Search results for "3-d"

showing 10 items of 1132 documents

Tryptophan catabolism via kynurenine production in Streptomyces coelicolor: identification of three genes coding for the enzymes of tryptophan to ant…

2011

Most enzymes involved in tryptophan catabolism via kynurenine formation are highly conserved in Prokaryotes and Eukaryotes. In humans, alterations of this pathway have been related to different pathologies mainly involving the central nervous system. In Bacteria, tryptophan and some of its derivates are important antibiotic precursors. Tryptophan degradation via kynurenine formation involves two different pathways: the eukaryotic kynurenine pathway, also recently found in some bacteria, and the tryptophan-to-anthranilate pathway, which is widespread in microorganisms. The latter produces anthranilate using three enzymes also involved in the kynurenine pathway: tryptophan 2,3-dioxygenase (TD…

chemistry.chemical_classificationKynurenine pathwayCatabolismHydrolasesStreptomyces coelicolorTryptophanTryptophanTryptophan Kynurenine S. coelicolor CDAStreptomyces coelicolorGeneral MedicineBiologybiology.organism_classificationApplied Microbiology and BiotechnologyTryptophan Oxygenasechemistry.chemical_compoundKynureninaseEnzymechemistryBiochemistryArylformamidaseIndoleamine 23-dioxygenaseKynurenineKynurenineMetabolic Networks and PathwaysBiotechnology
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Quantitative characterization of the global electrophilicity pattern of some reagents involved in 1,3-dipolar cycloaddition reactions

2003

Abstract The global electrophilicity power, ω, of a series of dipoles and dipolarophiles commonly used in 1,3-dipolar cycloadditions may be conveniently classified within a unique relative scale. The effects of chemical substitution on the electrophilicity of molecules have been evaluated using a representative set of electron-withdrawing and electron-releasing groups for a series of dipoles including nitrone, nitrile oxide and azide derivatives. The absolute scale of electrophilicity is used to rationalize the chemical reactivity of these species as compared to the static reactivity pattern of the reagents involved in the Diels–Alder reactions.

chemistry.chemical_classificationNitrileOrganic ChemistryPhotochemistryBiochemistryNitronechemistry.chemical_compoundchemistryComputational chemistryReagentDrug DiscoveryElectrophile13-Dipolar cycloadditionMoleculeReactivity (chemistry)AzideTetrahedron
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Understanding the origin of the asynchronicity in bond-formation in polar cycloaddition reactions. A DFT study of the 1,3-dipolar cycloaddition react…

2012

The origin of the asynchronicity in bond-formation in polar cycloadditions has been studied by an ELF analysis of the electron reorganisation along the 1,3-dipolar cycloaddition of Padwa's carbonyl ylide 4 with the 1,2-benzoquinone 8. This reaction presents an unexpected asynchronous bond-formation, which is initialised through the nucleophilic attack of Padwa's carbonyl ylide on the carbonyl oxygen atom of the strongly electrophilically activated 1,2-benzoquinone. The present study allows for the establishment that along an asynchronous bond-formation, the more favourable two-center interaction begins at the most electrophilic center, which is the center with the highest spin density achie…

chemistry.chemical_classificationNucleophileChemistryYlideGeneral Chemical EngineeringElectrophile13-Dipolar cycloadditionPolarGeneral ChemistrySpin densityBond formationPhotochemistryCycloadditionRSC Adv.
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A DFT study of the Huisgen 1,3-dipolar cycloaddition between hindered thiocarbonyl ylides and tetracyanoethylene

2004

Abstract The mechanism for the 1,3-dipolar cycloaddition between the hindered thiocarbonyl ylide 1 and tetracyanoethylene 2 has been studied at the B3LYP/6-31G ∗ level. Formation of the [3+2] cycloadduct 4 takes place through a stepwise mechanism that is initiated by the nucleophilic attack of the thiocarbonyl ylide 1 to the ethylene derivative 2 to give a zwitterionic intermediate IN . The subsequent cyclization of IN yields a seven-membered cyclic ketene imine 6 , which equilibrates with the thermodynamically more stable [3+2] cycloadduct 4 . The computed free energies are in agreement with the experimental outcomes.

chemistry.chemical_classificationOrganic ChemistryImineKeteneTetracyanoethylenePhotochemistryBiochemistryMedicinal chemistryCycloadditionchemistry.chemical_compoundchemistryNucleophileYlideDrug DiscoveryElectrophile13-Dipolar cycloadditionTetrahedron
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Supramolecular Nanocycles Comprisingβ-Cyclodextrin-click-Ferrocene Units: Rings of Rings of Rings

2010

We applied 1,3-dipolar cycloaddition to bind ethynylferrocene onto 6I-azido-6I-deoxycyclomaltoheptaose under microwave assisted conditions. The process was investigated by (1) H NMR, FT-IR spectroscopy, and MALDI-TOF mass spectrometry. The ability of the synthesized compound to self-organize to cyclic supramolecular structures was investigated by dynamic light scattering measurements and cryo-transmission electron microscopy.

