Accueil › Annuaire des chercheurs › Moheddine Askri
Moheddine Askri
Affiliation : University of Monastir
- 35Publications (affiliation tunisienne)
- 84Publications au total
- 896Citations
- 15Indice h
Profil de recherche
Moheddine Askri compte 35 publications référencées (2007–2022). Ses travaux paraissent principalement dans « ChemInform », « HAL » et « RSC Advances ». Son article le plus cité, « Synthesis, antidiabetic activity and molecular docking study of rhodanine-substitued spirooxindole pyrrolidine derivatives as novel α-amylas » (2020), a été cité 133 fois. 6 de ces publications datent des trois dernières années d’activité. Ses travaux sont cosignés avec au moins 12 chercheurs, notamment dans des établissements de France, Canada, Arabie saoudite.
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Créer mon profil gratuit Ajouter mes publicationsDomaines de recherche
- Crystal structures of chemical compounds
- Crystallography and molecular interactions
- Crystal Structures and Properties
- Multicomponent Synthesis of Heterocycles
- Organic Chemistry Cycloaddition Reactions
Publications (35)
- Antimicrobial Activity and DFT Studies of a Novel Set of Spiropyrrolidines Tethered with Thiochroman-4-one/Chroman-4-one Scaffolds
- New spiropyrrolothiazole derivatives bearing an oxazolone moiety as potential antidiabetic agent: Design, synthesis, crystal structure, Hirshfeld surface analysis, ADME and molecular docking studies
- Chemoselective and diastereodivergent synthesis of new spirooxindolo-pyrrolizidines and pyrrolidines stemming from unsymmetrical 1,3-bis(arylidene)tetral-2-ones: a combined experimental and theoretical study
- Diversity-Oriented Synthesis of Spiropyrrolo[1,2- a ]isoquinoline Derivatives via Diastereoselective and Regiodivergent Three-Component 1,3-Dipolar Cycloaddition Reactions: In Vitro and in Vivo Evaluation of the Antidiabetic Activity of Rhodanine Analogues
- Synthesis, antidiabetic activity and molecular docking study of rhodanine-substitued spirooxindole pyrrolidine derivatives as novel α-amylase inhibitors
- Three-Component Access to Functionalized Spiropyrrolidine Heterocyclic Scaffolds and Their Cholinesterase Inhibitory Activity
- Highly diastereoselective construction of novel dispiropyrrolo[2,1- a ]isoquinoline derivatives via multicomponent 1,3-dipolar cycloaddition of cyclic diketones-based tetrahydroisoquinolinium N -ylides
- Straightforward and Highly Diastereoselective Synthesis of a New Set of Functionalized Dispiropyrrolidines Involving Multicomponent 1,3‐Dipolar Cycloaddition with Azomethine Ylides
- Visible-light-mediated α-phosphorylation of N -aryl tertiary amines through the formation of electron-donor–acceptor complexes: synthetic and mechanistic studies
- One-pot four-component domino strategy for the synthesis of novel spirooxindole–pyrrolidine/pyrrolizidine-linked 1,2,3-triazole conjugates via stereo- and regioselective [3+2] cycloaddition reactions: In vitro antibacterial and antifungal studies
- Synthesis of New Spirooxindole‐Fused Isoxazoline/Triazole and Isoxazoline/Isoxazole Derivatives from Three‐Component 1,3‐Dipolar Cycloaddition
- Stoichiometry-controlled cycloaddition of nitrilimines with unsymmetrical exocyclic dienones: microwave-assisted synthesis of novel mono- and dispiropyrazoline derivatives
- Bis{(4-methylthio)phenylthio}methane as assembling ligand for the construction of Cu(I) and Hg(II) coordination polymers. Crystal structures and topological (AIM) analysis of the bonding
- Regioselective Synthesis of Mono‐ and Dispiropyrazoline Derivatives via 1,3‐dipolar Cycloaddition with Nitrilimines
- Crystal structure of 4,4-dibromo-1-(3,4-dimethoxyphenyl)-2-azabuta-1,3-diene-1-carbonitrile
- ChemInform Abstract: Synthesis of New Spirooxindole Derivatives Through 1,3‐Dipolar Cycloaddition of Azomethine Ylides and Their Antitubercular Activity.
