A
Artur M. S. Silva
Researcher at University of Aveiro
Publications - 961
Citations - 19708
Artur M. S. Silva is an academic researcher from University of Aveiro. The author has contributed to research in topics: Catalysis & Chemistry. The author has an hindex of 54, co-authored 895 publications receiving 15627 citations. Previous affiliations of Artur M. S. Silva include University of Porto & University of Santiago de Compostela.
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Evolution of Acridines and Xanthenes as a Core Structure for the Development of Antileishmanial Agents
TL;DR: In this review, a thorough compilation of the most promising antileishmanial acridine and xanthene derivatives is performed from both natural and synthetic origins to highlight the relevance of nitrogen- and oxygen-containing tricyclic heterocycles, particularly acridines and xanine derivatives, for the development of treatments against leishmaniasis.
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Synthesis of Novel 3-Alkyl-3′,4′,5,7-Tetrahydroxyflavones
TL;DR: The 3-alkyl-3-4-5,7-tetramethoxyflavones were demethylated with boron tribromide.
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Synthesis of Benzophenones and in vitro Evaluation of Their Anticancer Potential in Breast and Prostate Cancer Cells
Lydia Saidi,Djenisa H. A. Rocha,Oualid Talhi,Yamina Bentarzi,Bellara Nedjar-Kolli,Khaldoun Bachari,Filipe A. Almeida Paz,Luisa A. Helguero,Artur M. S. Silva +8 more
TL;DR: The synthesis of substituted 2‐hydroxybenzophenones through 1,4‐conjugate addition/intramolecular cycloaddition/dehydration of nitromethane on key intermediate chromones is reported, which exhibited good cytotoxic effects against the three cancer cell lines.
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Constituents of Polyalthia jucunda. and Their Cytotoxic Effect on Human Cancer Cell Lines
Areerat Suedee,Ing-On Mondranondra,Anake Kijjoa,Madalena Pinto,Nair Nazareth,Maria São José Nascimento,Artur M. S. Silva,Werner Herz +7 more
TL;DR: In this article, Piere et al. isolated four compounds from the stem bark of Polyalthia jucunda, including 4-hydroxy-4, 7-dimethyl-α.-tetralone (1), 4,5-dihydroblumenol A (2), N.-trans-feruloyltyramine (3), and 24-methylenelanosta-7, 9(11)-dien-3-β., 15α.-diol (4) were evaluated for their effects on growth.
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Reactivity of 3-Iodo-4-quinolonesin Heck Reactions: Synthesis of Novel (E)-3-Styryl-4-quinolones
TL;DR: In this paper, a new and efficient route for the synthesis of (E)-N-methyl-3-styryl-4-quinolones is described, which involves the Heck reaction of N-methyl, 3-iodo-4 -quinolone, which is obtained by consecutive 3iodination and NH-methylation of the unsubstituted 4-quinoline with styrene derivatives.