Search results for "Heteroatom"

showing 10 items of 63 documents

Table of periodic properties of human immunodeficiency virus inhibitors

2010

Classification algorithms are proposed based on information entropy. The feasibility of mixing a given human immunodeficiency virus (HIV) inhibitor with dissimilar ones is studied. The 31 inhibitors are classified by their structural chemical properties. Many classification algorithms are based on information entropy. An excessive number of results appear compatible with the data and suffer combinatorial explosion. However, after the equipartition conjecture one has a selection criterion. According to this conjecture, the best configuration is that in which entropy production is most uniformly distributed. The structural elements of an inhibitor can be ranked according to their inhibitory a…

CombinatoricsStatistical classificationMathematical optimizationConjectureDocking (molecular)Entropy productionHeteroatomPrincipal component analysisHuman immunodeficiency virus (HIV)medicinemedicine.disease_causeCombinatorial explosionMathematicsInternational Journal of Computational Intelligence in Bioinformatics and Systems Biology
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Eight-membered Rings with Two Heteroatoms 1,5

2008

The chapter of the third edition of Comprehensive Heterocyclic Chemistry (CHEC III) 12.24 titled ‘Eight-membered Rings with two Heteroatoms 1,5’ deals with diheterocines rings with two heteroatoms in a 1,5 relationship, namely 1,5-diazocine, 1,5-oxazocine, 1,5-thiazocine, 1,5-dioxocin, 1,5-oxathiocin, and 1,5-dithiocin. This chapter covers the literature from 1996 to 2006 and also reports those articles published in 1995 which were not reported in CHEC-II(1996). In this edition, in addition to the uncondensed derivatives, eight-membered 1,5-heterocycles fused to five-, six-, and seven-membered carbocycles or heterocycles are covered. Bridged diheterocines, which actually constitute the majo…

CombinatoricsTheoretical methodsHeteroatomSingle classBispidinone
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Recent Advances in Catalytic Enantioselective Synthesis of Pyrazolones with a Tetrasubstituted Stereogenic Center at the 4-Position

2020

AbstractPyrazolone [2,4-dihydro-3H-pyrazol-4-one] represents one of the most important five-membered nitrogen heterocycles which is present in numerous pharmaceutical drugs and molecules with biological activity. Recently, many catalytic methodologies for the asymmetric synthesis of chiral pyrazolones have been established with great success, specially, for the synthesis of pyrazolones bearing a tetrasubstituted stereocenter at C-4. This review summarizes these excellent research studies since 2018, including representative examples and some mechanistic pathways explaining the observed stereochemistry.1 Introduction2 Catalytic Enantioselective Synthesis of Chiral Pyrazolones with a Full Car…

Compostos heterocíclicsChemistryOrganic ChemistryHeteroatomPyrazoloneEnantioselective synthesisCombinatorial chemistryCatalysisStereocenterCatalysisCompostos de nitrogenCatàlisiOrganocatalysismedicineResearch studiesPyrazolonesmedicine.drug
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C−C Cross-Couplings from a Cyclometalated Au(III) C∧ N Complex: Mechanistic Insights and Synthetic Developments

2021

Abstract In recent years, the reactivity of gold complexes was shown to extend well beyond π‐activation and to hold promises to achieve selective cross‐couplings in several C−C and C−E (E=heteroatom) bond forming reactions. Here, with the aim of exploiting new organometallic species for cross‐coupling reactions, we report on the Au(III)‐mediated C(sp2)−C(sp) occurring upon reaction of the cyclometalated complex [Au(CCH2N)Cl2] (1, CCH2N=2‐benzylpyridine) with AgPhCC. The reaction progress has been monitored by NMR spectroscopy, demonstrating the involvement of a number of key intermediates, whose structures have been unambiguously ascertained through 1D and 2D NMR analyses (1H, 13C, 1H‐1H CO…

Coordination sphereHeteroatom010402 general chemistry01 natural sciencesCatalysisReductive eliminationNMR spectroscopyNucleophilecross-couplingReactivity (chemistry)Full Paper010405 organic chemistryChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryOrganic Chemistryreductive eliminationGeneral ChemistryNuclear magnetic resonance spectroscopy[CHIM.CATA]Chemical Sciences/CatalysisFull PapersTransition state0104 chemical sciencesgold cyclometalated complexesCrystallographyZincSettore CHIM/03 - Chimica Generale E InorganicaGoldTwo-dimensional nuclear magnetic resonance spectroscopyorganometallics
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A DFT study of the Karplus-type dependence of vicinal 3J(Sn-C-X- C), X=N,O,S, in organotin(iv) compounds: Application to conformationally flexible sy…

2010

ZORA relativistic and non-relativistic DFT protocols have been used to investigate vicinal coupling constants, (3)J(Sn-C-X-C), in several organotin(iv) compounds, with particular emphasis on cyclic alpha-aminoorganostannanes. The dependence of the coupling constant on the heteroatom X (X = N,O,S) in the coupling path, and, for X = N, its substituents, has been studied in detail. The electron-withdrawing strength of the N-substituents has been found to strongly affect the magnitude and shape of the Karplus-type curve. The results obtained for the simple model systems, having no or little conformational flexibility, have helped in rationalizing the data concerning real flexible cyclic systems…

Coupling constantCouplingeducation.field_of_study119Tin NMR vicinal coupling constants DFTChemistryOrganic ChemistryHeteroatomPopulationType (model theory)BiochemistryComputational chemistryPhysical and Theoretical ChemistryeducationConformational isomerismVicinal
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Fluorinated Heterocyclic Compounds− The First Example of an Irreversible Ring-Degenerate Rearrangement on Five-Membered Heterocycles by Attack of an …

