Search results for "building-block"

showing 8 items of 8 documents

On the synthesis of functionalized porphyrins and porphyrin conjugates via β-aminoporphyrins

2016

International audience; The synthesis of functionalized porphyrins and their conjugates from meso-tetraarylporphyrins through the acylation and the oxidation of beta-aminoporphyrins was investigated. 2,3-Dioxochlorins were prepared by the oxidation of a variety of beta-aminoporphyrins and subsequently used in a condensation reaction with functionalized aromatic aldehydes and ammonium acetate to form beta-functionalized porphyrins bearing a fused imidazole ring. Under optimized experimental conditions both reactions tolerate various functional groups and afford the products in an appropriate overall yield. The mildness and usefulness of this methodology are illustrated by several examples in…

coordination010402 general chemistryRing (chemistry)01 natural sciences[ CHIM ] Chemical SciencesCatalysisphotoinduced electron-transferAcylationchemistry.chemical_compoundMaterials Chemistrypolycyclic compoundsImidazoleOrganic chemistry[CHIM]Chemical Sciencesalpha-dionesbuilding-blockspyrrolic position010405 organic chemistrysensitized solar-cellsbodipy dyesGeneral Chemistryefficient peripheral functionalizationCondensation reactionCombinatorial chemistryPorphyrin0104 chemical scienceswater-solubilizationchemistryYield (chemistry)systemsAmmonium acetateConjugate
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Diastereoselective synthesis of 6-functionalized 4-aryl-1,3-oxazinan-2-ones and their application in the synthesis of 3-aryl-1,3-aminoalcohols and 6-…

2010

Abstract Halocyclocarbamation of benzyl N -(1-phenyl-3-butenyl)carbamates afforded 6-functionalized 4-aryl-1,3-oxazinan-2-ones with moderate to excellent diastereoselectivity depending on the N -substituent. Importantly, in contrast to reported cyclocarbamations of homoallylic carbamates, which are generally trans -diastereoselective, cyclization of N -unsubstituted Cbz-protected homoallylamines led to cis -1,3-oxazinan-2-ones, predominantly. The use of N -benzylated and in situ prepared N -silylated derivatives resulted however in trans -selectivity. Transition states are proposed to explain the stereochemical influence of the N -substituent on the cyclocarbamations. The functionalized 1,3…

3-AminoalcoholsStereochemistry3-ASYMMETRIC INDUCTION1SubstituentBiochemistrychemistry.chemical_compound4-dionesCHIRAL BUILDING-BLOCKDrug DiscoveryHEIMIA-SALICIFOLIAArylOrganic ChemistryCONCISE SYNTHESISHOMOALLYLIC AMINESTransition stateALPHA-AMINO-ACIDSChemistrySTEREOSELECTIVE-SYNTHESISCyclocarbamationSTREPTOMYCES-CLAVULIGERUSchemistryASYMMETRIC TOTAL-SYNTHESISINTRAMOLECULAR AMIDOALKYLATION3-Oxazinan-2-onesPiperidine-2
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Efficient microwave-assisted synthesis of glycerol monodecanoate

2017

International audience; Solvent-free microwave-assisted synthesis was carried out to prepare 2,3-dihydroxypropyl decanoate, by esterification of decanoic acid in the presence of two distinct glycerol derivatives, glycidol, and glycerol carbonate, respectively. The process described is based on microwaves heating source with electrical power in the range of 200–400 W, involving stoichiometric proportions of decanoic acid and glycerol derivatives, and using catalytic amounts of TBAI used as organocatalyst. Conversion and selectivity rates of esterification reactions were monitored by 1H and 13C{1H} NMR spectroscopy. The predominantly formed ester, 2,3-dihydroxypropyl decanoate was fully chara…

