Mário Calvete

Dr. Mário Calvete

orcid

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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10 November 2016 in Chemical Reviews
Verified
Journal Article
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DDDanilo Dini
Danilo Dini
Mário CalveteMário Calvete
Mário Calvete
MHMichael Hanack
Michael Hanack

1 March 2004 in Synthetic Metals
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Journal Article
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Mário CalveteMário Calvete
Mário Calvete
GYGuo Ying Yang
Guo Ying Yang
MHMichael Hanack
Michael Hanack

10 October 2018 in ACS Catalysis
Verified
Journal Article
Closed access
Mariette PereiraMariette Pereira
Mariette Pereira
LDLucas Dias
Lucas Dias
Mário CalveteMário Calvete
Mário Calvete

19 June 2013 in Chemical Society Reviews
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Journal Article
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PDF file
Mariette PereiraMariette Pereira
Mariette Pereira
Mário CalveteMário Calvete
Mário Calvete
Rui CarrilhoRui Carrilho
Rui Carrilho
AAArtur R. Abreu
Artur R. Abreu
The development of large scale synthesis of enantiopure and thermally stable (R)- and (S)-BINOL molecules constitutes a key milestone in the field of asymmetric catalysis. Particularly, a great variety of chiral binaphthyl-based phosphorus compounds, herein represented by phosphite and phosphine classes, have earned considerable relevance due to their versatility as ligands in enantioselective metal-catalysed reactions, allowing the preparation of optically active products with the desired enantiopurity. This review highlights the most relevant concepts and accounts regarding general synthetic procedures for binaphthyl-based mono- and bidentate phosphites and phosphines. Furthermore, the search for environmentally benign chemical catalytic processes compelled us to also give special attention to the functionalisation of binaphthyl-based phosphorus ligands for use in alternative reaction media. When available, a critical selection of their applications in catalysis is briefly assessed.

14 February 2020 in Photochemical & Photobiological Sciences
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Journal Article
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NMNidia Maldonado-Carmona
Nidia Maldonado-Carmona
TOTan-Sothea Ouk
Tan-Sothea Ouk
Mário CalveteMário Calvete
Mário Calvete
Mariette PereiraMariette Pereira
Mariette Pereira
NVNicolas Villandier
Nicolas Villandier
Stéphanie LhezStéphanie Lhez
Stéphanie Lhez
Antimicrobial resistance is threatening to overshadow last century's medical advances. Previously eradicated infectious diseases are now resurgent as multi-drug resistant strains, leading to expensive, toxic and, in some cases, ineffective antimicrobial treatments. Given this outlook, researchers are willing to investigate novel antimicrobial treatments that may be able to deal with antimicrobial resistance, namely photodynamic therapy (PDT). PDT relies on the generation of toxic reactive oxygen species (ROS) in the presence of light and a photosensitizer (PS) molecule. PDT has been known for almost a century, but most of its applications have been directed towards the treatment of cancer and topical diseases. Unlike classical antimicrobial chemotherapy treatments, photodynamic antimicrobial chemotherapy (PACT) has a non-target specific mechanism of action, based on the generation of ROS, working against cellular membranes, walls, proteins, lipids and nucleic acids. This non-specific mechanism diminishes the chances of bacteria developing resistance. However, PSs usually are large molecules, prone to aggregation, diminishing their efficiency. This review will report the development of materials obtained from natural sources, as delivery systems for photosensitizing molecules against microorganisms. The present work emphasizes on the biological results rather than on the synthesis routes to prepare the conjugates. Also, it discusses the current state of the art, providing our perspective on the field.

18 September 2012 in European Journal of Organic Chemistry
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Journal Article
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ÂNÂngela C. B. Neves
Ângela C. B. Neves
Mário CalveteMário Calvete
Mário Calvete
Teresa  Pinho E MeloTeresa Pinho E Melo
Teresa Pinho E Melo
Mariette PereiraMariette Pereira
Mariette Pereira