Research Topics
| Roberta BerniniSummaryCountry: Italy Publications
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Detail Information
Publications
Naturally occurring hydroxytyrosol: synthesis and anticancer potentialR Bernini
Universita degli Studi della Tuscia, Dipartimento di Scienze e Tecnologie per l Agricoltura, le foreste, la natura e l energia, Viterbo, Italy
Curr Med Chem 20:655-70. 2013....
A convenient and safe O-methylation of flavonoids with dimethyl carbonate (DMC)Roberta Bernini
Dipartimento di Agrobiologia e Agrochimica, Universita degli Studi della Tuscia, Via S Camillo de Lellis, 01100 Viterbo, Italy
Molecules 16:1418-25. 2011..This methylation protocol avoids the use of hazardous and high toxic reagents (diazomethane, dimethyl sulfate, methyl iodide)...
Chemoselective C-4 aerobic oxidation of catechin derivatives catalyzed by the Trametes villosa laccase/1-hydroxybenzotriazole system: synthetic and mechanistic aspectsRoberta Bernini
Dipartimento di Agrobiologia e Agrochimica, Università degli Studi della Tuscia, Viterbo, Italy
J Org Chem 76:820-32. 2011....
Synthesis of a novel ester of hydroxytyrosol and α-lipoic acid exhibiting an antiproliferative effect on human colon cancer HT-29 cellsRoberta Bernini
Dipartimento di Agrobiologia e Agrochimica, Universita degli Studi della Tuscia, Via S Camillo De Lellis snc, 01100 Viterbo, Italy
Eur J Med Chem 46:439-46. 2011..These data suggest that the novel ester might exert a more effective antitumour activity than hydroxytyrosol and α-lipoic acid...
New lipophilic piceatannol derivatives exhibiting antioxidant activity prepared by aromatic hydroxylation with 2-iodoxybenzoic acid (IBX)Roberta Bernini
Agrobiology and Agrochemistry Department, University of Tuscia, Viterbo, Italy
Molecules 14:4669-81. 2009..The new compounds showed antioxidant activity and seemed promising for possible applications as multifunctional emulsifiers in food, cosmetic and pharmaceutical fields...
A novel and efficient synthesis of highly oxidized lignans by a methyltrioxorhenium/hydrogen peroxide catalytic system. Studies on their apoptogenic and antioxidant activityRoberta Bernini
Dipartimento di Agrobiologia e Agrochimica, Universita degli Studi della Tuscia, Via S Camillo De Lellis snc, 01100 Viterbo, Italy
Bioorg Med Chem 17:5676-82. 2009..The evaluation of the antioxidant and apoptogenic activity by in vivo protocols of these compounds showed some interesting structure-activity relationships related to the oxidation degree of the molecules...
A selective de-O-methylation of guaiacyl lignans to corresponding catechol derivatives by 2-iodoxybenzoic acid (IBX). The role of the catechol moiety on the toxicity of lignansRoberta Bernini
Department of Agrobiology and Agrochemistry, University of Tuscia, 01100, Viterbo, Italy
Org Biomol Chem 7:2367-77. 2009..Thus, despite the in vitro antioxidant activity usually described for catechol derivatives, our results show for the first time the generation of a clastogenic potential, highly indicative of a long-term genetic and cancer risk...
Convenient synthesis of hydroxytyrosol and its lipophilic derivatives from tyrosol or homovanillyl alcoholRoberta Bernini
Dipartimento di Agrobiologia e Agrochimica, Universita degli Studi della Tuscia, Via S Camillo De Lellis snc, 01100 Viterbo, Italy
J Agric Food Chem 56:8897-904. 2008....
Alkynylation of aryl halides with perfluoro-tagged palladium nanoparticles immobilized on silica gel under aerobic, copper- and phosphine-free conditions in waterRoberta Bernini
Dipartimento A B A C, Universita della Tuscia e Consorzio Universitario La Chimica per l Ambiente, Via S Camillo de Lellis, 01100 Viterbo, Italy
Org Biomol Chem 7:2270-3. 2009....
2-Arylhydroxytyrosol derivatives via Suzuki-Miyaura cross-couplingRoberta Bernini
Dipartimento A B A C, Universita degli Studi della Tuscia, Via S Camillo de Lellis, 01100 Viterbo, Italy
Org Lett 10:3457-60. 2008..A remarkable halide effect has been observed. 2-Iodo- and 2-bromohydroxytyrosol derivatives have been found to be ineffective cross-coupling partners in many cases. The acetonide and carbonate protecting groups can be readily removed...
