Search results for "HILIC"

showing 10 items of 745 documents

Covalent and non-covalent chemistry of 2D black phosphorus

2021

The post-graphene era is undoubtedly marked by two-dimensional (2D) sheet polymers, such as black phosphorus (BP). This emerging material has a fascinating structure and outstanding electronic properties and has been postulated for a plethora of applications. The need to circumvent the pronounced oxophilicity of P atoms has dominated the research on this material in recent years, with the objective of finding the most effective method to improve its environmental stability. When it comes to chemical functionalization, the few approaches reported so far involve some drawbacks such as low degree of addition and low production ability. This review presents the concepts and strategies of our st…

ChemistryGeneral Chemical EngineeringNon covalentNanotechnology02 engineering and technologyGeneral ChemistryQuímica010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesBlack phosphorus0104 chemical sciencesCharacterization (materials science)ChemistryCovalent bondChemical functionalizationOxophilicityBasal plane0210 nano-technologyMaterialsElectronic propertiesddc:547
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Electrophilic Aromatic Substitution. VonR. Taylor. Wiley, Chichester 1990. XVI, 513 S., geb. £ 85.00 — ISBN 0-471-92482-2

1991

ChemistryGeneral MedicineElectrophilic aromatic substitutionMedicinal chemistryAngewandte Chemie
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Calculations on solvents and co-solvents of single-wall carbon nanotubes:cyclopyranoses

2005

The (10, 10) single-wall carbon nanotube (SWNT) presents consistency between relatively small solubility, and large partition coefficients and kinetic stability. The solubility of SWNTs is investigated in a variety of solvents, finding a class of non-hydrogen-bonding Lewis bases that provides good solubility. The organic solvent–water partition and hydrophobic moment of lysozyme show that the main contribution to the water-accessible surface area of helices is the hydrophobic term, while the hydrophilic part dominates in the sheet, which is related to the 1-octanol–, cyclohexane– and chloroform–water partition coefficients Po−ch−cf of helices, which are greater than those of the sheet. The …

ChemistryMechanical EngineeringBioengineeringGeneral ChemistryCarbon nanotubeKinetic energylaw.inventionPartition coefficientChemical engineeringMechanics of MaterialslawLipophilicityOrganic chemistryPartition (number theory)General Materials ScienceLewis acids and basesElectrical and Electronic EngineeringSolubilityCo solventNanotechnology
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Book Review: Electrophilic Aromatic Substitution. By R. Taylor

1991

ChemistryOrganic chemistryGeneral MedicineGeneral ChemistryElectrophilic aromatic substitutionCatalysisAngewandte Chemie International Edition in English
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Organometallic nucleophiles. Mechanism of halide displacement at saturated carbon by 2-pyridyl and 4-Pyridyl complexes [M(dmtc)(C5H4N-Cn)(L)] (M  Pd…

1992

Abstract A mechanistic study is reported of nucleophilic halide substitution by pyridyl complexes [M(dmtc)C 5 H 4 N- C 2 )(L)] (M  Pd or Pt; L  PMe 3 , PEt 3 or PPh 3 ) and [Pd(dmtc)C 5 H 4 N- C 4 )(L)] (L  PMe 3 or PPh 3 ) on organic halides XCH 2 R (X  Cl or Br; R  CHCH 2 , COMe, Ph, or CN) in various solvents, yielding the pyridylium derivatives [M(dmtc)1-CH 2 R)C 5 H 4 N- C 2 (L)] + and [Pd(dmtc)(1-CH 2 R)(C 5 H 4 N- C 4 (L)] + , respectively. The kinetics obey a second-order rate law: rate  k 2 [XCH 2 R][Complex]. A similar rate law is observed for the analogous reactions involving 4-dimethyl-aminopyridine (4-dmapy) as the nucleophile. The effects of solvent and leaving group, a…

ChemistryStereochemistryOrganic ChemistrySubstituentLeaving groupHalideBiochemistryMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundReaction rate constantNucleophilePyridineMaterials ChemistryNucleophilic substitutionPhysical and Theoretical ChemistrySolvent effectsJournal of Organometallic Chemistry
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High Yield SNAr on 8-Halogenophenyl-BODIPY with Cyclic and Acyclic Polyamines

2014

Selective nucleophilic aromatic substitutions with several polyamines were performed in very good yields on halogeno-phenyl BODIPY derivatives containing an activating nitro group.

