Search results for "combinatorial"

showing 10 items of 1208 documents

Synthesis of new fluorescent amino acids with a triazolopyridine core: diacid sensors

2018

A new family of amino acid containing pyridine–triazolopyridine cores has been prepared by means of a copper catalysed reaction. These compounds exhibit an intense emission that has been employed to sense the distance between two carboxylic acids in a linear molecule, from oxalic to glutaric acids.

chemistry.chemical_classification010405 organic chemistryChemistrychemistry.chemical_elementGeneral Chemistry010402 general chemistry01 natural sciencesCopperCombinatorial chemistryFluorescenceCatalysis0104 chemical sciencesAmino acidCore (optical fiber)Materials ChemistryTriazolopyridine
researchProduct

Strategies for Exploring Functions from Dynamic Combinatorial Libraries

2020

chemistry.chemical_classification010405 organic chemistryComputer scienceMechanical EngineeringSupramolecular chemistryEnergy Engineering and Power TechnologyNanotechnologyManagement Science and Operations Research010402 general chemistry01 natural sciencesKinetic control0104 chemical scienceschemistryDynamic combinatorial chemistryNon-covalent interactionsChemSystemsChem
researchProduct

2018

A visible light-promoted protocol for the redox-neutral coupling of N-hydroxyphthalimide esters with different N-heterocyclic compounds is described. The reaction proceeds through an alkyl radical intermediate generated by reductive decarboxylation of N-hydroxyphthalimide esters. In contrast to the original Minisci protocol, polyalkylation can largely be avoided. Mechanistic investigations revealed a radical chain mechanism which in some cases can proceed even if no photocatalyst is added. This valuable and functional group-tolerant reaction produces substituted heterocycles in moderate to excellent yield. The use of inexpensive starting materials and LEDs as the light source are key featur…

chemistry.chemical_classification010405 organic chemistryDecarboxylationOrganic ChemistryPharmaceutical Science010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesAnalytical ChemistryCatalysischemistryChemistry (miscellaneous)Yield (chemistry)Drug DiscoveryPhotocatalysisMolecular MedicineMoleculePhysical and Theoretical ChemistryAlkylMinisci reactionVisible spectrumMolecules
researchProduct

Engineering faster transglycosidases and their acceptor specificity

2019

Transglycosidases are enzymes that have the potential to catalyze the synthesis of a wide range of high-value compounds starting from biomass-derived feedstocks. Improving their activity and broadening the substrate range are important goals to enable the widespread application of this family of biocatalysts. In this work, we engineered 20 mutants of the rice transglycosidase Os9BGlu31 and evaluated their catalysis in 462 reactions over 18 different substrates. This allowed us to identify mutants that expanded their substrate range and showed high activity, including W243L and W243N. We also developed double mutants that show very high activity on certain substrates and exceptional specific…

chemistry.chemical_classification010405 organic chemistryExternal validationSubstrate (chemistry)010402 general chemistry01 natural sciencesPollutionAcceptorCombinatorial chemistry0104 chemical sciencesCatalysisEnzymechemistryCheminformaticsEnvironmental ChemistryHigh activityGreen Chemistry
researchProduct

Highly Functionalized Brønsted Acidic/Lewis Basic Hybrid Ferrocene Ligands: Synthesis and Coordination Chemistry

2019

International audience; A general challenging issue in the synthesis of hemilabile ferrocene ligands is the access to highly functionalized ferrocene starting materials. These can bear donor/acceptor atoms, additional functional and structuring spectator substituents, but the preparation of such species poses general synthetic difficulties. We report herein alternative synthetic routes to hybrid ferrocene donors such as tert-butylated phosphanylcarboxylic acids and their corresponding aldehydes. These hybrid ambiphilic species that combine Brønsted-acidic and Lewis-basic functional moieties in their structure were characterized by multinuclear NMR and single-crystal X-ray diffraction analys…

chemistry.chemical_classification010405 organic chemistryHydrogen bondSolid-state010402 general chemistry01 natural sciencesCombinatorial chemistryAcceptor0104 chemical sciencesCoordination complexInorganic Chemistrychemistry.chemical_compoundFerrocenechemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryBrønsted–Lowry acid–base theoryMutual influence
researchProduct

