Search results for "Synthesis"

showing 10 items of 2844 documents

Auxiliary-controlled stereoselective enolate protonation: Enantioselective synthesis of cis and trans annulated decahydroquinoline alkaloids

1998

Abstract The diastereoselective synthesis of the octahydroquinoline enone precursor of pumiliotoxin C is achieved via tandem Mannich-Michael reaction on N-galactosyl imines. Conjugate cuprate addition to the bicyclic enone stereoselectively forms the trans annulated 4a- epi -pumiliotoxin C skeleton in the presence of the carbohydrate auxiliary, and the cis annulated pumiliotoxin C skeleton in its absence.

Bicyclic moleculeStereochemistryOrganic ChemistryEnantioselective synthesisProtonationBiochemistrychemistry.chemical_compoundPumiliotoxin CchemistryDrug DiscoveryStereoselectivityEnoneCis–trans isomerismConjugateTetrahedron Letters
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Preparation of dopaminergic N-alkyl-benzyltetrahydroisoquinolines using a 'one-pot' procedure in acid medium.

2000

The preparation of N-methyl-BTHIQ (4) from N-phenylethyl-phenacetamide (1) by cyclization, reduction and N-alkylation in acid medium has been achieved in good yield in a 'one-pot' procedure. Acylation of imine (2) intermediate afforded the Z and E stereoselectivity in the enamide formation. 6-Hydroxy-BTHIQ (7) shows selectivity for D2 dopamine receptors, while its N-methylated homologue (8) displays higher affinities for both D1 and D2 receptor types, with an unexpected increase in D1 dopamine receptor affinity.

Bicyclic moleculeStereochemistryReceptors Dopamine D2Receptors Dopamine D1Spectrum AnalysisOrganic ChemistryClinical BiochemistryDopaminergicImineDopamine AgentsPharmaceutical ScienceIsoquinolinesBiochemistryChemical synthesisAcylationchemistry.chemical_compoundchemistryDopamine receptor D2Drug DiscoveryMolecular MedicineStereoselectivitySelectivityMolecular Biology
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Two-carbon bridge substituted cocaines: enantioselective synthesis, attribution of the absolute configuration and biological activity of novel 6- and…

1999

In an effort to learn more about the general structure-activity relationships of cocaine with the aim to elucidate those structural features that might confer antagonistic properties to such analogues, we describe herein our synthetic efforts to prepare two-carbon bridge functionalized (methoxylated and hydroxylated) analogues. Our approach makes use of a modification of the classical Willstatter synthesis of cocaine: Mannich type cyclization of acetonedicarboxylic acid monomethyl ester with methylamine hydrochloride and 2-methoxysuccindialdehyde in a citrate buffer solution afforded the 6- and 7-substituted 2-carbomethoxy-3-tropinones 3a,b and 4a,b in approximate yields of 64%. Reduction o…

Bicyclic moleculeSwineStereochemistryAcetonedicarboxylic acidAbsolute configurationEnantioselective synthesisPharmaceutical ScienceStereoisomerismStereoisomerismSodium amalgamChemical synthesisRatsStructure-Activity Relationshipchemistry.chemical_compoundCocainechemistryDrug DiscoveryAnimalsEnantiomerIl Farmaco
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Mass measurements beyond the major r-process waiting point $^{80}$Zn

2008

High-precision mass measurements on neutron-rich zinc isotopes 71m,72-81Zn have been performed with the Penning trap mass spectrometer ISOLTRAP. For the first time the mass of 81Zn has been experimentally determined. This makes 80Zn the first of the few major waiting points along the path of the astrophysical rapid neutron capture process where neutron separation energy and neutron capture Q-value are determined experimentally. As a consequence, the astrophysical conditions required for this waiting point and its associated abundance signatures to occur in r-process models can now be mapped precisely. The measurements also confirm the robustness of the N = 50 shell closure for Z = 30 farthe…

Binding energies and massessupernovaeNucleosynthesis in novaeand other explosive environmentsFOS: Physical sciencesNuclear Physics - Experiment59<=A<=89[PHYS.NEXP]Physics [physics]/Nuclear Experiment [nucl-ex]Nuclear Experiment (nucl-ex)Nuclear ExperimentNuclear Experiment
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Photoluminescent and Slow Magnetic Relaxation Studies on Lanthanide(III)-2,5-pyrazinedicarboxylate Frameworks

2017

In the series described in this work, the hydrothermal synthesis led to oxidation of the 5-methyl-pyrazinecarboxylate anion to the 2,5-pyrazinedicarboxylate dianion (2,5-pzdc) allowing the preparation of three-dimensional (3D) lanthanide(III) organic frameworks of formula {[Ln2(2,5-pzdc)3(H2O)4]·6H2O}n [Ln = Ce (1), Pr (2), Nd (3), and Eu (4)] and {[Er2(2,5-pzdc)3(H2O)4]·5H2O}n (5). Single-crystal X-ray diffraction on 1–5 reveals that they crystallize in the triclinic system, P1 space group with the series 1–4 being isostructural. The crystal structure of the five compounds are 3D with the lanthanide(III) ions linked through 2,5-pzdc2– dianions acting as two- and fourfold connectors, buildi…

