Search results for "SELECTIVITY"

showing 10 items of 1148 documents

2014

Carbon-centered radicals represent highly useful reactive intermediates in organic synthesis. Their nucleophilic character is reflected by fast additions to electron deficient C=X double bonds as present in iminium ions or cationic heterocycles. This review covers diverse reactions of preformed or in situ-generated cationic substrates with various types of C-radicals, including alkyl, alkoxyalkyl, trifluoromethyl, aryl, acyl, carbamoyl, and alkoxycarbonyl species. Despite its high reactivity, the strong interaction of the radical’s SOMO with the LUMO of the cation frequently results in a high regioselectivity. Intra- and intermolecular processes such as the Minisci reaction, the Porta react…

Addition reactionChemistryOrganic ChemistryReactive intermediateCationic polymerizationPharmaceutical ScienceIminiumRegioselectivityPhotoredox catalysisPhotochemistryMedicinal chemistryAnalytical ChemistryNucleophileChemistry (miscellaneous)Drug DiscoveryMolecular MedicinePhysical and Theoretical ChemistryMinisci reactionMolecules
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ChemInform Abstract: Radical Addition to Iminium Ions and Cationic Heterocycles

2015

Carbon-centered radicals represent highly useful reactive intermediates in organic synthesis. Their nucleophilic character is reflected by fast additions to electron deficient C=X double bonds as present in iminium ions or cationic heterocycles. This review covers diverse reactions of preformed or in situ-generated cationic substrates with various types of C-radicals, including alkyl, alkoxyalkyl, trifluoromethyl, aryl, acyl, carbamoyl, and alkoxycarbonyl species. Despite its high reactivity, the strong interaction of the radical’s SOMO with the LUMO of the cation frequently results in a high regioselectivity. Intra- and intermolecular processes such as the Minisci reaction, the Porta react…

Addition reactionNucleophileChemistryReactive intermediateCationic polymerizationPhotoredox catalysisIminiumRegioselectivityGeneral MedicineMedicinal chemistryMinisci reactionChemInform
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ChemInform Abstract: Stereoselective Nucleophilic Addition Reactions of Reactive Pseudopeptides.

2010

Addition reactionNucleophilic additionChemistryStereoselectivityGeneral MedicineCombinatorial chemistryChemInform
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Highly stereoselective tandem aza-Michael addition-enolate protonation to form partially modified retropeptide mimetics incorporating a trifluoroalan…

2003

Addition reactionTandemChemistryStereochemistryPeptidomimeticMichael reactionStereoselectivityProtonationGeneral MedicineGeneral ChemistrySolvent effectsCatalysisAngewandte Chemie (International ed. in English)
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1,4-regioselective iodofunctionalizations of 1,3-butadiene

1988

Abstract Addition reactions of benzene and acetonitrile to 1,3-butadiene are described. This new iodofunctionalization process proceeds “via” iodonium ion-allylic cation equilibrium and gives regioselectively 1,4-adducts, which can be alternatively obtained by acid treatment of the 1,2-derivative 8 .

Addition reactionchemistry.chemical_compoundchemistryOrganic ChemistryDrug DiscoveryRegioselectivityOrganic chemistry13-ButadieneAcid treatmentBenzeneAcetonitrileBiochemistryTetrahedron Letters
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Mono- and Multi-Layers

2006

Thin films incorporating or consisting of calixarenes have been widely investigated. The capacity of such films to adsorb both ions and neutral species has engendered particular interest in their use in sensor devices. Semiconductors, non-linear optical and pyroelectric materials or switchable systems for data storage are further examples of their potential use [1]. Both monoand multi-layer films can be formed from calixarenes and resorcarenes, using a variety of techniques. This chapter deals with the fundamental basis of calixarene thin film applications, including film formation and characterisation as well as studies of selectivity in small molecule interactions. Real and potential appl…

AdsorptionMaterials scienceCalixareneMonolayerMoleculeQuartz crystal microbalanceNeutron reflectometryThin filmSelectivityCombinatorial chemistry
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Noninvasive double confirmation of cocaine abuse.

