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DataTítuloAutor(es)TipoAcesso
2011Chemoenzymatic synthesis of 1-azafagomine analoguesMendes, Raquel; Duarte, Vera C. M.; Fortes, A. Gil, et al.Resumo em ata de conferência Acesso aberto
15-Jun-2022Concise synthesis of (S)-7-Hydroxy-5-aza-8a- epi - D -swainsonine from a d -erythrose derivativeSousa, Cristina E.A.; Salgueiro, Daniela A.L.; Alves, Maria José ChãoArtigoAcesso restrito UMinho
2011A concise synthesis of 8a-epi-swaisonine analogueAlves, M. José; Duarte, Vera C. M.; Fortes, A. Gil, et al.Resumo em ata de conferência Acesso aberto
16-Mar-2022Correction: Silva et al. Chemical profile and bioactivities of extracts from edible plants readily available in Portugal. Foods 2021, 10, 673Silva, Beatriz Nunes; Cadavez, Vasco; Santos, Pedro Miguel Ferreira, et al.CorrigendaAcesso aberto
2003Cycloaddition of methyl 2-(2,6-dichorophenyl)-2H-azirine-3-carboxylate to electron rich 2-azadienesAlves, M. José; Durães, M. Miguel; Fortes, A. GilArtigoAcesso aberto
Abr-2016Development of nanoparticles for antimicrobial protection of leather coatingsPinheiro, Inês; Alves, Maria José Chão; Coutinho, Paulo J. G., et al.Resumo em ata de conferência Acesso restrito UMinho
2012Diastereo-selectivity in diels–alder cycloadditions of erythrose benzylidene-acetal 1,3-Butadienes with maleimidesSalgueiro, D. A. L.; Duarte, Vera C. M.; Sousa, Cristina, et al.ArtigoAcesso aberto
2012Diastereo-selectivity of diels-alder cycloaddtions of erythrose benzylidene-acetal 1,3-Butadienes with maleimidesSalgueiro, D. A. L.; Duarte, Vera C. M.; Alves, M. José, et al.Resumo em ata de conferência Acesso aberto
2015Diastereoselective synthesis of analogues of neuraminic acidDuarte, Vera C. M.; Fortes, A. Gil; Alves, Maria José ChãoComunicação em painel Acesso aberto
2012Diels-alder cycloaddition in the synthesis of 1-azafagomine, analogs, and derivatives as glycosidase inhibitorsSalgueiro, D. A. L.; Sousa, Cristina; Fortes, A. Gil, et al.ArtigoAcesso aberto
2004Diels-alder cycloaddition of 2-azadienes to methyl 2-(2,6-dichlorophenyl)-2H-azirine-3-carboxylate in the synthesis of methyl 4-oxo-1,3-diazabicyclo[4.1.0]heptane-6-carboxylatesAlves, M. José; Durães, M. Miguel; Fortes, A. GilArtigoAcesso aberto
2001Diels–alder reactions of alkyl 2H-azirine-3-carboxylates with furansAlves, M. José; Azóia, Nuno G.; Bickley, Jamie F., et al.ArtigoAcesso aberto
1-Jul-2014Enantioselective diels-alder cycloadditions in the synthesis of two enantiomeric sets of chiral polyhydroxylated pipecolic acid derivativesDuarte, Vera C. M.; Alves, Maria José Chão; Fortes, A. GilArtigoAcesso restrito autor
2011Enantioselective Diels-Alder methodology in the synthesis of azasugarsDuarte, Vera C. M.; Fortes, A. Gil; Alves, M. JoséResumo em ata de conferência Acesso aberto
9-Jan-2013Enantiospecific 1,3-Dipolar Cycloadditions between Azadienophiles and 2-Phenyl-4,4a-dihydropyrano[3,2-d][1,3]dioxin-6(8aH)-oneRibeiro, Antonio; Alves, M. José; Sousa, Cristina, et al.Resumo em ata de conferência Acesso aberto
2005Ethyl 3-(2-pyridyl)-2H-azirine-2-carboxylate : synthesis and reactivity with dienesAlves, M. José; Fortes, A. Gil; Lemos, Américo, et al.ArtigoAcesso aberto
2015Evaluation of new naphthalimides as potential anticancer agents against breast cancer MCF-7, pancreatic cancer BxPC-3 and colon cancer HCT- 15 cell linesNoro, Jennifer Martins; Maciel, J.; Duarte, D., et al.ArtigoAcesso restrito autor
2016Exploiting the antiparasitic activity of naphthalimides derivativesSilva, Anabela Cordeiro da; Alves, Maria José Chão; Thoo-Lin, Paul Kong, et al.ArtigoAcesso aberto
2023Golgi α-mannosidase: opposing structures of Drosophila melanogaster and novel human model using molecular dynamics simulations and docking at different pHsDrogalin, Artem; Monteiro, Luís S.; Alves, Maria José Chão, et al.ArtigoAcesso aberto
2011Highly diastereoselective synthesis of 2-azabicyclo[2.2.1]hept-5-ene derivatives : bronsted acid catalized aza-diels-alder reaction between cyclopentadiene and imino-acetates with two chiral auxiliariesGarcía-Mera, Xerardo; Rodríguez-Borges, José E.; Vale, M. Luísa C., et al.ArtigoAcesso aberto
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