M. C. Fulco

Synthesis, biological characterization and molecular modeling insights of spirochromanes as potent HDAC inhibitors.

S. Minucci, C. Mercurio, L. Moretti, 2016, European journal of medicinal chemistry.

Discovery, synthesis, and pharmacological evaluation of spiropiperidine hydroxamic acid based derivatives as structurally novel histone deacetylase (HDAC) inhibitors.

A. Mai, S. Minucci, C. Mercurio, 2011, Journal of medicinal chemistry.

Exploring the metal-catalyzed reaction of furans with alkyl α-diazomethanesulfonate and α-diazomethanephosphonate: synthesis of ω-acyl-substituted sulfono- and phosphonobutadienes

R. Pellicciari, M. Marinozzi, L. Amori, 2009 .

New one-pot synthesis of pyrazole-5-carboxylates by 1,3-dipole cycloadditions of ethyl diazoacetate with α-methylene carbonyl compounds

R. Pellicciari, F. Venturoni, A. Gioiello, 2009 .

Synthesis of Novel Unsymmetrically Bridgehead-Substituted Phenylselenobicyclo[1.1.1]pentanes.

R. Pellicciari, M. Marinozzi, R. Rizzo, 2004 .

Synthesis and chromatographic resolution of conformationally constrained analogues of homotaurine

B. Natalini, R. Pellicciari, R. Sardella, 2009 .

Synthesis, molecular modeling studies, and preliminary pharmacological characterization of all possible 2-(2'-sulfonocyclopropyl)glycine stereoisomers as conformationally constrained L-homocysteic acid analogs.

R. Pellicciari, A. Macchiarulo, C. Thomsen, 2007, Journal of medicinal chemistry.

Synthesis and Preliminary Biological Evaluation of 2′‐Substituted 2‐(3′‐Carboxybicyclo[1.1.1]pentyl)glycine Derivatives as Group I Selective Metabotropic Glutamate Receptor Ligands

B. Natalini, R. Pellicciari, A. Macchiarulo, 2006, ChemMedChem.