Search results for "Enolates"

showing 5 items of 5 documents

From over-stoichiometric to sub-stoichiometric enantioselective protonation with 2-sulfinyl alcohols: A view in perspective

2005

A general study of the enantioselective protonation of prochiral enolates with 2-sulfinyl alcohols is reported. The modification of reaction conditions to reduce drastically the amount of chiral proton source needed to obtain a good enantiomeric excess is reported. The effects of the different factors controlling the stereoselectivity are clearly established. Different protocols for enolate generation are compared. Medio Simon, Mercedes, Mercedes.Medio@uv.es ; Aleman Lopez, Pedro Antonio, Pedro.Aleman@uv.es ; Gil Tomas, Jesus Javier, Jesus.J.Gil@uv.es ; Asensio, Aguilar Gregorio, Gregorio.Asensio@uv.es

Enantioselective protonationUNESCO::QUÍMICA:QUÍMICA::Química orgánica [UNESCO]Sulfinyl alcoholsEnolatesEnolates ; Enantioselective protonation ; Sulfinyl alcoholsUNESCO::QUÍMICA::Química orgánica:QUÍMICA [UNESCO]
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Chemistry of detrifluoroacetylativelyin situgenerated fluoro-enolates

2018

This review article comprehensively profiles all literature reports (2015-2018) related to the detrifluoroacetylative in situ generation of fluorine-containing enolates and their reactions with electrophilic reagents. The innovative facets of this unconventional methodology and its synthetic generality for the preparation of fluorine-containing compounds of high medicinal value are highlighted.

In situ010405 organic chemistryChemistryOrganic Chemistry010402 general chemistryfloroorganic compound01 natural sciencesBiochemistryCombinatorial chemistryalfa-fluoroenolates0104 chemical sciencesElectrophileDetrifluoroacetylationPhysical and Theoretical ChemistryValue (mathematics)Detrifluoroacetylation floroorganic compound alfa-fluoroenolates.Organic & Biomolecular Chemistry
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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
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A DFT study of the molecular mechanisms of the nucleophilic addition of ester-derived lithium enolates and silyl ketene acetals to nitrones: Effects …

2006

9 pages, 6 schemes, 3 figures, 2 tables.

chemistry.chemical_classificationNucleophilic additionSilylationReaction mechanismsOrganic ChemistryKeteneEnolatesMedicinal chemistryCycloadditionNitroneLewis acid catalysischemistry.chemical_compoundDensity functional calculationsAcetalsNucleophilechemistryOrganic chemistryLewis acids and basesPhysical and Theoretical ChemistryNucleophilic addition
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Carboxylate catalyzed isomerization of β,γ‐unsaturated N-acetylcysteamine thioesters

2022

We demonstrate herein the capacity of simple carboxylate salts – tetrametylammonium and tetramethylguanidinium pivalate – to act as catalysts in the isomerization of β,γ-unsaturated thioesters to α,β-unsaturated thioesters. The carboxylate catalysts gave reaction rates comparable to those obtained with DBU, but with fewer side reactions. The reaction exhibits a normal secondary kinetic isotope effect ( k 1H / k 1D = 1.065±0.026) with a β,γ−deuterated substrate. Computational analysis of the mechanism provides a similar value ( k 1H / k 1D = 1.05) with a mechanism where γ-reprotonation of the enolate intermediate is rate determining. peerReviewed

thioesterskatalyytitkinetic isotope effectsisomeriakatalyysirikkiyhdisteetcarboxylatesreaction mechanismreaktiomekanismitbase catalysisisomerizationenolatesorgaaniset yhdisteet
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