BinodalLanthanidePhotoluminescence010405 organic chemistryChemistryInorganic chemistryCrystal structureTriclinic crystal system010402 general chemistry01 natural sciences0104 chemical sciencesInorganic ChemistryCrystallographyHydrothermal synthesisPhysical and Theoretical ChemistryIsostructuralLuminescenceInorganic Chemistry
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ChemInform Abstract: Combinatorial Biosynthesis of Polyketides

2010

BiochemistryChemistryCombinatorial biosynthesisGeneral MedicineChemInform
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The role of size and protein shells in the toxicity to algal photosynthesis induced by ionic silver delivered from silver nanoparticles

2019

Abstract Because of their biocide properties, silver nanoparticles (AgNPs) are present in numerous consumer products. The biocidal properties of AgNPs are due to both the interactions between AgNP and cell membranes and the release of dissolved silver (Ag+). Recent studies emphasized the role of different nanoparticle coatings in complexing and storing Ag+. In this study, the availability of dissolved silver in the presence of algae was assessed for three AgNPs with different silver contents (59%, 34% and 7% of total Ag), silver core sizes and casein shell thicknesses. The impact of ionic silver on the photosynthetic yield of Chlamydomonas reinhardtii was used as a proxy to estimate the amo…

BiocideSilverEnvironmental Engineering010504 meteorology & atmospheric sciencesBiological AvailabilityMetal NanoparticlesNanoparticleIonic bonding010501 environmental sciencesProtective AgentsPhotosynthesis01 natural sciencesSilver nanoparticleNanomaterialsEnvironmental ChemistryCysteinePhotosynthesisWaste Management and Disposal0105 earth and related environmental sciencesEC50IonsDose-Response Relationship DrugChemistryPollutionMembraneChlamydomonas reinhardtiiNuclear chemistryScience of The Total Environment
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Biotechnology of Rhodococcus for the production of valuable compounds

2020

Abstract Bacteria belonging to Rhodococcus genus represent ideal candidates for microbial biotechnology applications because of their metabolic versatility, ability to degrade a wide range of organic compounds, and resistance to various stress conditions, such as metal toxicity, desiccation, and high concentration of organic solvents. Rhodococcus spp. strains have also peculiar biosynthetic activities that contribute to their strong persistence in harsh and contaminated environments and provide them a competitive advantage over other microorganisms. This review is focused on the metabolic features of Rhodococcus genus and their potential use in biotechnology strategies for the production o…

BioconversionSiderophoreBioflocculantsBioconversionMicroorganismBiosynthesiIndustrial WasteSiderophoresBiosynthesisApplied Microbiology and BiotechnologyRhodococcus Antimicrobials Bioflocculants Biosynthesis Bioconversion Biosurfactants Carotenoids Lipids Metal-based nanostructures SiderophoresBioproductsRhodococcusTriglyceridesCarotenoidHigh concentrationbiologyAntimicrobialsChemistrybusiness.industryMetal-based nanostructureBiosurfactantBioflocculantGeneral MedicineMini-ReviewLipidbiology.organism_classificationCarotenoidsLipidsRefuse DisposalBiotechnologyBiosurfactantsbacteriaAntimicrobialbusinessRhodococcusMetal-based nanostructuresBacteriaRhodococcuBiotechnologyWaste disposalApplied Microbiology and Biotechnology
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Microbiological transformations. 30. Enantioselective hydrolysis of racemic epoxides: the synthesis of enantiopure insect juvenile hormone analogs (b…

1993

Abstract The enantioselective epoxide biohydrolysis of the racemic benzodioxole 6,7-epoxygeraniol derivative 1 has been achieved using the fungus A. niger . This new type of preparative scale bioconversion allows the synthesis of both enantiomers of Bower's compound, an analogue of insect juvenile hormone. Biological tests showed that the 6(R) enantiomer was about ten times more active than the 6(S) enantiomer against the yellow meal worm Tenebrio molitor .

BioconversionStereochemistryOrganic ChemistryEnantioselective synthesisEpoxideCatalysisCompound sInorganic Chemistrychemistry.chemical_compoundEnantiopure drugchemistryJuvenile hormoneOrganic chemistryPhysical and Theoretical ChemistryEnantiomerDerivative (chemistry)Tetrahedron: Asymmetry
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Study of Epitope Imprinting for Small Templates: Preparation of NanoMIPs for Ochratoxin A

2019

BiomaterialsOchratoxin Achemistry.chemical_compoundSolid-phase synthesisTemplateRenewable Energy Sustainability and the EnvironmentChemistryMaterials ChemistryEnergy Engineering and Power TechnologyImprinting (psychology)Surface plasmon resonanceCombinatorial chemistryEpitopeChemNanoMat
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