Search results for "organic synthesis"

showing 10 items of 82 documents

Electrochemical Screening for Electroorganic Synthesis

2015

Electrochemical screening is usually strongly focused on electroanalytical data, while the parameters of organic synthesis are mostly not used as selection criteria. Typical parameters would be indication of the formation of the product and the efficiency of the electroorganic conversion. The latter data indicate the stability of the product under electrolysis conditions and represent the key for the accumulation of the desired product. We survey the current methods for electroorganic screening. In particular, parallel electrolysis under more defined conditions is discussed in detail since it represents a powerful tool for the development of electroorganic syntheses and processes.

Electrolysis010405 organic chemistryOrganic Chemistry010402 general chemistryElectrochemistry01 natural sciencesCombinatorial chemistry0104 chemical scienceslaw.inventionchemistry.chemical_compoundchemistrylawOrganic chemistryOrganic synthesisPhysical and Theoretical ChemistryOrganic Process Research & Development
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Solvent Control in Electro-Organic Synthesis

2018

Exploiting the solvent control within electro-organic conversions is a far underestimated parameter in prep-scale electrolysis. The beneficial application in several transformations is outlined and in particular discussed for the dehydrogenative coupling of arenes and heteroarenes. This simple electrolytic strategy in fluorinated solvents allows the modulation of the substrate’s nucleophilicity and the stabilization of the intermediates as well as of the final product from over-oxidation.1 Introduction2 Solvent Effects in Kolbe Electrolysis and Anodic Fluorination3 Unique Solvent Effects of 1,1,1,3,3,3-Hexafluoropropan-2-ol (HFIP)4 Anodic Dehydrogenative Coupling Reactions with Use of HFIP …

ElectrolysisKolbe electrolysis010405 organic chemistryChemistryOrganic Chemistry010402 general chemistryElectrosynthesis01 natural sciencesCombinatorial chemistryCoupling reactionElectrochemical fluorination0104 chemical scienceslaw.inventionSolventchemistry.chemical_compoundlawOrganic synthesisSolvent effectsSynlett
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Industrial Microreactor Process Development up to Production

2008

This chapter is about industrial applications of microprocess technology. Industry is not very active in publishing not only because of confidentiality reasons but also because of the absence of direct need for a corresponding profile. Thus, one cannot expect that the ongoing developments can be shown with a similar degree of completeness, clarity and detailedness, as this is possible for reviewing scientific contributions from academy with a wealth of peer-reviewed papers. Especially, the information of major interest of what has been transferred to production and how do the companies make profit with the new technology is usually kept secret. Thus, it has to be accepted that some informat…

EngineeringProfit (accounting)Process developmentOrganic synthesisIndustrial microreactor process developmentFine chemicals010402 general chemistry01 natural scienceslaw.inventionChemical productionlawProduction (economics)ConfidentialityMicroprocess technologybusiness.industry010405 organic chemistryData scienceManufacturing engineering0104 chemical sciencesMicroreactorOrganic catalysisPeptide synthesisWork (electrical)PublishingMicrochannelPilots plantsCLARITYScreening studies in laboratorybusinessIndustrial microreactor productionMicro Process Engineering
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Electro-organic synthesis – a 21st century technique

2020

The severe limitations of fossil fuels and finite resources influence the scientific community to reconsider chemical synthesis and establish sustainable techniques. Several promising methods have emerged, and electro-organic conversion has attracted particular attention from international academia and industry as an environmentally benign and cost-effective technique. The easy application, precise control, and safe conversion of substrates with intermediates only accessible by this method reveal novel pathways in synthetic organic chemistry. The popularity of electricity as a reagent is accompanied by the feasible conversion of bio-based feedstocks to limit the carbon footprint. Several mi…

Engineeringchemistry.chemical_compoundchemistrybusiness.industryFossil fuelCarbon footprintOrganic synthesisGeneral ChemistryBiochemical engineeringbusinessChemical Science
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Synthesis of complex organic molecules in soft x-ray irradiated ices

2019

We study the chemical evolution of H2O:CO:NH3 ice mixtures irradiated with soft X-rays, in the range 250-1250 eV. We identify many nitrogen-bearing molecules such as e.g., OCN-, NH4+ , HNCO, CH3CN, HCONH2, and NH2COCONH2. Several infrared features are compatible with glycine or its isomers. During the irradiation, we detected through mass spectroscopy many species desorbing the ice. Such findings support either the infrared identifications and reveal less abundant species with not clear infrared features. Among them, m/z = 57 has been ascribed to methyl isocyanate (CH3NCO), a molecule of prebiotic relevance, recently detected in protostellar environments. During the warm up after the irradi…

FormamidePhysicsRange (particle radiation)010504 meteorology & atmospheric sciencesInfraredAnalytical chemistryFOS: Physical sciencesAstronomy and AstrophysicsMass spectrometry01 natural sciencesAstrophysics - Astrophysics of GalaxiesStarschemistry.chemical_compoundchemistrySpace and Planetary ScienceAstrophysics of Galaxies (astro-ph.GA)0103 physical sciencesMoleculeOrganic synthesisIrradiation010303 astronomy & astrophysics0105 earth and related environmental sciences
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Electrochemical Allylic Oxidation of Olefins: Sustainable and Safe.

