Search results for "REGIOSELECTIVITY"

showing 10 items of 298 documents

An Efficient Method for Controlled Propylene Oxide Polymerization: The Significance of Bimetallic Activation in Aluminum Lewis Acids

2009

chemistry.chemical_compoundPolymerizationchemistryAluminiumOrganic chemistrychemistry.chemical_elementRegioselectivityGeneral ChemistryLewis acids and basesPropylene oxideRing-opening polymerizationBimetallic stripCatalysisAngewandte Chemie International Edition
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Chemoselective reactions of N1-methyl-2-hydroxy-3-methylamino-3-phenylpropanamide with electrophiles. Synthesis of chiral hexahydro-4-pyrimidinones a…

2002

Abstract The reactivity of (2S,3S)-N1-methyl-2-hydroxy-3-methylamino-3-phenylpropanamide 1 , containing three nucleophilic centres has been studied against dihaloalkanes and aldehydes. Hexahydro-4-pyrimidinones or oxazolidines were obtained chemoselectively. Experimental results were explained by ‘ab initio’ calculations.

chemistry.chemical_compoundPyrimidinonesNucleophileChemistryOrganic ChemistryDrug DiscoveryElectrophileAb initioOrganic chemistryRegioselectivityReactivity (chemistry)BiochemistryDichloromethaneTetrahedron
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Density Functional Theory Study of the Cycloaddition Reaction of Furan Derivatives with Masked o-Benzoquinones. Does the Furan Act as a Dienophile in…

2002

The molecular mechanism for the cycloaddition reaction between 2-methylfuran and a masked o-benzoquinone has been characterized using quantum mechanical calculations at the B3LYP/6-31G theory level. An analysis of the results on the reaction pathway shows that the reaction takes place along a polar stepwise mechanism. The first and rate-determining step corresponds to the nucleophilic attack of the furan ring on the doubly conjugated position of the 2,4-dienone system present at the masked o-benzoquinone to give a zwitterionic intermediate. Closure of this intermediate affords the formally [2 + 4] cycloadduct. For the second step two reactive channels have been characterized corresponding t…

chemistry.chemical_compoundReaction mechanismchemistryNucleophileComputational chemistryStereochemistryFuranOrganic ChemistryElectrophileRegioselectivityReactivity (chemistry)Reaction intermediateCycloadditionThe Journal of Organic Chemistry
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Palladium-Catalyzed Suzuki Carbonylative Reaction of α-Halomethyl Oxime Ethers: A Regioselective Route to Unsymmetrical 1,3-Oxyiminoketones

2014

chemistry.chemical_compoundReaction mechanismchemistryRegioselectivitychemistry.chemical_elementOrganic chemistryGeneral ChemistryOximeCarbonylationPalladiumCatalysisAdvanced Synthesis & Catalysis
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ChemInform Abstract: 1,4-Regioselective Iodofunctionalizations of 1,3-Butadiene.

1989

1,3-Butadiene (I) is treated with a iodonium tetrafluoroborate in the presence of HBF4 and aqueous acetonitrile (II) or benzene (IV), yielding the 1,4-adducts (III) or (V).

chemistry.chemical_compoundTetrafluoroborateAqueous solutionchemistryRegioselectivity13-ButadieneGeneral MedicineAcetonitrileBenzeneMedicinal chemistryChemInform
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ChemInform Abstract: Acid-Mediated Reaction of Bis(pyridine)iodonium(I) Tetrafluoroborate with Aromatic Compounds. A Selective and General Iodination…

2010

Reaction of aromatic compounds with bis(pyridine)iodonium(I) tetrafluoroborate (IPy2BF4) in the presence of HBF4 or CF3SO3H in CH2Cl2 at room temperature furnishes monoiodo derivatives with excellent regioselectivity and yields. Use of either acid gives comparable results with activated aromatics, whereas CF3SO3H is much more effective in the iodination of deactivated aromatics. © 1993 American Chemical Society.

chemistry.chemical_compoundTetrafluoroboratechemistryPyridineHalogenationRegioselectivityGeneral MedicineMedicinal chemistryChemical societyBis(pyridine)iodonium(I) tetrafluoroborateChemInform
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Inside Cover: Synthesis and Application of β-Substituted Pauson-Khand Adducts: Trifluoromethyl as a Removable Steering Group (Angew. Chem. Int. Ed. 2…

2013

chemistry.chemical_compoundTrifluoromethylchemistryStereochemistryPauson–Khand reactionRegioselectivityCover (algebra)General ChemistrySteering groupCatalysisAdductAngewandte Chemie International Edition
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Ab Initio Study of Stereo- and Regioselectivity in the Diels−Alder Reaction between 2-Phenylcyclopentadiene and α-(Methylthio)acrylonitrile

1997

Ab initio molecular orbital calculations have been used to investigate the Diels−Alder reaction between 2-phenylcyclopentadiene and α-(methylthio)acrylonitrile. Geometry optimizations were performed with the RHF/3-21G, RHF/3-21G*, and RHF/6-31G* calculations while the correlation energy has been calculated at MP2 and MP3 levels. Four asynchronous transition structures corresponding to the formation of different stereoisomers and regioisomers associated with the four reaction channels have been located. The observed endo/exo stereoselectivity and para/meta regioselectivity are correctly described at all levels of calculation, and the calculated activation energies reflect accurately the rela…

chemistry.chemical_compoundchemistryComputational chemistryOrganic ChemistryAb initioStructural isomerRegioselectivityPhenyl groupStereoselectivityMolecular orbitalAcrylonitrileDiels–Alder reactionThe Journal of Organic Chemistry
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Photochemical Nitration by Tetranitromethane. Part XL. Regiochemistry of Trinitromethyl Attachment in the Photolysis of Benzofuran with Tetranitromet…

1997

chemistry.chemical_compoundchemistryGeneral Chemical EngineeringNitrationPhotodissociationRegioselectivityBenzofuranTetranitromethanePhotochemistryActa Chemica Scandinavica
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(3RS,1SR)-3-Bromo-3-(1-phenylpropyl)chroman-2,4-dione

2005

The title compound, C18H15BrO3, was obtained by bromination of phenprocoumone with N-bromo­succin­imide. The X-ray structure confirms an earlier proposal concerning the regioselectivity of the reaction to introduce the Br atom at the 3-position.

chemistry.chemical_compoundchemistryHalogenationRegioselectivityAtom (order theory)General Materials ScienceGeneral ChemistryCondensed Matter PhysicsImideMedicinal chemistryPhenprocoumoneActa Crystallographica Section E Structure Reports Online
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