ChemistryStereochemistryOrganic Chemistrymacromolecular substancesFluorescenceMedicinal chemistrychemistry.chemical_compoundNucleophileNucleophilic aromatic substitutionYield (chemistry)Nucleophilic substitutionNitroPhysical and Theoretical ChemistryBODIPYEuropean Journal of Organic Chemistry
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Synthesis and radiosynthesis of N5-[18F]fluoroethyl-Pirenzepine and its metabolite N5-[18F]fluoroethyl-LS 75

2009

The well established M1 selective muscarinergic antagonist Pirenzepine 11-[2-(4-methyl-piperazin-1-yl)-acetyl]-5,11-dihydro-benzo[e]pyrido[3,2-b][1,4]diazepin-6-one (1) exhibits an unusual behaviour in vivo, which cannot be explained with M1 antagonism exclusively. One of the aspects discussed is a specific interaction with poly ADP-ribose polymerase (PARP-1). 1 undergoes metabolism to form LS 75 5,11-dihydro-benzo[e]pyrido[3,2-b][1,4]diazepin-6-one (2). In order to study deviations in Pirenzepine efficacy from pure M1 binding in vivo using PET, appropriate positron emitter labelled analogues of 1 and 2 were synthesised. Non-radioactive reference compounds 3 and 4 were tested for PARP-1 inh…

Chemistrymedicine.drug_classStereochemistryMetaboliteOrganic ChemistryRadiosynthesisCarboxamideBiochemistryPirenzepineChemical synthesisAnalytical Chemistrychemistry.chemical_compoundDrug DiscoveryLipophilicitymedicineLactamRadiology Nuclear Medicine and imagingSpectroscopyFluoroethylmedicine.drugJournal of Labelled Compounds and Radiopharmaceuticals
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P.21.2 New insights into eosinophilic fasciitis

2013

Eosinophilic fasciitis (EF), first described by Shulman in 1974, is a rare disease characterized by fibrosis and inflammatory infiltration of the muscle fascia as well as scleroderma-like skin indurations and blood eosinophilia. In contrast to other inflammatory myopathies, patients generally show less muscle weakness and myalgia, and a frequent increase in body weight. Thus, we hypothesize a unique immune mechanism underlying Shulman syndrome. The immunohistochemical expression pattern of leucocytes and a comprehensive panel of cytokine and chemokine expression on RNA level of muscle specimen from EF patients were compared to healthy control muscle. In patients with biopsy-proven EF the im…

ChemokinePathologymedicine.medical_specialtybiologymedicine.medical_treatmentT helper cellmedicine.diseaseEosinophilic fasciitisImmune systemmedicine.anatomical_structureCytokineNeurologyPediatrics Perinatology and Child HealthMHC class IImmunologybiology.proteinmedicineMacrophageNeurology (clinical)Genetics (clinical)CD8Neuromuscular Disorders
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Solution-, solid-phase, and fluorous synthesis of beta,beta-difluorinated cyclic quaternary alpha-amino acid derivatives: a comparative study.

2008

The diastereoselective synthesis of cyclic beta,beta-difluorinated alpha-amino acid derivatives bearing a quaternary stereocenter is described. The process relies on the chemo- and diastereoselective addition of allylic organometallic reagents to fluorinated alpha-imino esters and a subsequent ring-closing metathesis reaction (RCM). Complete selectivity in the nucleophilic addition was achieved with (R)-phenylglycinol methyl ether as a chiral auxiliary. The resulting amino acids were introduced into peptide chains, which could facilitate the preparation of potentially bioactive dipeptide derivatives. In addition, the solution synthesis of these cyclic fluorinated alpha-amino acids was succe…

Chiral auxiliaryAllylic rearrangementNucleophilic additionDipeptideMolecular StructureChemistryOrganic ChemistryFluorine CompoundsAmino Acids CyclicEtherEstersStereoisomerismGeneral ChemistryCatalysisStereocenterSolutionschemistry.chemical_compoundSolid-phase synthesisSalt metathesis reactionOrganic chemistryIminesProtonsAminationChemistry (Weinheim an der Bergstrasse, Germany)
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Iron-Catalyzed C(sp2)–C(sp3) Cross-Coupling of Aryl Chlorobenzoates with Alkyl Grignard Reagents

2020

Aryl benzoates are compounds of high importance in organic synthesis. Herein, we report the iron-catalyzed C(sp2)&ndash

Chlorobenzoatesaryl estersPharmaceutical ScienceMedicinal chemistryArticleCatalysisAnalytical ChemistryCatalysislcsh:QD241-441chemistry.chemical_compoundironlcsh:Organic chemistryDrug Discoverycross-couplingPhysical and Theoretical ChemistryAlkylchemistry.chemical_classificationNucleophilic additionMolecular StructureArylOrganic ChemistryBenzoatesChlorobenzoateschemistryChemistry (miscellaneous)Fe-catalysisFunctional groupKumada cross-couplingMolecular MedicineOrganic synthesisC–O activationIron CompoundsMolecules
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