Green chemistryBio-based building-blocksGlycerol derivatives02 engineering and technology010402 general chemistry01 natural sciences[ CHIM ] Chemical SciencesIndustrial and Manufacturing EngineeringCatalysischemistry.chemical_compoundGlycerolOrganic chemistry[CHIM]Chemical Sciences1-MonoacylglycerolComputingMilieux_MISCELLANEOUSGlycidolGeneral ChemistryDecanoic acidNuclear magnetic resonance spectroscopy021001 nanoscience & nanotechnology0104 chemical sciencesMicrowave-assisted organic chemistrychemistryGreen chemistry13. Climate action0210 nano-technologySelectivityStoichiometryFood ScienceBiotechnology
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Undecylenic acid: A tunable bio-based synthon for materials applications

2016

International audience; An undecylenic acid-based monoglyceride prepared from glycidol and undecylenic acid is used as suitable and tunable synthon for polymerization applications. Epoxidation and acrylation reactions lead to photopolymerizable monomers while transesterification with dimethyl carbonate, metathesis and aminolysis reactions provide access to polyhydroxyurethane-based materials. The successive intermediates were synthesized according to a green chemistry approach implicating solvent-less and catalyzed reactions, and were at each step fully characterized by infrared, 1H and 13C{1H} NMR spectroscopy, elemental analysis and mass spectrometry. Analyses of the resulting polymer mat…

Green chemistryThermogravimetric analysisRenewable resourcesMaterials sciencePolymers and PlasticsOrganic carbonatepolyhydroxyurethanespolyurethanesGeneral Physics and Astronomy02 engineering and technologycyclic carbonates010402 general chemistry01 natural sciences[ CHIM ] Chemical Scienceschemistry.chemical_compoundPolyhydroxyurethanes (PHUs)Aminolysisrenewable building-blockPolymer chemistryMaterials ChemistrymedicineOrganic chemistry[CHIM]Chemical Sciencessolvent-free conditionscastor-oilglycerol carbonatePhotopolymerizationOrganic ChemistrySynthonGlycidolTransesterification021001 nanoscience & nanotechnologyFatty acid0104 chemical scienceschemistryPolymerizationGlycidolpolycarbonatespolymerizationUndecylenic acidderivatives0210 nano-technologymedicine.drug
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Ring splitting of azetidin-2-ones via radical anions

2012

The radical anions of azetidin-2-ones, generated by UV-irradiation in the presence of triethylamine, undergo ring-splitting via N-C4 or C3-C4 bond breaking, leading to open-chain amides. This reactivity diverges from that found for the neutral excited states, which is characterised by alpha-cleavage. The preference for beta-cleavage is supported by DFT theoretical calculations on the energy barriers associated with the involved transition states. Thus, injection of one electron into the azetidin-2-one moiety constitutes a complementary activation strategy which may be exploited to produce new chemistry.

AnionsAZETIDINESFree RadicalsUltraviolet RaysElectronVINYL ETHERSRing (chemistry)PhotochemistryBiochemistryPolarizable continuum modelchemistry.chemical_compoundN-(ARYLIDENE(OR ALKYLIDENE)AMINO)-2-AZETIDINONESQUIMICA ORGANICAMoietyReactivity (chemistry)BETA-LACTAM RINGPhysical and Theoretical ChemistryTriethylamineDNA PHOTOLYASEMolecular StructureSTEREOCONTROLLED SYNTHESISOrganic ChemistryTransition stateSTEREOSELECTIVE-SYNTHESISchemistryPOLARIZABLE CONTINUUM MODELExcited stateQuantum TheoryPHOTOCHEMICAL-REACTIONSBUILDING-BLOCKS
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Weighting non-covalent forces in the molecular recognition of C60. Relevance of concave–convex complementarity

2008

The relative contributions of several weak intermolecular forces to the overall stability of the complexes formed between structurally related receptors and [60]fullerene are compared, revealing a discernible contribution from concave–convex complementarity. Viruela Martin, Pedro Manuel, Pedro.M.Viruela@uv.es ; Viruela Martin, Rafael, Rafael.Viruela@uv.es ; Orti Guillen, Enrique, Enrique.Orti@uv.es

