Search results for "organic reactions"

showing 4 items of 4 documents

Conformationally Locked Pyramidality Explains the Diastereoselectivity in the Methylation of trans-Fused Butyrolactones

2020

A stereoselectivity model inspired by the total synthesis of stemona alkaloids is developed to explain why enolate-derived 3,4-fused butyrolactones are methylated with a preference for syn alkylation. The model shows how conformational locking present in nonplanar enolate structures favors syn over anti methylation, due to less significant structural distortions in the syn pathway. The developed model was also successfully used to rationalize selectivities of previously documented methylation reactions. peerReviewed

StemonaLetterisomeriaStereochemistrytransition states010402 general chemistry01 natural sciencesBiochemistryenolatesheterocyclic compoundsPhysical and Theoretical Chemistryorgaaniset yhdisteetkemialliset reaktiotbiology010405 organic chemistryChemistryorganic chemicalsOrganic ChemistryselectivityTotal synthesisMethylationbiology.organism_classification0104 chemical sciencesalkaloiditchemical structureorganic reactionsStereoselectivityOrganic Letters
researchProduct

Stopped-Flow and DFT Studies of Proton Transfer and Isomerization of 5-Amino-3-imino-1,2,6,7-tetracyano-3H-pyrrolizine and Its Related Base 2-(5-Amin…

2001

International audience; A complete kinetic study of pH-dependent isomerization of 5-amino-3-imino-1,2,6,7-tetracyano-3H-pyrrolizine (HL) and 2-(5-amino-3,4-dicyano-2H-pyrrol-2-ylidene)-1,1,2-tricyanoethanide (L‘-) in the pH range from −0.5 to +13 in aqueous solution, which spans over 7 orders of magnitude for the pseudo-first-order rates (log k from −4.8 to +2.5), has revealed for the first time the existence of the corresponding conjugate species L- and HL‘. The study has allowed the determination of the acid dissociation constants of HL (pKa) and HL‘ (pKa‘), as well as all of the individual forward and reverse isomerization rates of the acidic (HL/HL‘) and basic (L-/L‘-) forms. Although L…

chemistry.chemical_classificationIsomerizationAqueous solutionBase (chemistry)ProtonStereochemistryEquilibrium[CHIM.ORGA]Chemical Sciences/Organic chemistryProtonation02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesDecompositionAcid dissociation constant0104 chemical sciences[CHIM.THEO]Chemical Sciences/Theoretical and/or physical chemistryKineticschemistryOrganic reactionsKinetic parametersPhysical and Theoretical Chemistry0210 nano-technologyIsomerizationConjugate
researchProduct

Overview on oxidation mechanisms of organic compounds by TiO2 in heterogeneous photocatalysis

2012

This review provides the reader with a general overview on heterogeneous photocatalytic oxidation mechanisms in the presence of TiO2, with a special address to conversion of aliphatic and aromatic organic species. The aim was to clarify the steps of the photo-oxidation of the various classes of compounds and to relate them with the properties of the catalysts and the experimental conditions used. Reactions carried out to perform complete degradation and photocatalytic partial oxidations have been deeply discussed. Recent isotopic studies highlighted new reaction pathways concerning partial oxidation of alcohols to aldehyde and oxidation of benzene while EPR investigations confirmed that not…

chemistry.chemical_classificationReaction mechanismRadicalOrganic ChemistryPhotochemistryAldehydeCatalysisCatalysischemistry.chemical_compoundchemistryOrganic reactionPhotocatalysisPartial oxidationSettore CHIM/07 - Fondamenti Chimici Delle TecnologiePhysical and Theoretical ChemistryPhotocatalysis Reaction mechanisms Organic reactions TiO2Benzene
researchProduct

Ionic liquids: a highway with many lanes

ionic liquids organic reactions biomass valorization ionic liquid gelsSettore CHIM/06 - Chimica Organica
researchProduct