Alessia Ciogli

Pubblicazioni

Titolo Pubblicato in Anno
Systematic Design of Adenosine Analogs as Inhibitors of a Clostridioides difficile-Specific DNA Adenine Methyltransferase Required for Normal Sporulation and Persistence JOURNAL OF MEDICINAL CHEMISTRY 2023
Diaryl-Pyrano-Chromenes Atropisomers: Stereodynamics and Conformational Studies MOLECULES 2023
Enantioselective catalytic Strecker reaction on cyclic (Z)-aldimines in flow: reaction optimization and sustainability aspects JOURNAL OF FLOW CHEMISTRY 2023
Primary amine catalyzed activation of carbonyl compounds: a study on reaction pathways and reactive intermediates by mass spectrometry EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2022
Resveratrol loaded in cationic glucosylated liposomes to treat Staphylococcus epidermidis infections CHEMISTRY AND PHYSICS OF LIPIDS 2022
A perspective on enantioselective chromatography by comparing ultra-high performance supercritical fluid chromatography and normal-phase liquid chromatography through the use of a Pirkle-type stationary phase TRAC. TRENDS IN ANALYTICAL CHEMISTRY 2022
Valorization of By-Products from Biofuel Biorefineries: Extraction and Purification of Bioactive Molecules from Post-Fermentation Corn Oil FOODS 2022
Accelerated D‑Fructose acid-catalyzed reactions in thin films formed by charged microdroplets deposition JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY 2022
Effect of natural deep eutectic solvents on trans-resveratrol photo-chemical induced isomerization and 2,4,6-trihydroxyphenanthrene electro-cyclic formation MOLECULES 2022
Preparation of a high-density vinyl silica gel to anchor cysteine via photo-click reaction and its applications in hydrophilic interaction chromatography JOURNAL OF CHROMATOGRAPHY A 2022
Novel Insights on Human Carbonic Anhydrase Inhibitors Based on Coumalic Acid: Design, Synthesis, Molecular Modeling Investigation, and Biological Studies INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES 2022
Synthesis of Atropisomeric Hydrazides by One‐Pot Sequential Enantio‐ and Diastereoselective Catalysis ANGEWANDTE CHEMIE. INTERNATIONAL EDITION 2022
A Compendium of the Principal Stationary Phases Used in Hydrophilic Interaction Chromatography: Where Have We Arrived? SEPARATIONS 2022
Induction of Ferroptosis in Glioblastoma and Ovarian Cancers by a New Pyrrole Tubulin Assembly Inhibitor JOURNAL OF MEDICINAL CHEMISTRY 2022
Asymmetric Hydroarylation Reactions Catalyzed by Transition Metals: Last 10 Years in a Mini Review CATALYSTS 2022
Reactivity of Indolylmethylacetates with N, O, and S Soft Nucleophiles: Evidence of 2-Alkylideneindolenines and 3-Alkylideneindoleninium Generation by ESI-MS and IRMPD Spectroscopy EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2022
Static vs. Dynamic Electrostatic Repulsion Reversed Phase Liquid Chromatography: Solutions for Pharmaceutical and Biopharmaceutical Basic Compounds SEPARATIONS 2021
Mannosyl, glucosyl or galactosyl liposomes to improve resveratrol efficacy against Methicillin Resistant Staphylococcus aureus biofilm COLLOIDS AND SURFACES. A, PHYSICOCHEMICAL AND ENGINEERING ASPECTS 2021
Salivary caffeine in Parkinson’s disease SCIENTIFIC REPORTS 2021
Chromatographic separation of the interconverting enantiomers of imidazo- and triazole-fused benzodiazepines JOURNAL OF CHROMATOGRAPHY A 2021

ERC

  • PE4_5
  • PE4_10
  • PE5_17

KET

  • Advanced materials
  • Sustainable technologies & development

Interessi di ricerca

L’attività scientifica è focalizzata da un lato allo studio dei processi di riconoscimento molecolare mediante cromatografia liquida ad elevate prestazioni (sintesi di fasi stazionarie di nuova generazione UHPLC e sviluppo di metodi analitici avanzati); e dall’altro, sulla completa indagine stereochimica di molecole chirali sia nel campo della chimica organica che in quello biofarmaceutico con particolare attenzione allo studio di specie stereolabili. Più recente è l'interesse verso lo studio di sistemi organocatalitici per sintesi asimmetrica mediante spettrometria di massa e il loro uso in sistemi eterogenei. 

 

Keywords

enantiomer separation
high-performance liquid chromatography–tandem mass spectrometry (HPLC–MS–MS)
organocatalysis

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