiene/maleic anhydride, were subjected to enzymatic esterification in organic solvents. A mixture of the corresponding chiral monoacetates and the meso diacetates was obtained. It has been found that reaction rate and enantioselectivity markedly depend on substrate structure, temperature, enzyme type, and nature of the solvent. The presence of an oxygen bridge and an exo configuration are the two structural features which lead to the highest enantioselectivity values.

Inorganic Chemistrychemistry.chemical_compoundCyclopentadienechemistryBicyclic moleculeMeso compoundFuranMaleic anhydrideSubstrate (chemistry)Organic chemistryReactivity (chemistry)Solvent effectsChemische Berichte
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New practical tungsten(VI) based catalyst systems for ring opening metathesis polymerisation

2002

Abstract Tungsten(VI) complexes of the type trans -[WCl 2 (diol)(OAr) 2 ] were studied as catalyst precursors for ROMP of norbornene and dicyclopentadiene. These compounds form active catalysts when treated by simple Grignard reagents, such as methyl magnesium iodide or neophyl magnesium chloride. Moreover, polymerisations can be run under ambient atmosphere without complicated inert atmosphere techniques.

MagnesiumDiolchemistry.chemical_elementROMPMagnesium iodideCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryDicyclopentadieneMaterials ChemistryOrganic chemistryRing-opening metathesis polymerisationPhysical and Theoretical ChemistryNorborneneInorganic Chemistry Communications
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From Pentalene to Dicyclopenta[b,g]naphthalene, or the Change towards Delocalized Structures

2005

Lining triples-corrected coupled-cluster methods as well as other high-level theoretical approximations, the optimized parameters and isomerization barriers of the family of compounds cyclopentadiene-(benzene) x -cyclopentadiene (x 0, 1, 2) are computed. In contrast to previous studies, s-indacene presents a localized C 2 h geometry. Also, the localized structure of pentalene is found to be the most stable, but when two benzene rings are intercalated between the five-member rings of pentalene, the resulting molecule preferably adopts a delocalized D 2 h conformation.

PentaleneCyclopentadieneChemistryAromaticityElectronic structureAtomic and Molecular Physics and OpticsCrystallographyDelocalized electronchemistry.chemical_compoundComputational chemistryAb initio quantum chemistry methodsMoleculePhysical and Theoretical ChemistryIsomerizationpentalene; dicyclopenta[b; g]naphthaleneChemPhysChem
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Understanding the mechanism of non-polar diels-alder reactions. A comparative elf analysis of concerted and stepwise diradical mechanisms

2010

The electron-reorganization along the concerted and stepwise pathways associated with the non-polar Diels-Alder reaction between cyclopentadiene (Cp, 1) and ethylene (2) has been studied using the topological analysis of the electron localization function (ELF) at the B3LYP/6-31G(d) level of theory. ELF results for the concerted mechanism stresses that the electron-reorganization demanded on the diene and ethylene reagents to reach two pseudo-diradical structures is responsible for the high activation energy. A comparative ELF analysis of some relevant points of the non-polar Diels-Alder reaction between Cp and styrene (10) suggests that these concerted mechanisms do not have a pericyclic e…

Pericyclic reactionEthyleneCyclopentadieneDieneDiradicalConcerted reactionStereochemistryOrganic Chemistryrespiratory systemBiochemistryElectron localization functionStyrenechemistry.chemical_compoundchemistryPhysical and Theoretical Chemistry
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