Publications by authors named "Tommaso Fantoni"

Article Synopsis
  • - Fluorine-containing molecules are becoming more common in pharmaceuticals and other applications, with the cyanodifluoromethyl group being notable for its size and distinct electronic properties compared to the trifluoromethyl group.
  • - The synthesis of cyanodifluoromethyl compounds is complex, requiring multiple steps and reactive reagents, but this research introduces a copper-mediated method that simplifies the process using TMSCFCN.
  • - This new method is versatile, allowing late-stage modifications of complex molecules, and the reaction mechanism has been studied to confirm the feasibility of the process, yielding important pharmaceutical analogues.
View Article and Find Full Text PDF

The enantioselective 1,3-dipolar cycloaddition of nitrones and arylpropionaldehydes to generate highly functionalized scaffolds for application in drug discovery was herein investigated. The use of a second-generation MacMillan catalyst as hydrochloride salt consistently accelerated the reaction speed, allowing a decrease in the reaction time up to >100 times, still affording 4-isoxazolines with good to excellent enantiomeric ratios at room temperature. As a proof of concept, further functionalization of the isoxazoline core through Pd-catalyzed cross-coupling was performed, generating differently functionalized chemical architectures in high yield.

View Article and Find Full Text PDF

Targeting protein-protein interactions (PPIs) has been recently recognized as an emerging therapeutic approach for several diseases. Up today, more than half a million PPI dysregulations have been found to be involved in pathological events. The dynamic nature of these processes and the involvement of large protein surfaces discouraged anyway the scientific community in considering them promising therapeutic targets.

View Article and Find Full Text PDF

The identification of a green, versatile, user-friendly, and efficient methodology is necessary to facilitate the use of Heck-Cassar-Sonogashira (HCS) cross-coupling reaction in drug discovery and industrial production in the pharmaceutical segment. The Heck-Cassar and Sonogashira protocols, using N-hydroxyethylpyrrolidone (HEP)/water/N,N,N',N'-tetramethyl guanidine (TMG) as green solvent/base mixture and sulfonated phosphine ligands, allowed to recycle the catalyst, always guaranteeing high yields and fast conversion under mild conditions, with aryl iodides, bromides, and triflates. No catalyst leakage or metal contamination of the final product were observed during the HCS recycling.

View Article and Find Full Text PDF