chemistry.chemical_classificationPolymers and PlasticsCyclodextrinOrganic ChemistrySupramolecular chemistrymacromolecular substancesCycloadditionInclusion compoundchemistry.chemical_compoundchemistryFerrocenePolymer chemistry13-Dipolar cycloadditionMaterials ChemistryProton NMROrganic chemistryMetalloceneMacromolecular Rapid Communications
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Propane-1,3-diammonium molybdate

2019

The reaction between equimolar amounts of propane-1,3-diamine and molybdenum trioxide in water led to the formation of single crystals of the title salt, (C3H12N2)[MoO4]. The asymmetric unit is comprised of one propane-1,3-diammonium cation and one molybdate anion. The latter is isolated in the structure and has a slightly distorted tetrahedral configuration. An extensive network of N—H...O hydrogen bonds connects anions and cations, giving rise to a compact three-dimensional packing.

chemistry.chemical_classificationcrystal structure010405 organic chemistryHydrogen bondSalt (chemistry)General MedicineCrystal structureMolybdate010402 general chemistry01 natural sciences0104 chemical sciencesIonMolybdenum trioxidechemistry.chemical_compoundCrystallographychemistryPropanemolybdate saltpropane-13-diammoniumhydrogen bondslcsh:QD901-999[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM]Chemical Scienceslcsh:CrystallographyComputingMilieux_MISCELLANEOUS
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Co(II)-mediated synthesis of 2-carbamimidoylbenzoates and isoindole-1,3-diaminates

2015

Abstract Phthalonitrile, acetoxime and cobalt(II) nitrate hexahydrate are combined in acetone with formation of stable and easy to handle Co(II) complex [Co{C6H4C(NH2)NC(ONCMe2)2}2](NO3)2 (1). Interaction of 1 with excess alcohols ROH (also used as solvents) and 2 equiv of (NH4)2S leads, in one-step, to alkyl 2-carbamimidoylbenzoate nitrates [C6H4COOR{2-C(NH2)2}]NO3 [R=CH3, C2H5, C3H7, CH(CH3)2]. Similarly, N1,N3-dialkyl-1H-isoindole-1,3-diaminate nitrates [C6H4C(NR′)NC(NR′)]NO3 [R=C3H7, C4H9, C(CH3)3, CH2CH2OH, CH2CH2SC2H5) can be directly produced from 1 by its reaction with 4 equiv of amines and 2 equiv of (NH4)2S in alcoholic media.

chemistry.chemical_classificationphthalonitrilesChemistryStereochemistrymetal assisted (mediated) synthesisOrganic Chemistrychemistry.chemical_elementN1oximesBiochemistryMedicinal chemistryPhthalonitrilechemistry.chemical_compoundNitrateDrug DiscoveryAcetone3-diaminatesIsoindoleCobaltta116alkyl 2-carbamimidoylbenzoatesN3-dialkyl-isoindole-1AlkylTetrahedron
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Understanding the kinetic solvent effects on the 1,3-dipolar cycloaddition of benzonitrile N-oxide: a DFT study

2011

JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, ISSN : 0894-3230, DOI : 10.1002/poc.1858, Issue : 7, Volume : 24, pp. 611 – 618, JUILLET 2011.

chemistry.chemical_compoundBenzonitrilechemistryVolume (thermodynamics)Computational chemistryOrganic Chemistry13-Dipolar cycloadditionPhysical organic chemistryOxideDensity functional theoryPhysical and Theoretical ChemistrySolvent effectsElectron localization functionJournal of Physical Organic Chemistry
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Electrosynthesis of Stable Betulin‐Derived Nitrile Oxides and their Application in Synthesis of Cytostatic Lupane‐Type Triterpenoid‐Isoxazole Conjuga…

2021

chemistry.chemical_compoundBetulinTriterpenoidchemistryNitrileOrganic Chemistry13-Dipolar cycloadditionOrganic chemistryPhysical and Theoretical ChemistryIsoxazoleElectrosynthesisLupeolConjugateEuropean Journal of Organic Chemistry
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Theoretical Study of the 1,3-Dipolar Cycloaddition Reactions of Azomethine Ylides. A DFT Study of Reaction between Trifluoromethyl Thiomethyl Azometh…

1999

The molecular mechanism for the 1,3-dipolar cycloaddition of trifluoromethyl thiomethyl azomethine ylide with acronitrile has been characterized using density functional theory methods with the B3L...

chemistry.chemical_compoundTrifluoromethylchemistryComputational chemistryOrganic Chemistry13-Dipolar cycloadditionMolecular mechanismAzomethine ylideDensity functional theoryCycloadditionThe Journal of Organic Chemistry
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