1. “Fast, Mild, Eco-Friendly Synthesis of Polyfunctionalized Pyrroles from β-Nitroacrylates and β-Enaminones” A. Palmieri, S. Gabrielli, C. Cimarelli, R. Ballini; Green Chem. 2011, 13, 3333-3336.
2. “Solvent-free Non-Covalent Organocatalysis. Enantioselective Addition of Nitroalkanes to Alkylideneindolenines as a Flexible Gateway to Optically Active Tryptamine Derivatives” M. Fochi, L. Gramigna, S. Duce, S. Fantini, A. Palmieri, M. Petrini, L. Bernardi; Adv. Synth. Catal. 2012, 354, 1373-1380.
3. “Synthesis and Functionalization of Unsymmetrical Arylsulfonyl Bisindoles and Bisbenzazoles” S. Lancianesi, A. Palmieri, M. Petrini; Adv. Synth. Catal. 2012, 354, 3539-3544.
4. “A photochemical route to benzo[a]carbazoles via domino elimination/electrocyclization of 2-aryl-3-(1-tosylalkyl)-indoles” S. Protti, A. Palmieri, M. Petrini, M. Fagnoni, R. Ballini, A. Albini; Adv. Synth. Catal. 2013, 355, 643-646.
5. “Low Impacting Synthesis of β-Nitroacrylates under Fully Heterogeneous Conditions” A. Palmieri, S. Gabrielli, R. Ballini; Green Chem. 2013, 15, 2344-2348.
6. “Stereoselective synthesis of highly functionalized chiral 2-nitro-cyclohexane carboxylic esters via catalytic dienamine addition to α-substituted-β-nitroacrylates” E. Massolo, M. Benaglia, R. Annunziata, A. Palmieri, G. Celentano; Adv. Synth. Catal. 2014, 356, 493-500.
7. “Flow synthesis of substituted γ-lactones by consecutive photocatalytic/reductive reactions” M. Fagnoni, F. Bonassi, A. Palmieri, S. Protti, D. Ravelli, R. Ballini; Adv. Synth. Catal. 2014, 356, 753-758.
8. “Synthetic Approaches to 3-(2-Nitroalkyl) Indoles and Their Use to Access Tryptamines and Related Bioactive Compounds” S. Lancianesi, A. Palmieri, M. Petrini; Chem. Rev. 2014, 114, 7108-7149.
9. “One-pot synthesis of alkyl pyrrole-2-carboxylates starting from β-nitroacrylates and primary amines” A. Palmieri, S. Gabrielli, M. Parlapiano, R. Ballini; RSC Adv. 2015, 5, 4210-4213.
10. “Nitroaldol (Henry) reaction of 2-oxoaldehydes with nitroalkanes as a strategic step for a useful, one-pot” A. Palmieri, S. Gabrielli, S. Sampaolesi, R. Ballini; RSC Adv. 2015, 5, 36652-36655.