Zobrazeno 1 - 10
of 15
pro vyhledávání: '"M. Fernanda Proença"'
Autor:
Filipe Areias, Carla Correia, Ashly Rocha, Sofia Teixeira, Marián Castro, Jose Brea, Huabin Hu, Jens Carlsson, Maria I. Loza, M. Fernanda Proença, M. Alice Carvalho
Publikováno v:
Molecules, Vol 29, Iss 11, p 2543 (2024)
A set of 2-aryl-9-H or methyl-6-morpholinopurine derivatives were synthesized and assayed through radioligand binding tests at human A1, A2A, A2B, and A3 adenosine receptor subtypes. Eleven purines showed potent antagonism at A1, A3, dual A1/A2A, A1/
Externí odkaz:
https://doaj.org/article/7cbea8944ba641e096dee5b96a2e909e
Autor:
Mariana M. Silva, Daniel Ribeiro, Eunice Cunha, M. Fernanda Proença, Robert J. Young, Maria C. Paiva
Publikováno v:
Nanomaterials, Vol 9, Iss 10, p 1416 (2019)
Single walled carbon nanotubes (SWCNT) were functionalized using the 1,3-dipolar cycloaddition reaction of an azomethine ylide under solvent-free conditions, a one-pot procedure that yields pyrrolidine type of groups at the nanotubes surface. The fun
Externí odkaz:
https://doaj.org/article/b171e42cbb2d4d6483181afc90b1b2b8
Autor:
Ana Bettencourt, Marián Castro, João Silva, Francisco Fernandes, Olga Coutinho, M. João Sousa, M. Fernanda Proença, Filipe Areias
Publikováno v:
Molecules, Vol 23, Iss 10, p 2530 (2018)
A selection of 1-amino-2-arylidenamine-1,2-(dicyano)ethenes 3 was synthesized and cyclized to 2-aryl-4,5-dicyano-1H-imidazoles 4 upon reflux in ethyl acetate/acetonitrile, in the presence of manganese dioxide. These compounds were tested for their an
Externí odkaz:
https://doaj.org/article/d0542d8b37f5466c8bad75f0c23d48b7
Autor:
Tânia Peixoto, Joana Nunes, Maria A. Lopes, Elina Marinho, M. Fernanda Proença, Paulo E. Lopes, Maria C. Paiva
Publikováno v:
Polymer Composites. 43:8409-8425
Autor:
Fábio, Pedroso de Lima, Emilio, Lence, Pilar, Suárez de Cepeda, Carla, Correia, M Alice, Carvalho, Concepción, González-Bello, M Fernanda, Proença
Publikováno v:
ACS omega. 7(27)
The reactivity of the diaminomaleonitrile-based imines containing hydroxyphenyl substituents with diverse aromatic aldehydes has been explored for the synthesis of novel highly substituted nitrogen heterocycles, which are considered privileged scaffo
Autor:
Fábio Pedroso de Lima, Emilio Lence, Pilar Suárez de Cepeda, Carla Correia, M. Alice Carvalho, Concepción González-Bello, M. Fernanda Proença
The reactivity of the diaminomaleonitrile-based imines containing hydroxyphenyl substituents with diverse aromatic aldehydes has been explored for the synthesis of novel highly substituted nitrogen heterocycles, which are considered privileged scaffo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b12bdd14b8af2261e717f39e61999115
https://hdl.handle.net/1822/81239
https://hdl.handle.net/1822/81239
Autor:
Filipe, Areias, Carla, Correia, Ashly, Rocha, José, Brea, Marián, Castro, Maria I, Loza, M Fernanda, Proença, M Alice, Carvalho
Publikováno v:
Bioorganicmedicinal chemistry. 27(16)
From a collection containing more than 1500 academic compounds, in silico screening identified a hit for the human A
Autor:
Marta Costa, M. Fernanda Proença
Publikováno v:
Comprehensive Organic Chemistry Experiments for the Laboratory Classroom ISBN: 9781849739634
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::18e6d2ccd206fdb418f0d6f892269874
https://doi.org/10.1039/9781849739634-00387
https://doi.org/10.1039/9781849739634-00387
Autor:
F. Taveira Pinto, M. Fernanda Proença, Rodrigo Maia, J. Pedro Pêgo, Maria Manuela Lima, Ana Cristina Neves, Elsa Carvalho
O desenvolvimento da anemometria laser Doppler (LDA-Laser Doppler Anemometry) teve um impacto significativo na investigação nas áreas da Mecânica dos Fluidos e da Hidráulica, obtendo desde o início de um bom acolhimento por parte da comunidade
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1406::e204319a7b01fa5ffa4bfb1781ea1317
https://hdl.handle.net/10216/93664
https://hdl.handle.net/10216/93664
Publikováno v:
The Journal of organic chemistry. 66(25)
A reinvestigation of the reactions of urea derivatives of diaminomaleonitrile 2 with aldehydes or ketones in the presence of triethylamine has established that the products of these reactions are not pyrimidino[5,4-d]pyrimidines 9 as previously repor