2013

A double confirmation procedure, based on the combined application of Ion Mobility Spectrometry (IMS) and Infrared Spectroscopy (IR), has been developed for the noninvasive unambiguous identification of cocaine consume. The use of nasal mucus as a biological specimen for cocaine abuse confirmation has been proposed as an alternative to the use of blood and urine due to its noninvasive character and the presence of the parent compound instead of its metabolites. Sampling conditions, interferences caused by cutting agents and other substances, and limits of identification (LOI) and confirmation (LOC) have been deeply evaluated. The procedure combines the high sensitivity of the IMS to identif…

AdultMaleChromatographyChemistryIon-mobility spectrometryHigh selectivityAnalytical chemistryAnalytical ChemistrySubstance Abuse DetectionBiological specimenCocaine-Related DisordersMucusNasal MucosaCocaineNasal mucusSpectroscopy Fourier Transform InfraredHumansFemaleCocaine abuseAnalytical chemistry
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Selective Introduction of Acid Sites in Different Confined Positions in ZSM-5 and Its Catalytic Implications

2018

Controlling the location of acid sites in zeolites can have a great effect on catalysis. In this work we face the objective of directing the location of Al into the 10R channels of ZSM-5 by taking advantage of the structural preference of B to occupy certain positions at the channel intersections, as suggested by theoretical calculations. The synthesis of B-Al-ZSM-5 zeolites with variable Si/Al and Si/B ratios, followed by B removal in a postsynthesis treatment, produces ZSM-5 samples enriched in Al occupying positions at 10R channels. The location of the acid sites is determined on the basis of the product distribution of 1-hexene cracking as a test reaction. The higher selectivity to prop…

Al siting02 engineering and technology010402 general chemistryFluid catalytic cracking01 natural sciencesDFTCatalysisCatalysisPropenechemistry.chemical_compoundQUIMICA ORGANICABoron ZSM-5General Chemistry021001 nanoscience & nanotechnologyProduct distribution0104 chemical sciencesCrystallographyCrackingchemistryCatalytic crackingZeolitesMethanolZSM-5MTO0210 nano-technologySelectivityACS Catalysis
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Stereocontrolled synthesis of D-α-hydroxy carboxylic acid from L-amino acids

1987

Abstract Optically active D-α-hydroxy carboxylic acids are obtained from L-amino acids via L-α-halocarboxylic acids and their stereoselective reaction with cesium p-nitrobenzoate.

Alaninechemistry.chemical_classificationChemistryStereochemistryCarboxylic acidOrganic ChemistryPhenylalanineBiochemistryAmino acidValineDrug DiscoveryOrganic chemistryStereoselectivityLeucineAliphatic compoundTetrahedron Letters
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Tuning The Selectivity To Aldehyde Via Ph Regulation In The Photocatalytic Oxidation Of 4-Methoxybenzyl Alcohol And Vanillyl Alcohol By Tio2 Catalysts

2021

Abstract The influence of pH on the photocatalytic partial oxidation of 4-methoxybenzyl alcohol (MBA) and vanillyl alcohol (VA) to their corresponding aldehydes in aqueous suspension under UVA irradiation was investigated by using poorly crystalline home-prepared and crystalline commercial TiO2 (BDH, Merck and Degussa P25) photocatalysts. The results clearly show as tuning pH can strongly impart selectivity and activity to photocatalytic processes which are often quite unselective in aqueous suspensions. It was found that pH effect on reaction rate and product selectivity strongly depended on TiO2 crystallinity and substrate type. In the case of MBA oxidation, photoreactivity and selectivit…

Alcohol02 engineering and technology010501 environmental sciences01 natural sciencesAldehydeGreen synthesis p-Anisaldehyde pH effect Photocatalysis TiO2 VanillinCatalysisVanillyl alcoholchemistry.chemical_compoundChemical Engineering (miscellaneous)Partial oxidationWaste Management and Disposal0105 earth and related environmental scienceschemistry.chemical_classificationSettore ING-IND/24 - Principi Di Ingegneria ChimicaAqueous solutionProcess Chemistry and Technology021001 nanoscience & nanotechnologyPollutioneye diseaseschemistryPhotocatalysissense organsSettore CHIM/07 - Fondamenti Chimici Delle Tecnologie0210 nano-technologySelectivityNuclear chemistry
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