2004

The reactions of 5-perfluoroalkyl-1,2,4-oxadiazoles 3 with hydroxylamine in DMF give the regioisomeric 3-perfluoroalkyl-1,2,4-oxadiazoles 4 in excellent yields. This process is the first example of ring-degenerate rearrangement (RDR) occurring on five-membered heterocycles by attack of an external bidentate nucleophile, which replaces two heteroatoms of the ring. We suggest that an ANRORC-like mechanism occurs in which the addition of the nucleophilic nitrogen atom (NH2OH) on the C(5) atom of 3 is followed by ring opening and irreversible ring-degenerate closure by attack of the nucleophilic oxygen atom (=NOH) on the C(3) atom of the original ring, realizing an elegant and efficient synthes…

DenticityStereochemistryrearrangementOrganic ChemistryHeteroatomDegenerate energy levelsAtom (order theory)General MedicineRing (chemistry)Medicinal chemistrychemistry.chemical_compoundHydroxylaminechemistryNucleophilering-ring interconversionNucleophilic substitutionAb initio computationsnucleophilic substitutionPhysical and Theoretical ChemistryheterocycleEuropean Journal of Organic Chemistry
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Eight-membered heterocycles with two heteroatoms in a 1,2-relationship of interest in medicinal chemistry

2021

Abstract This chapter treats 1,2-diheterocines, eight membered heterocyclic systems with two heteroatoms, N, O and S, in an 1,2 relationship, exhibiting biological properties and exhaustively covers the literature from 2007 to the end of November 2019. In this period of time 1,2-diazocine, 1,2-oxazocine, 1,2-dioxocin and 1,5-dithiocin ring systems had derivatives exhibiting pharmacological activities. No articles on biological properties have been reported for 1,2-thiazocines and 1,2-oxathiocins. Besides uncondensed derivatives, 1,2-diheterocines fused with five-, six-, and seven-membered carbocycles or heterocycles have been reviewed, as well as bridged 1,2-diheterocines.

Eight-membered heterocycles with two heteroatoms 12 Medicinal chemistry Biological activity 12-Diazocines 12-Oxazocines 12-Dioxocins 12-DithiocinsChemistryBiological propertyHeteroatomOrganic chemistryRing (chemistry)
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CO2 turned into a nitrogen doped carbon catalyst for fuel cells and metal–air battery applications

2021

Heteroatom doped metal-free catalysts are one of the most promising replacements for platinum for the alkaline oxygen reduction reaction (ORR). Due to the lack of metal atoms, they are extremely stable and environmentally friendly. However, production of carbon nanomaterials can have a very high CO2 footprint. In this study, we present ORR catalysts made directly from CO2via molten salt CO2 electrolysis. The deposited carbon powder is doped with nitrogen using pyrolysis in the presence of dicyandiamide. The effect of molten carbonate electrolyte composition towards the final ORR activity in 0.1 M KOH is studied. A thorough physico-chemical study of the starting carbons and N-doped catalysts…

ElectrolysisMaterials scienceHeteroatomchemistry.chemical_elementPollutionCatalysislaw.inventionchemistryChemical engineeringlawEnvironmental ChemistryRotating disk electrodeMolten saltPlatinumCarbonBET theoryGreen Chemistry
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Xylochemical Synthesis of Cytotoxic 2-Aminophenoxazinone-Type Natural Products Through Oxidative Cross Coupling

2019

Today, the total synthesis of natural products mostly relies on the use of petroleum-based starting materials. The commercial availability of building blocks of this type often deflects attention away from lengthy synthetic routes required for the reintroduction of heteroatom substitution patterns lost in the geological process of kerogenesis. Herein, the use of wood-based starting materials, the so-called xylochemicals, for the synthesis of 2-aminophenoxazinone natural products is presented. The inherent heteroatom substitution patterns as well as chemical functionalities were employed and permitted a short and straightforward synthetic strategy. Moreover, a novel and “green” method for co…

Geological processChemical substanceRenewable Energy Sustainability and the EnvironmentChemistryGeneral Chemical EngineeringSubstitution (logic)HeteroatomTotal synthesis02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesCombinatorial chemistryNatural (archaeology)0104 chemical sciencesEnvironmental ChemistryMoiety0210 nano-technologyACS Sustainable Chemistry & Engineering
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Silver Ion-Selective Electrodes Based on π-Coordinating Ionophores Without Heteroatoms

2002

Ion-selective electrodes (ISEs) were constructed by using spherical hydrocarbons (cyclophanes) as π-coordinating ionophores in solvent polymeric membranes. Four structurally similar cyclophanes, i. e., [2.2.2]p,p,p-cyclophane, [2.2.2]m,p,p-cyclophane, [2.2.1]p,p,p-cyclophane and [2.2.1]m,p,p-cyclophane were studied as ionophores for Ag+. The ion-selective membranes were composed of the corresponding ionophore (1%), potassium tetrakis(4-chlorophenyl)borate (0.5%), 2-nitrophenyl octyl ether (65–66%) and PVC (32–33%). The ion-selective membrane was placed on top of a layer of the conducting polymer, poly(3,4-ethylenedioxythiophene) (PEDOT), working as ion-to-electron transducer. The selectivit…

HeteroatomInorganic chemistryIonophoreEtherAnalytical ChemistryIon selective electrodeSolventchemistry.chemical_compoundMembranechemistryPolymer chemistryElectrochemistrySelectivityCyclophaneElectroanalysis
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