Organic chelate-free and azido-rich metal clusters and coordination polymers from the use of Me3SiN3: a new synthetic route to complexes with beautif…

2019

In this Feature Article, we highlight the feasibility of a new, recently developed approach towards the synthesis of high-spin molecules and single-molecule magnets (SMMs). The key to the preparation of such molecular compounds is the organic azide precursor Me3SiN3, which fosters the formation of 3d-metal azido clusters and coordination polymers without requiring the assistance of any organic chelating/bridging group. All the isolated compounds contain metallic cores which are surrounded by end-on bridging N3− groups. Consequently, the reported molecular materials exhibit ferromagnetic exchange interactions between the spin carriers, resulting in the stabilization of the maximum possible s…

chemistry.chemical_classification010405 organic chemistryMetals and AlloysGeneral ChemistryPolymer010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsCoordination complexMetalchemistry.chemical_compoundMagnetic anisotropyFerromagnetismchemistryvisual_artReagentMaterials ChemistryCeramics and Compositesvisual_art.visual_art_mediumMoleculeAzideChemical Communications
researchProduct

Synthesis of l -[4-11 C]Asparagine by Ring-Opening Nucleophilic 11 C-Cyanation Reaction of a Chiral Cyclic Sulfamidate Precursor

2018

The development of a convenient and rapid method to synthesize radiolabeled, enantiomerically pure amino acids (AAs) as potential positron emission tomography (PET) imaging agents for mapping various biochemical transformations in living organisms remains a challenge. This is especially true for the synthesis of carbon-11-labeled AAs given the short half-life of carbon-11 (11 C, t1/2 =20.4 min). A facile synthetic pathway to prepare enantiomerically pure 11 C-labeled l-asparagine was developed using a partially protected serine as a starting material with a four-step transformation providing a chiral five-membered cyclic sulfamidate as the radiolabeling precursor. Its structure and absolute…

chemistry.chemical_classification010405 organic chemistryOrganic ChemistryAbsolute configurationStereoisomerismGeneral ChemistryCyanation010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesAmino acidHydrolysisNucleophilechemistryYield (chemistry)AsparagineChemistry - A European Journal
researchProduct

P-Chirogenic Triazole-Based Phosphine: Synthesis, Coordination Chemistry, and Asymmetric Catalysis

2020

chemistry.chemical_classification010405 organic chemistryOrganic ChemistryEnantioselective synthesisTriazole010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesCoordination complexchemistry.chemical_compoundchemistryTransition metalPhysical and Theoretical ChemistryPhosphineEuropean Journal of Organic Chemistry
researchProduct

Cross-Linked Polyamine from Imidazolium-Based Materials: A Simple Route to Useful Catalytic Materials

2018

chemistry.chemical_classification010405 organic chemistryOrganic ChemistryPolymer010402 general chemistryHeterogeneous catalysis01 natural sciencesCombinatorial chemistry0104 chemical sciencesCatalysischemistry.chemical_compoundchemistrySimple (abstract algebra)Ionic liquidPhysical and Theoretical ChemistryPolyamineEuropean Journal of Organic Chemistry
researchProduct

A novel synthetic approach to pyran-2,4-dione scaffold production: Microwave-assisted dimerization, cyclization, and expeditious regioselective conve…

2020

Abstract Here, we report a novel, green, simple, low-cost, and rapid methodology for the high-yield production of pyran-2,4-dione scaffolds under microwave irradiation. Regio- and stereoselective conversions of β-diketone systems into β-enaminones were achieved using 18 primary amines and four amino acid esters. Microwave-assisted further cyclization of 3-(β-substitutedvinyl)-6-phenyl-pyran-2,4-dione into 3-benzoyl-4,7-diphenyl-2H,5H-pyrano[4,3-b]pyran-2,5-dione via reaction with ethyl benzoyl acetate.

chemistry.chemical_classification010405 organic chemistryOrganic ChemistryRegioselectivity010402 general chemistry01 natural sciencesBiochemistryMicrowave assistedCombinatorial chemistry0104 chemical sciencesAmino acidchemistry.chemical_compoundchemistryPyranDrug DiscoveryMicrowave irradiationStereoselectivityTetrahedron Letters
researchProduct