Search results for "symmetrization"

showing 7 items of 37 documents

Stereoselective Synthesis of Enantiomerically Pure Piperidine Derivatives byN-Galactosylation of Pyridones

2004

Stereoselective desymmetrization of 4-pyridone has been achieved through selective N-galactosylation, activation of the N-(galactosyl)pyridone by O-silylation and immediate addition of Grignard compounds. Chiral piperidine derivatives, e.g. (S)-(+)-coniine and (5S,9S)-(+)-indolozidine 167B, were synthesised in enantiomerically pure form using these highly regio- and stereoselective reactions. After N-galactosylation of 2-pyridone and O-silylation of the N-galactosyl-2-pyridone, addition of a Grignard compound proceeded with high 1,4-regioselectivity and complete diastereoselectivity, to furnish 4-substituted 5,6-dehydro-2-piperidones. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Ger…

chemistry.chemical_compoundChemistryStereochemistryOrganic ChemistryOrganic chemistryStereoselectivityPiperidinePhysical and Theoretical ChemistryDesymmetrizationEuropean Journal of Organic Chemistry
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Stereoselective Synthesis of Enantiomerically Pure Piperidine Derivatives by N-Galactosylation of Pyridones.

2004

Stereoselective desymmetrization of 4-pyridone has been achieved through selective N-galactosylation, activation of the N-(galactosyl)pyridone by O-silylation and immediate addition of Grignard compounds. Chiral piperidine derivatives, e.g. (S)-(+)-coniine and (5S,9S)-(+)-indolozidine 167B, were synthesised in enantiomerically pure form using these highly regio- and stereoselective reactions. After N-galactosylation of 2-pyridone and O-silylation of the N-galactosyl-2-pyridone, addition of a Grignard compound proceeded with high 1,4-regioselectivity and complete diastereoselectivity, to furnish 4-substituted 5,6-dehydro-2-piperidones. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Ger…

chemistry.chemical_compoundStereochemistryChemistryStereoselectivityGeneral MedicinePiperidineDesymmetrizationChemInform
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ChemInform Abstract: Desymmetrization Reactions on 4-Pyridone Using Carbohydrate Templates.

2010

chemistry.chemical_compoundTemplatechemistryOrganic chemistryGeneral MedicineCarbohydrate4-PyridoneDesymmetrizationChemInform
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Molecular mechanics models for the image charge, a comment on “including image charge effects in the molecular dynamics simulations of molecules on m…

2017

We re-investigate the image charge model of Iori and Corni (Iori and Corni, J. Comput. Chem. 2008, 29, 1656). We find that a simple symmetrization of their model allows to obtain quantitatively correct results for the electrostatic interaction of a water molecule with a metallic surface. This symmetrization reduces the magnitude of the electrostatic interaction to less than 10% of the total interaction energy. © 2017 Wiley Periodicals, Inc.

image chargewatermetal surface010402 general chemistryMethod of image charges01 natural sciencesMolecular physicsMolecular mechanics[ CHIM ] Chemical SciencesForce field (chemistry)MetalMolecular dynamicsTheoretical and Computational ChemistryQuantum mechanics0103 physical sciencesMolecule[CHIM]Chemical SciencesChemical Physics010304 chemical physicsChemistryforce fieldGeneral ChemistryInteraction energy0104 chemical sciencesComputational Mathematicsadsorptionvisual_artvisual_art.visual_art_mediumSymmetrizationPhysical Chemistry (incl. Structural)
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Comparison results for a linear elliptic equation with mixed boundary conditions

2003

In this paper we study a linear elliptic equation having mixed boundary conditions, defined in a connected open set $\Omega $ of $\mathbb{R}^{n}$. We prove a comparison result with a suitable ``symmetrized'' Dirichlet problem which cannot be uniformly elliptic depending on the regularity of $ \partial \Omega $. Regularity results for non-uniformly elliptic equations are also given.

symmetrization35B6535J25Settore MAT/05 - Analisi MatematicaApplied Mathematics35B05Comparison result35J70Analysis
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Monge-Ampere type equations: Comparative results

2003

Summary of the PhD thesis

symmetrizationSettore MAT/05 - Analisi MatematicaMonge-Ampère equation
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Desymmetrization of Prochiral Cyclobutanones via Nitrogen Insertion: A Concise Route to Chiral γ‐Lactams

2021

Abstract Asymmetric access to γ‐lactams is achieved via a cyclobutanone ring expansion using widely available (1S,2R)‐1‐amino‐2‐indanol for chiral induction. Mechanistic analysis of the key N,O‐ketal rearrangement reveals a Curtin–Hammett scenario, which enables a downstream stereoinduction (up to 88:12 dr) and is corroborated by spectroscopic, crystallographic, and computational studies. In combination with an easy deprotection protocol, this operationally simple sequence allows the synthesis of a range of optically pure γ‐lactams, including those bearing all‐carbon quaternary stereocenters. In addition, the formal synthesis of drug molecules baclofen, brivaracetam, and pregabalin further …

γ-lactamsChiral auxiliary010405 organic chemistryChemistryasymmetric synthesisEnantioselective synthesisCyclobutanoneGeneral Chemistry010402 general chemistryRing (chemistry)01 natural sciencesCombinatorial chemistryDesymmetrizationCatalysis0104 chemical sciencesStereocenterdesymmetrizationFormal synthesischemistry.chemical_compoundMoleculecyclobutanoneResearch ArticlesResearch ArticleAsymmetric Synthesis | Hot PaperAngewandte Chemie International Edition
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