- ChemInform Abstract: Design of Novel Dispirooxindolopyrrolidine and Dispirooxindolopyrrolothiazole Derivatives as Potential Antitubercular Agents.
- ChemInform Abstract: Regio‐ and Stereoselective Synthesis of Spiropyrrolizidines and Piperazines Through Azomethine Ylide Cycloaddition Reaction.
- ChemInform Abstract: Stoichiometry‐Controlled Cycloaddition of Nitrilimines with Unsymmetrical Exocyclic Dienones: Microwave‐Assisted Synthesis of Novel Mono‐ and Dispiropyrazoline Derivatives.
- Regio- and Stereoselective Synthesis of Spiropyrrolizidines and Piperazines through Azomethine Ylide Cycloaddition Reaction
- Synthesis of new spirooxindole derivatives through 1,3-dipolar cycloaddition of azomethine ylides and their antitubercular activity
- Design of novel dispirooxindolopyrrolidine and dispirooxindolopyrrolothiazole derivatives as potential antitubercular agents
- Synthesis of highly substituted spiropyrrolidines via 1, 3-dipolar cycloaddition reaction of N-metalated azomethine ylides. A new access to spiropyrrolines derivatives
- ChemInform Abstract: Synthesis of Novel Dispiropyrrolothiazoles by Three‐Component 1,3‐Dipolar Cycloaddition and Evaluation of Their Antimycobacterial Activity.
- A strategic approach to the synthesis of functionalized spirooxindole pyrrolidine derivatives: in vitro antibacterial, antifungal, antimalarial and antitubercular studies
- Synthesis of novel dispiropyrrolothiazoles by three-component 1,3-dipolar cycloaddition and evaluation of their antimycobacterial activity
- ÉTUDE DE LA RÉACTION DE CYCLOADDITION DIPOLAIRE-1,3 DES YLURES D'AZOMÉTHINE N-MÉTALLES SUR LES 3-ARYLIDÈNE-1-PHÉNYLPYRROLIDINE- 2,5-DIONES
- Synthèse et Réactivité de 2-Azabutadiènes Fonctionnalisés - 17èmes journées de Société Chimique de Tunisie, JNC
- Synthèse et Réactivité de 2-Azabutadiènes Fonctionnalisés. Applications en Chimie de Coordination Organométallique 17 èmes journées de Société Chimique de Tunisie, JNC
- Synthesis, structure and luminescence properties of new spiro-heterocyclic pyrrolidine and 3,4-dihydro-3H-pyrrole derivative
- ChemInform Abstract: An Efficient One Pot Synthesis of New Indanopyrazoline and Indanopyrazole Derivatives.
- 1,3-Dipolar cycloaddition of diarylnitrilimines with some enones bearing an exo or endo cyclic conjugated doubel bond
- Synthèse de composés hétérocycliques de type arylnaphtaléno-(1,2-d) isoxazole par cycloaddition 1,3-dipolaire d'arylnitriloxydes sur des énamines d'a-tétralone
- Spiroheterocycles from the Reaction of Arylnitrile Oxides with Some (Z)-3-Arylidene-2(3H)-benzofuranones. New Access to Orthohydroxyphenylisoxazoline Esters
- Synthesis of Some Spirochroman‐4‐ones by Regioselective [4 + 2] Cycloaddition Reactions.
Revues de publication
- ChemInform × 7
- HAL × 6
- RSC Advances × 3
- Journal of Heterocyclic Chemistry × 3
- Molecules × 2
- New Journal of Chemistry × 2
Publications par année
- 20223
- 20211
- 20202
- 20192
- 20182
- 20171
- 20168
- 20155
- 20142
- 20131
Collaborations
Établissements partenaires : Université de Sherbrooke · Centre National de la Recherche Scientifique · Centre québécois sur les matériaux fonctionnels · Qassim University · University of Ha'il
Pays des co-auteurs : France · Canada · Arabie saoudite
Co-auteurs
- Sarra Boudriga
- Saoussen Haddad
- Fadwa Rouatbi
- Michael Knorr
- Carsten Strohmann B
- Chourouk Mhiri
- Yoann Rousselin
- Marek M. Kubicki
- Dharmarajan Sriram
- Khaled Hamden
- Christopher Golz
- Perumal Yogeeswari
Données bibliographiques issues d’OpenAlex (base ouverte).
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