Alessia Ciogli


Titolo Pubblicato in Anno
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
First-in-Class Inhibitors of the Ribosomal Oxygenase MINA53 JOURNAL OF MEDICINAL CHEMISTRY 2021
On-Column Quantification of Amino Functionalities Bonded to Solid Porous Matrices Packed within High Performance Liquid Chromatography Columns JOURNAL OF CHROMATOGRAPHY A 2021
Synthesis and Characterization of Mitochondria-Targeted Triphenylphosphonium Bolaamphiphiles Mitochondrial Medicine 2021
Ultra-high performance separation of basic compounds on reversed-phase columns packed with fully/superficially porous silica and hybrid particles by using ultraviolet transparent hydrophobic cationic additives JOURNAL OF SEPARATION SCIENCE 2020
Sulfonamide inhibitors of beta-Catenin signaling as anticancerAgents with different output on c-Myc CHEMMEDCHEM 2020
Molecular Recognition of the HPLC Whelk-O1 Selector towards the Conformational Enantiomers of Nevirapine and Oxcarbazepine INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES 2020
Development of alkyl glycerone phosphate synthase inhibitors: Structure-activity relationship and effects on ether lipids and epithelial-mesenchymal transition in cancer cells EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY 2019
A silica-supported catalyst containing 9-amino-9-deoxy-9-epi-quinine and a benzoic acid derivative for stereoselective batch and flow heterogeneous reactions EUROPEAN JOURNAL OF ORGANIC CHEMISTRY 2019
Modular and conservative procedure for the quantification of amino functionalities bonded to solid porous matrices ANALYTICA CHIMICA ACTA 2019
An innovative method for quantification of basic sites linked on solid matrices Book of abstracts Merck Young Chemists’ Symposium XIX edition 2019
Synthesis of pyrano[2,3-: F] chromen-2-ones vs. pyrano[3,2-g] chromen-2-ones through site controlled gold-catalyzed annulations ORGANIC & BIOMOLECULAR CHEMISTRY 2019
Chemical, computational and functional insights into the chemical stability of the Hedgehog pathway inhibitor GANT61 JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY 2018
Enantioselective ultra high performance liquid and supercritical fluid chromatography: the race to the shortest chromatogram JOURNAL OF SEPARATION SCIENCE 2018
Recognition mechanism of aromatic derivatives resolved by argentation chromatography: The driving role played by substituent groups ANALYTICA CHIMICA ACTA 2018


  • PE4_5
  • PE4_10
  • PE5_17


  • 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. 



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

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