Search results for "medicinal"

showing 10 items of 2966 documents

Heterocyclic rearrangements. Phenylhydrazones andN-methyl-N-phenylhydrazones of 3-acylisoxazoles

1983

The reaction of 3-benzoyl-5-phenylisoxazole (4) and 3-acetyl-5-methylisoxazole (5) with phenylhydrazine and N-methyl-N-phenylhydrazine has been investigated and the reactivity of (E)- and (Z)-phenylhydrazones and N-methyl-N-phenylhydrazones has been studied.

chemistry.chemical_compoundChemistryOrganic ChemistryTriazole derivativesReactivity (chemistry)Medicinal chemistryPhenylhydrazineJournal of Heterocyclic Chemistry
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ChemInform Abstract: Heterocyclic Photorearrangements. Photoinduced Rearrangement of 3-Styryl-1,2,4-oxadiazoles.

1990

The photochemical behaviour of 3-styryl-5-phenyl-(5-methyl)-1,2,4-oxadiazoles in methanol at 254 nm has been investigated. A photoinduced rearrangement to the quinoline system has been pointed out and explained as proceeding through an initial photolysis of the ring ON bond, followed by a six membered ring closure reaction involving the styryl moiety.

chemistry.chemical_compoundChemistryPhotodissociationQuinolineClosure (topology)MoietyGeneral MedicineMethanolRing (chemistry)Medicinal chemistryChemInform
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Synthese von Oligo(p-phenylen-m-pyridindiyl)en

2000

chemistry.chemical_compoundChemistryPyridineCross-conjugationMedicinal chemistryJournal für praktische Chemie
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ChemInform Abstract: Highly Enantio- and Diastereoselective Inverse Electron Demand Hetero-Diels-Alder Reaction Using 2-Alkenoylpyridine N-Oxides as …

2009

A general catalytic inverse electron demand hetero-Diels Alder reaction for 2-alkenoylpyridine N-oxides is presented. 2-Alkenoylpyridine N-oxides react very efficiently with alkenes in the presence of bisoxazolidine-copper(II) [BOX-Cu(II)] complexes to give chiral dihydropyrans bearing a pyridine ring at the 6-position with very high yields and excellent diastereo- and enantioselectivity. These heterodienes exhibited higher reactivity and enantioselectivity than the corresponding non-oxidized 2-alkenoylpyridines.

chemistry.chemical_compoundChemistryPyridineInverseReactivity (chemistry)General MedicineElectronRing (chemistry)Medicinal chemistryCatalysisDiels–Alder reactionChemInform
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Phosphororganische Verbindungen. 611. Polarographische Untersuchung quartärer Phosphonium- und Arsoniumsalze

1969

Summary The half-wave potentials of a number of quaternary phosphonium and arsonium salts are determined under standard conditions, and their dependence on the concentration of the substrate, the temperature, the drop rate, the height of the mercury head, and the concentration of the capillary-active substance (Triton X-100) is established. It is not possible to deduce from the half-wave potentials which ligands, and in what proportion these ligands, are reductively cleaved. The results suggest that ligands are split off as radicals (transfer, of one electron) and as anions (transfer of two electrons).

chemistry.chemical_compoundChemistryRadicalInorganic chemistrychemistry.chemical_elementElectronPhosphoniumMedicinal chemistryMercury (element)Journal of Electroanalytical Chemistry and Interfacial Electrochemistry
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ChemInform Abstract: Palladium-Catalyzed Suzuki Carbonylative Reaction of α-Halomethyl Oxime Ethers: A Regioselective Route to Unsymmetrical 1,3-Oxyi…

2015

chemistry.chemical_compoundChemistryRegioselectivitychemistry.chemical_elementGeneral MedicineOximeMedicinal chemistryPalladiumCatalysisChemInform
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Synthesis of pillar[7]arene

2012

Abstract The first synthesis of pillar[7]arene is reported with two methods. Method A: the FeCl 3 -catalyzed condensation reaction of 1,4-dimethoxybenzene ( 1 ) with paraformaldehyde in CHCl 3 gave dimethoxypillar[7]arene ( 3 ). Method B: the p -toluenesulfonic acid catalyzed condensation reaction of 2,5-bis(benzyloxymethyl)-1,4-dimethoxybenzene ( 2 ) in CH 2 Cl 2 gave compound 3 . Demethylation of 3 with BBr 3 gave pillar[7]arene ( 4 ). The pillar[7]arene might be a perspective macrocyclic host in host–guest chemistry.

chemistry.chemical_compoundChemistryStereochemistryAcid catalyzedPillarGeneral ChemistryParaformaldehydeCondensation reactionMedicinal chemistryDemethylationCatalysisChinese Chemical Letters
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Scandium-catalyzed preparation of cytotoxic 3-functionalized quinolin-2-ones: Regioselective ring enlargement of isatins or imino isatins

2012

Trimethylsilyldiazomethane in the presence of catalytic amounts of Sc(OTf) 3 smoothly promotes the ring expansion of isatins or imino isatins to efficiently afford 3-functionalized quinolin-2-ones through controlled ring enlargement. Whereas the ring-expansion reaction of azetidine-2,3-diones led to the adduct resulting from migration of the carbonyl group, the ring-expansion reaction of oxindole derivatives gave the adduct resulting from migration of the aryl group. To rationalize the experimental observations, theoretical studies have been performed. Moreover, the biological activity of some of the synthesized heterocycles has been evaluated in four cancer cell lines. © 2012 Wiley-VCH Ver…

chemistry.chemical_compoundChemistryStereochemistryArylRegioselectivityHomogeneous catalysisOxindoleGeneral ChemistryTrimethylsilyldiazomethaneRing (chemistry)Medicinal chemistryAdductCatalysis
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ChemInform Abstract: Synthesis and Spectroscopic Characterizations of Both 1-Ethyl-4,8- dihydro-10-methoxy-3-methyl-8-R1-6-R2-dipyrazolo(3,4-b:4′,3′-…

2010

The non-selective methylation of compounds 3a-d using ethereal diazomethane, allowed the synthesis of isomers 4 and 5 which were useful intermediates for the preparation, by a simple approach, of the title compounds 7 and 9. A complete assignment of the chemical shifts to the carbon atoms of the compounds 7 and 9 was performed by different nmr experiments, such as DEPT and XHDEPT for onebond CH correlations and COLOC experiments for long-range C-H correlations.

chemistry.chemical_compoundChemistryStereochemistryDiazomethaneChemical shiftchemistry.chemical_elementGeneral MedicineMethylationDEPTCarbonMedicinal chemistryChemInform
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ChemInform Abstract: Synthesis of Highly Fluorinated 2,2′-Biphenols and 2,2′-Bisanisoles.

2011

The selective Ullmann-type reaction proceeds under solvent-free conditions and tolerates even a bromo substituent.

chemistry.chemical_compoundChemistrySubstituentGeneral MedicineMedicinal chemistryChemInform
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