Search results for "Full Research Paper"

showing 10 items of 80 documents

Stereoselective cathodic synthesis of 8-substituted (1R,3R,4S)-menthylamines.

2015

The electrochemical generation of menthylamines from the corresponding menthone oximes equipped with an additional substituent in position 8 is described. Due to 1,3-diaxial interactions a pronounced diastereoselectivity for the menthylamines is found.

Organic ChemistrySubstituentoximesElectrochemistryElectrosynthesisCombinatorial chemistryMenthonementhylaminesFull Research PaperCathodic protectionlcsh:QD241-441chemistry.chemical_compoundChemistryelectrosynthesislcsh:Organic chemistrychemistryOrganic chemistrylcsh:QStereoselectivitylcsh:Sciencecathodic reductionchiral aminesBeilstein journal of organic chemistry
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Thermodynamic and electrochemical study of tailor-made crown ethers for redox-switchable (pseudo)rotaxanes

2020

Crown ethers are common building blocks in supramolecular chemistry and are frequently applied as cation sensors or as subunits in synthetic molecular machines. Developing switchable and specifically designed crown ethers enables the implementation of function into molecular assemblies. Seven tailor-made redox-active crown ethers incorporating tetrathiafulvalene (TTF) or naphthalene diimide (NDI) as redox-switchable building blocks are described with regard to their potential to form redox-switchable rotaxanes. A combination of isothermal titration calorimetry and voltammetric techniques reveals correlations between the binding energies and redox-switching properties of the corresponding ps…

RotaxaneSupramolecular chemistryElectrochemistryRedoxFull Research Papersupramolecular chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryComputational chemistryredox chemistrysupramolekulaarinen kemialcsh:ScienceCrown etherchemistry.chemical_classificationOrganic ChemistryIsothermal titration calorimetry540Molecular machineisothermal titration calorimetryChemistryrotaxaneschemistrycrown etherlcsh:Q500 Naturwissenschaften und Mathematik::540 Chemie::540 Chemie und zugeordnete WissenschaftenTetrathiafulvaleneBeilstein Journal of Organic Chemistry
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Stereoselective synthesis and transformation of pinane-based 2-amino-1,3-diols

2021

A library of pinane-based 2-amino-1,3-diols was synthesised in a stereoselective manner. Isopinocarveol prepared from (−)-α-pinene was converted into condensed oxazolidin-2-one in two steps by carbamate formation followed by a stereoselective aminohydroxylation process. The relative stereochemistry of the pinane-fused oxazolidin-2-one was determined by 2D NMR and X-ray spectroscopic techniques. The regioisomeric spiro-oxazolidin-2-one was prepared in a similar way starting from the commercially available (1R)-(−)-myrtenol (10). The reduction or alkaline hydrolysis of the oxazolidines, followed by reductive alkylation resulted in primary and secondary 2-amino-1,3-diols, which underwent a reg…

ScienceAlkaline hydrolysis (body disposal)Alkylation2-amino-12-diol010402 general chemistryRing (chemistry)01 natural sciencesFull Research PaperBenzaldehydechemistry.chemical_compoundQD241-441monoterpeenitOrganic chemistryorgaaniset yhdisteetkemiallinen synteesistereoselective010405 organic chemistryQOrganic ChemistryRegioselectivityTautomer0104 chemical sciencesChemistrytautomerismchemistryoxazolidin-2-oneStereoselectivityTwo-dimensional nuclear magnetic resonance spectroscopytautomeriamonoterpeneBeilstein Journal of Organic Chemistry
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Self-assembly of metallosupramolecular rhombi from chiral concave 9,9'-spirobifluorene-derived bis(pyridine) ligands.

2014

Two new 9,9’-spirobifluorene-based bis(4-pyridines) were synthesised in enantiopure and one also in racemic form. These ligands act as concave templates and form metallosupramolecular [(dppp)2M2L2] rhombi with cis-protected [(dppp)Pd]2+ and [(dppp)Pt]2+ ions. The self-assembly process of the racemic ligand preferably occurs in a narcissistic self-recognising manner. Hence, a mixture of all three possible stereoisomers [(dppp)2M2{(R)-L}2](OTf)4, [(dppp)2M2{(S)-L}2](OTf)4, and [(dppp)2M2{(R)-L}{(S)-L}](OTf)4 was obtained in an approximate 1.5:1.5:1 ratio which corresponds to an amplification of the homochiral assemblies by a factor of approximately three as evidenced by NMR spectroscopy and m…

Stereochemistryconcave templatesSupramolecular chemistrymetal complexesFull Research Paperself-sortingsupramolecular chemistrylcsh:QD241-441lcsh:Organic chemistrysupramolekulaarinen kemialcsh:Scienceta1169LigandChemistryOrganic ChemistryNuclear magnetic resonance spectroscopyself-assemblyPyridine ligandCrystallographyChemistrySelf sortingEnantiopure drug99’-spirobifluorenelcsh:QSelf-assembly9’-spirobifluoreneSingle crystalBeilstein journal of organic chemistry
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Binding abilities of a chiral calix[4]resorcinarene: a polarimetric investigation on a complex case of study

2017

Polarimetry was used to investigate the binding abilities of a chiral calix[4]resorcinarene derivative, bearing L-proline subunits, towards a set of suitably selected organic guests. The simultaneous formation of 1:1 and 2:1 host–guest inclusion complexes was observed in several cases, depending on both the charge status of the host and the structure of the guest. Thus, the use of the polarimetric method was thoroughly revisited, in order to keep into account the occurrence of multiple equilibria. Our data indicate that the stability of the host–guest complexes is affected by an interplay between Coulomb interactions, π–π interactions, desolvation effects and entropy-unfavorable conformatio…

