Search results for "pyridine derivative"

showing 5 items of 5 documents

A green and efficient method for the synthesis of homodimeric (β-dicarbonyl) arylmethanes and dihydropyridine from dimedone in water

2018

A direct method has been developed for the synthesis of the dihydropyridine ring system by means of Michael reaction. The reaction of dimedone with 1 .0 equiv. of amines in water provides intermediate product, which allowed dihydropyridine derivatives by intramolecular cyclization in various yields. Of particular interest is the use of the water as solvent of reaction and in absence of catalyst. Also these operating conditions protect the environment and economic points of view.Keywords: aqueous synthesis; bioactivity; dihydropyridine; dimedone; green method; selective conditions

010405 organic chemistryChemistryDihydropyridine010402 general chemistry01 natural sciencesaqueous synthesis; bioactivity; dihydropyridine; dimedone; green method; selective conditionsIntermediate product0104 chemical sciencesCatalysisSolventchemistry.chemical_compoundDimedoneIntramolecular forcemedicineMichael reactionOrganic chemistryDihydropyridine derivativesmedicine.drugJournal of Fundamental and Applied Sciences
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Synthesis of Pyrrolo-Condensed Derivatives with Potential Antiviral Activity

2014

NITROPHENYL-1H-PYRROLO[23-c]PYRIDINE DERIVATIVESAntiviral ActivitySettore CHIM/08 - Chimica FarmaceuticaBromopyridinethyilthioureaisoindolo[21-a]quinoxaline
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Distinct photodynamics of κ-N and κ-C pseudoisomeric iron(ii) complexes

2021

Two closely related FeII complexes with 2,6-bis(1-ethyl-1H-1,2,3-triazol-4yl)pyridine and 2,6-bis(1,2,3-triazol-5-ylidene)pyridine ligands are presented to gain new insights into the photophysics of bis(tridentate) iron(II) complexes. The [Fe(N^N^N)2]2+ pseudoisomer sensitizes singlet oxygen through a MC state with nanosecond lifetime after MLCT excitation, while the bis(tridentate) [Fe(C^N^C)2]2+ pseudoisomer possesses a similar 3MLCT lifetime as the tris(bidentate) [Fe(C^C)2(N^N)]2+ complexes with four mesoionic carbenes. Financial support from the Deutsche Forschungsge-meinschaft [DFG, Priority Program SPP 2102] "Light-controlled reactivity of metal complexes" (BA 4467/7-1, LO 714/11-1, …

TrisDenticitysynthesisPyridinepyridine derivativecarbenoidIron compoundsCatalysisexperimental studychemistry.chemical_compoundPyridineMaterials Chemistryphysical chemistrycontrolled studyChemistrySinglet oxygenPyridine ligandsSinglet oxygenMetals and AlloysMesoionicGeneral ChemistryNanosecondPyridine ligandSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialsunclassified drugCrystallographyPhotophysicsiron complexisomerCeramics and CompositesCarbeneschemical structurephotodynamicsphysicsExcitationchemical parameters
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Crystal structure of (E)-4-[N-(7-methyl-2-phenyl-imidazo[1,2-a]pyridin-3-yl)carboximido-yl]phenol.

2015

The molecule of the title compound, C21H17N3O, is built up from fused five- and six-membered rings connected to a methyl group, a phenyl ring and an (iminomethyl)phenol group. The fused ring system is almost planar (r.m.s. deviation = 0.031 Å) and forms dihedral angles of 64.97 (7) and 18.52 (6)° with the phenyl ring and the (iminomethyl)phenol group, respectively. In the crystal, centrosymmetric molecules are linked by pairs of C—H...π interactions into dimeric units, which are further connected by O–H...N hydrogen bonds to form layers parallel to (101).

crystal structureCrystallographyHydrogen bondimidazo[12a]pyridine derivativeGeneral ChemistryCrystal structureDihedral angleCondensed Matter PhysicsRing (chemistry)Bioinformaticshydrogen bondingC—H⋯π inter­actionsMedicinal chemistryData ReportsCrystalchemistry.chemical_compoundC—H...π interactionschemistryQD901-999Group (periodic table)PhenolGeneral Materials ScienceMethyl groupActa crystallographica. Section E, Crystallographic communications
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Unexpected behaviour of copper(I) towards a tridentate Schiff base: Synthesis, structure and properties of new Cu(I)-Cu(II) and Cu(II) complexes

2001

cited By 17; International audience; The reaction of CuBr with 2,6-bis[1-(2,6-diisopropylphenylimino)ethyl]pyridine L afforded a new Cu(I)-Cu(II) derivative [CuBrL]2[Cu2Br4] (1), while the reaction of [Cu(CH3CN)4]PF6 with L in THF yielded the new Cu(I) compound CuL(THF)(CH3CN)PF6 (2). Derivative 2 further reacted with halogenated solvents to yield halogeno-Cu(II) salts, [CuClL]PF6 (3) using CHCl3 and [CuBrL]Br3 (4) using CHBr3. Compounds 1, 3 and 4 have been fully characterised by X-ray crystallography; they contain essentially similar [CuXL]+ cations with a square planar copper(II) co-ordination. However, the structure of compound 1 must be viewed as built of tetranuclear units since two […

crystal structurespectroscopysynthesisStereochemistry2chemistry.chemical_elementcyclic potentiometrypyridine derivativeCrystal structure010402 general chemistryElectrochemistry01 natural sciencesMedicinal chemistrysolventIonInorganic Chemistrychemistry.chemical_compoundSchiff basecopper derivativehalogenationPyridineMaterials Chemistry[CHIM]Chemical SciencesPhysical and Theoretical Chemistrychemical bondSchiff base010405 organic chemistryChemistry6 bis[2chemical interactionarticleanionX ray crystallographyCopperstructure analysis0104 chemical sciencescationunclassified drug6 diisopropylphenylimino)ethyl]pyridineelectrochemistryYield (chemistry)magnetismDerivative (chemistry)copper bromide
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