2016

The power you're supplying: With the application of an optimized electrochemical approach, the allylic oxidation of olefins, which is an important C-H activation process that provides access to enones, becomes a sustainable, versatile, and potent key reaction for organic synthesis.

Green chemistryAllylic rearrangement010405 organic chemistryGeneral Chemistry010402 general chemistryElectrosynthesisElectrochemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundchemistryOrganic chemistryOrganic synthesisAngewandte Chemie (International ed. in English)
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Iron-Catalyzed C−O Bond Activation: Opportunity for Sustainable Catalysis

2017

Oxygen-based electrophiles have emerged as some of the most valuable cross-coupling partners in organic synthesis due to several major strategic and environmental benefits, such as abundance and potential to avoid toxic halide waste. In this context, iron-catalyzed C-O activation/cross-coupling holds particular promise to achieve sustainable catalytic protocols due to its natural abundance, inherent low toxicity, and excellent economic and ecological profile. Recently, tremendous progress has been achieved in the development of new methods for functional-group-tolerant iron-catalyzed cross-coupling reactions by selective C-O cleavage. These methods establish highly attractive alternatives t…

Green chemistryIronGeneral Chemical EngineeringNanotechnologyContext (language use)010402 general chemistry01 natural sciencesCatalysisCatalysischemistry.chemical_compoundEnvironmental ChemistryGeneral Materials ScienceOrganic ChemicalsLow toxicity010405 organic chemistryIron catalyzedGreen Chemistry TechnologyCombinatorial chemistryCarbon0104 chemical sciencesOxygenGeneral EnergychemistrySustainabilityElectrophileOrganic synthesisChemSusChem
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Uncommon perspectives in palladium- and copper-catalysed arylation and heteroarylation of terminal alkynes following Heck or Sonogashira protocols: I…

2013

Abstract Conjugated alkynes are recurring building blocks in natural products and in a wide range of important compounds, such as pharmaceuticals, agrochemicals, or molecular materials. The palladium-catalysed cross-coupling reaction between the sp 2 -hybridized carbon atoms of aryl, heteroaryl, and vinyl halides with the sp -hybridized carbon atoms of terminal alkynes is one of the most important developments in the field of alkyne chemistry over the past 50 years. Room for improvement still exists in these important reactions of direct arylation of terminal alkynes. In this prospect, the present authors have developed several strategies aiming at improving the reactivity, the selectivity,…

Green chemistrychemistry.chemical_classificationGeneral Chemical EngineeringArylchemistry.chemical_elementAlkyneSonogashira couplingGeneral ChemistryCombinatorial chemistrychemistry.chemical_compoundchemistryIonic liquidOrganic synthesisReactivity (chemistry)PalladiumComptes Rendus Chimie
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Probing a Polar Cluster in the Retinal Binding Pocket of Bacteriorhodopsin by a Chemical Design Approach

2012

Bacteriorhodopsin has a polar cluster of amino acids surrounding the retinal molecule, which is responsible for light harvesting to fuel proton pumping. From our previous studies, we have shown that threonine 90 is the pivotal amino acid in this polar cluster, both functionally and structurally. In an attempt to perform a phenotype rescue, we have chemically designed a retinal analogue molecule to compensate the drastic effects of the T90A mutation in bacteriorhodopsin. This analogue substitutes the methyl group at position C(13) of the retinal hydrocarbon chain by and ethyl group (20-methyl retinal). We have analyzed the effect of reconstituting the wild-type and the T90A mutant apoprotein…

Halobacterium salinarumModels MolecularProtein FoldingProtein Denaturation01 natural sciencesBiotecnologiaBiochemistryBiophysics Simulationschemistry.chemical_compoundSensory RhodopsinsHalobacterium salinarum0303 health sciencesMultidisciplinarybiologyProtein StabilityQRTemperatureUltraviolet-visible spectroscopyThermal stabilityBacterial BiochemistryChemistryBiochemistryBacteriorhodopsinsRetinaldehydeMedicineProtonsResearch ArticleSteric effectsHydrogen bondingBioquímicaProtein StructureScienceRetinal bindingBiophysics010402 general chemistryMicrobiologyPhosphates03 medical and health sciencesBiology030304 developmental biologyAspartic AcidBinding SitesAdaptation OcularOrganic ChemistryOrganic SynthesisProteinsChromoproteinsRetinalBacteriorhodopsinBacteriologyBiological TransportChromophorebiology.organism_classification0104 chemical sciencesTransmembrane ProteinschemistryRetinaldehydeBiophysicsbiology.proteinMutant ProteinsPLoS ONE
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Polifunkcionālo kvaternizēto piridina atvasinājumu sintēze un īpašības

2003

Advisor: Duburs, Gunārs ; Tirzītis, Gunārs

Heterocyclic chemistryHeterocikliskie savienojumiOrganiskā ķīmija:NATURAL SCIENCES::Chemistry::Organic chemistry::Organic synthesis [Research Subject Categories]PyridinePiridīnsHeterociklu ķīmija
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