Supramolecular chemistryPolarimetryhost–guest complexes010402 general chemistry01 natural scienceshost-guest complexesFull Research Papersupramolecular chemistrylcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryComputational chemistryp-nitroanilinesDesolvationlcsh:Sciencepolarimetrycalix[4]resorcinarene010405 organic chemistryChemistryOrganic ChemistryHost-guest complexeSettore CHIM/06 - Chimica OrganicaResorcinarene0104 chemical sciencesChemistrylcsh:QP-nitroanilineDerivative (chemistry)Beilstein Journal of Organic Chemistry
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Synthesis and biological evaluation of a novel MUC1 glycopeptide conjugate vaccine candidate comprising a 4’-deoxy-4’-fluoro-Thomsen–Friedenreich epi…

2015

The development of selective anticancer vaccines that provide enhanced protection against tumor recurrence and metastasis has been the subject of intense research in the scientific community. The tumor-associated glycoprotein MUC1 represents a well-established target for cancer immunotherapy and has been used for the construction of various synthetic vaccine candidates. However, many of these vaccine prototypes suffer from an inherent low immunogenicity and are susceptible to rapid in vivo degradation. To overcome these drawbacks, novel fluorinated MUC1 glycopeptide-BSA/TTox conjugate vaccines have been prepared. Immunization of mice with the 4’F-TF-MUC1-TTox conjugate resulted in strong im…

Synthetic vaccinemedicine.medical_treatmentMUC1Full Research PaperEpitopelcsh:QD241-441Immune systemCancer immunotherapylcsh:Organic chemistryConjugate vaccinemedicineskin and connective tissue diseaseslcsh:Scienceneoplasmsfluorinated carbohydratescancer immunotherapyChemistryImmunogenicityOrganic ChemistryTACAdigestive system diseasesglycoconjugatesChemistryImmunizationImmunologyCancer researchlcsh:QConjugateBeilstein Journal of Organic Chemistry
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Manipulation of nanoparticles of different shapes inside a scanning electron microscope

2014

In this work polyhedron-like gold and sphere-like silver nanoparticles (NPs) were manipulated on an oxidized Si substrate to study the dependence of the static friction and the contact area on the particle geometry. Measurements were performed inside a scanning electron microscope (SEM) that was equipped with a high-precision XYZ-nanomanipulator. To register the occurring forces a quartz tuning fork (QTF) with a glued sharp probe was used. Contact areas and static friction forces were calculated by using different models and compared with the experimentally measured force. The effect of NP morphology on the nanoscale friction is discussed.

Work (thermodynamics)Materials scienceScanning electron microscopeGeneral Physics and AstronomyNanoparticleNanotechnologyscanning electron microscopy (sem)lcsh:Chemical technologylcsh:TechnologyFull Research PaperSilver nanoparticlecontact mechanicsNanotechnologynanomanipulationlcsh:TP1-1185General Materials ScienceElectrical and Electronic EngineeringComposite materiallcsh:ScienceNanoscopic scalelcsh:Tnanotribologylcsh:QC1-999NanoscienceContact mechanicsNanotribologynanoparticleslcsh:QContact arealcsh:PhysicsBeilstein Journal of Nanotechnology
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Synthesis of highly functionalized β-aminocyclopentanecarboxylate stereoisomers by reductive ring opening reaction of isoxazolines

2012

A rapid and simple procedure was devised for the synthesis of multifunctionalized cyclic β-amino esters and γ-amino alcohols via the 1,3-dipolar cycloaddition of nitrile oxides to β-aminocyclopentenecarboxylates. The opening of the isoxazoline reductive ring to the corresponding highly functionalized 2-aminocyclopentanecarboxylates occurred stereoselectively with good yields.

amino acidsNitrileOrganic ChemistryreductionisoxazolinesRing (chemistry)CycloadditionFull Research Paperlcsh:QD241-441chemistry.chemical_compoundChemistrychemistrylcsh:Organic chemistryOrganic chemistryfunctionalizationlcsh:Qlcsh:Scienceta116cycloadditionBeilstein Journal of Organic Chemistry
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Synthesis of fluorescent (benzyloxycarbonylamino)(aryl)methylphosphonates

2014

The synthesis of a library of structurally variable aromatic esters of (benzyloxycarbonylamino)(aryl)methylphosphonic acids is described by means of the Oleksyszyn reaction. The library was enlarged by the application of a Suzuki–Miayra approach and by preparation of mixed esters.

aminophosphonatesArylOrganic ChemistryorganophosphorusFluorescenceFull Research Paperlcsh:QD241-441ChemistryZ-aminophosphonate esterschemistry.chemical_compoundlcsh:Organic chemistrychemistryOrganic chemistrylcsh:Qlcsh:ScienceOleksyszyn reactionBeilstein Journal of Organic Chemistry
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Tanzawaic acids I-L: Four new polyketides from Penicillium sp. IBWF104-06.

2014

Four new polyketides have been identified in culture filtrates of the fungal strain Penicillium sp. IBWF104-06 isolated from a soil sample. They are structurally based on the same trans-decalinpentanoic acid skeleton as tanzawaic acids A–H. One of the new compounds was found to inhibit the conidial germination in the rice blast fungus Magnaporthe oryzae at concentrations of 25 μg/mL.

biologyChemistrynatural productsOrganic Chemistrystructure elucidationfood and beveragesFungusbiology.organism_classificationFull Research PaperarohynapeneMicrobiologylcsh:QD241-441Magnaporthe oryzaeChemistrylcsh:Organic chemistryGerminationPenicilliumtanzawaic acidFungal strainlcsh:Qlcsh:SciencepolyketidesBeilstein journal of organic chemistry
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