Search results for "DERIVATIVES"

showing 10 items of 432 documents

ChemInform Abstract: A Versatile Palladium/Triphosphane System for Direct Arylation of Heteroarenes with Chloroarenes at Low Catalyst Loading.

2010

The present new catalyst system can be used for the direct arylation of various heteroaromatic compounds at low palladium loadings.

chemistry.chemical_compoundTriphosphanechemistrychemistry.chemical_elementGeneral MedicineCombinatorial chemistryThiophene derivativesPyrrole derivativesCatalysisPalladiumChemInform
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Application of Molecular Topology to the Prediction of the Reaction Yield and Anticancer Activity of Imidazole and Guanidine Derivatives

2013

In this study molecular topology based QSAR has been applied to predict the reaction yield and anticancer activity of 18 imidazole and guanidine derivatives. Four properties were evaluated, namely reaction yield, anti prostatic-cancer activity, anti breast-cancer activity and anti lung-cancer activity. The four models have been validated by both internal and cross validation, and also by randomness tests. The results obtained are in full agreement with the experimental results and confirm the precision, accuracy and robustness of the method followed. After carrying out a virtual screening upon such models, new imidazole and guanidine derivatives with potential anticancer activity are propos…

chemistry.chemical_compoundVirtual screeningQuantitative structure–activity relationshipchemistryStereochemistryImidazoleMultiple linear regression analysisMolecular topologyCombinatorial chemistryGuanidine derivativesInternational Journal of Chemoinformatics and Chemical Engineering
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ChemInform Abstract: Water-Soluble Palladium Nanoparticles: Click Synthesis and Applications as a Recyclable Catalyst in Suzuki Cross-Couplings in Aq…

2011

Polyethylene glycol-tagged macrocycle (I) is prepared by a three-fold copper-catalyzed [3 + 2] cycloaddition reaction.

chemistry.chemical_compoundWater solubleAqueous mediumChemistryPolymer chemistryPalladium nanoparticlesGeneral MedicinePolyethyleneThiophene derivativesRecyclable catalystCycloadditionChemInform
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From One-Pot NH-Sulfoximidations of Thiophene Derivatives to Dithienylethene-Type Photoswitches

2019

Thiophene NH-sulfoximines have been synthesized using a one-pot NH-sulfoximidation reaction of thiophenes. The reactivity of the products was investigated, and the developed protocols were used for the synthesis of a new class of dithienylethene-type photoswitches containing a sulfoximidoyl group.

chemistry.chemical_compoundchemistry010405 organic chemistryOrganic ChemistryThiopheneOrganic chemistryReactivity (chemistry)Physical and Theoretical Chemistry010402 general chemistry01 natural sciencesBiochemistryThiophene derivatives0104 chemical sciencesOrganic Letters
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ChemInform Abstract: Total Synthesis of (-)-Hymenosetin.

2016

Hymenosetin (I) and its N-methyl analogue are prepared in 11 and 8 steps, respectively, from citronellal employing an intramolecular Diels-Alder reaction as the key step.

chemistry.chemical_compoundchemistryIntramolecular forcefungiCitronellalHymenosetinOrganic chemistryTotal synthesisGeneral MedicinePyrrole derivativesChemInform
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ChemInform Abstract: Modular One-Pot Synthesis of Tetrasubstituted Pyrroles from α-(Alkylideneamino)nitriles.

2008

2,3,4,5-Tetrasubstituted pyrroles have been prepared with high regioselectivity by a formal cycloaddition of α-(alkylideneamino)nitriles and nitroolefins followed by elimination of HCN and HNO2. The reaction allows the convergent construction of the pyrrole ring in four steps from a nitroalkane and three aldehydes.

chemistry.chemical_compoundchemistryOne-pot synthesisOrganic chemistryRegioselectivityNitroalkaneGeneral MedicineRing (chemistry)Combinatorial chemistryCycloadditionPyrrole derivativesPyrroleChemInform
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Design of guanidinium porphyrins as potential G-quadruplex ligands

2012

We report herein an easy and smooth synthesis of two novel tetra-meso-substituted porphyrins bearing terminal guanidinium functionalities. These two guanidine derivatives are the porphyrin-based analogs of ZnPC , a closely related phthalocyanine-based molecule with four guanidinium arms already reported as an efficient G-quadruplex ligand.

chemistry.chemical_compoundchemistryStereochemistryLigandPhthalocyanineMoleculeGeneral ChemistryG-quadruplexPorphyrinGuanidine derivativesJournal of Porphyrins and Phthalocyanines
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The reaction of amino-imidazoles, -pyrazoles and -triazoles with α,β-unsaturated nitriles

2005

The reactions of α,β-unsaturated nitriles (1, 9, 12) as bielectrophiles with aminoazoles (2, 4, 6) as binu-cleophiles were investigated. Acrylonitrile (1) reacts almost exclusively in a chemoselective Michael-type addition yielding the substituted azoles 3, 5 and 7, respectively. Cinnamonitriles 9a,b behave in a similar way, but the free CN group adds a second molecule 4 yielding 10a,b and its cyclocondensation product 11a,b as minor component. The attempted formation of azolopyrimidines is best achieved by the reaction of the benzylidenemalononitriles 12a - f with 2 or 4. The process is chemo- and regioselective. The structure determinations were based on NMR measurements including DEFT, C…

chemistry.chemical_compoundchemistryStereochemistryOrganic ChemistryTriazole derivativesRegioselectivityMoleculeGeneral MedicineCN-groupAcrylonitrileMedicinal chemistryJournal of Heterocyclic Chemistry
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ChemInform Abstract: 1,2,4-Oxadiazole Rearrangements Involving an NNC Side-Chain Sequence.

2010

The thermal rearrangement of N-1,2,4-oxadiazol-3-yl-hydrazones into 1,2,4-triazole derivatives is reported. This represents the first example of a three-atom side-chain rearrangement involving an NNC sequence linked at the C(3) of the oxadiazole. The reactions carried out under solvent-free conditions produced good to high yields of the final products.

chemistry.chemical_compoundchemistryStereochemistryTriazole derivativesSide chainOxadiazoleGeneral MedicineSequence (medicine)ChemInform
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ChemInform Abstract: Facile Synthesis of Pyrazoles and Pyrroles via Thermolysis of Tetrazolo[1,5-b]pyridazines, Tetrazolo[1,5-a]pyrimidines and Tetra…

2010

Abstract A simple and high yielding preparation of pyrazoles and pyrroles is described. Thermolysis of tetrazolo[1,5- b ]pyridazines, tetrazolo[1,5- a ]pyrimidines and tetrazolo[1,5- a ]pyridines allowed easy ring contraction thus providing a facile preparation of cyanopyrazole and cyanopyrrole heterocycles. Since the cyano group is a versatile precursor of other functionalities, the reaction appears of particular interest for the construction of a variety of pyrazoles and pyrroles. The simple preparation of the starting tetrazole derivatives, the relatively mild conditions employed, and the very short reaction times make this versatile procedure of great synthetic utility and applicable bo…

chemistry.chemical_compoundchemistryThermal decompositionTetrazoleGeneral MedicineRing (chemistry)High yieldingCombinatorial chemistryPyrrole derivativesChemInform
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