FULLERENESUNESCO::QUÍMICANon covalentBUILDING-BLOCK12-TETRACYANO-9:QUÍMICA [UNESCO]CatalysisMolecular recognitionCHEMISTRYSYSTEMSMaterials ChemistryUNESCO::QUÍMICA::Química orgánicaCARBON NANORINGSChemistryCARBON NANORINGS; BUILDING-BLOCK; FULLERENES; 11111212-TETRACYANO-910-ANTHRAQUINODIMETHANE; COMPLEXATION; DERIVATIVES; RECEPTORS; CHEMISTRY; SYSTEMSCOMPLEXATIONDERIVATIVESIntermolecular force:QUÍMICA::Química orgánica [UNESCO]Metals and AlloysRegular polygonMolecular recognition ; Concave-convex ; Stability ; C60 ; Intermolecular forcesGeneral ChemistrySettore CHIM/06 - Chimica Organica11Intermolecular forcesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsWeighting12Concave-convexbody regionsRECEPTORSC60CrystallographyChemical physicsComplementarity (molecular biology)10-ANTHRAQUINODIMETHANECeramics and CompositesMolecular recognitionStability
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Direct catalytic cross-coupling of alkenyllithium compounds

2015

A catalytic method for the direct cross-coupling of alkenyllithium reagents with aryl and alkenyl halides is described. The use of a catalyst comprising Pd-2(dba)(3)/XPhos allows for the stereoselective preparation of a wide variety of substituted alkenes in high yields under mild conditions. In addition (1-ethoxyvinyl) lithium can be efficiently converted into substituted vinyl ethers which, after hydrolysis, give readily access to the corresponding methyl ketones in a one pot procedure.

Química organometàl·licaHalidechemistry.chemical_element010402 general chemistry01 natural sciencesORGANOLITHIUM COMPOUNDSCatalysischemistry.chemical_compoundNOBEL-PRIZECatàlisiXPhosOrganic chemistryREAGENTSARYL CHLORIDES010405 organic chemistryChemistryPALLADIUMArylGeneral ChemistryCombinatorial chemistry0104 chemical sciencesCARBON-CARBONORGANIC HALIDESReagentStereoselectivityLithiumSMALL-MOLECULE SYNTHESISPalladiumORTHO-METALATIONBUILDING-BLOCKS
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A Very Low Band Gap Diketopyrrolopyrrole-Porphyrin Conjugated Polymer

2017

International audience; A porphyrin-diketopyrrolopyrrole-containing polymer (poly(porphyrin-diketopyrrolopyrrole) (PPDPP)) shows impressive molar absorption coefficients from lambda=300 to 1000 nm. The photophysical and structural properties of PPDPP have been studied. With PPDPP as the electron donor and [ 6,6]phenyl C-71 butyric acid methyl ester (PC71BM) as the electron acceptor, the bulk heterojunction polymer solar cell showed overall power conversion efficiencies of 4.18 and 6.44% for as-cast and two-step annealing processed PPDPP: PC71BM (1: 2) active layers, respectively. These results are quite impressive for porphyrin-containing polymers, especially when directly included in the p…

Materials scienceBand gapbuilding-blockporphyrinoidsElectron donorthin-film transistors02 engineering and technologyConjugated system010402 general chemistryPhotochemistry[ CHIM ] Chemical Sciences01 natural sciencesPolymer solar cellheterojunction solar-cellschemistry.chemical_compound[CHIM]Chemical Sciencessmall-moleculepolymerschemistry.chemical_classificationsemiconducting polymerscharge transferGeneral ChemistryPolymerChromophoreElectron acceptorside-chains021001 nanoscience & nanotechnologyPorphyrinphotovoltaic properties0104 chemical sciencesphotodynamic therapychemistryorganic photovoltaics0210 nano-technologyabsorptionperformanceconjugationChemPlusChem
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