scispace - formally typeset
M

Maria A. Chiacchio

Researcher at University of Catania

Publications -  87
Citations -  1118

Maria A. Chiacchio is an academic researcher from University of Catania. The author has contributed to research in topics: Catalysis & Cycloaddition. The author has an hindex of 18, co-authored 82 publications receiving 905 citations.

Papers
More filters
Journal ArticleDOI

Synthesis and biological activity of isoxazolidinyl polycyclic aromatic hydrocarbons: potential DNA intercalators.

TL;DR: In particular, compounds 7c and 7e show high levels of cytotoxicity on MOLT-3 leukemia cells; 7e exerts a remarkable enhancing activity on apoptosis caused by anti-fas antibody addition.
Journal ArticleDOI

Synthesis and biological activity of phosphonated nucleosides: part 1. Furanose, carbocyclic and heterocyclic analogues.

TL;DR: Phosphonated nucleosides represent a promising alternative in the improvement of the biological activity of nucleoside analogues in antiviral and anticancer chemotherapy.
Journal ArticleDOI

Antiviral activity of seed extract from Citrus bergamia towards human retroviruses

TL;DR: The protective effect of BSext and of the purified products was associated with the inhibition of both HTLV-1 and HIV-1 RT activities in conceptually similar, cell-free assays, showing a favourable selectivity index for the novel BSext product.
Journal ArticleDOI

Pyridine and Pyrimidine Derivatives as Privileged Scaffolds in Biologically Active Agents

TL;DR: The aim of this review is to describe the most recent reports in this field, with reference to the new discovered pyridine- or pyrimidine-based drugs, to their synthesis and to the evaluation of the most biologically active derivatives.
Journal ArticleDOI

Thermal degradation of differently substituted Cyclopentyl Polyhedral Oligomeric Silsesquioxane (CP-POSS) nanoparticles

TL;DR: In this paper, seven substituted derivatives of polyhedral oligomeric silsesquioxanes (POSSs) with general formula R7R′1 (SiO1.5)8, where R- and R′- were a cyclopentyl and a substituted phenyl group, respectively, were prepared, and their compositions were checked by elemental analysis, 1H NMR and 13C NMR spectroscopy.