Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Mário A. Marangoni"'
Autor:
Helio G. Bonacorso, Marcos A. P. Martins, Sara Marchesan Oliveira, Nilo Zanatta, Evelyne da Silva Brum, Indiara Brusco, Mário A. Marangoni, Paulo A. Moraes, Pablo A. Nogara, João Rocha, Adriano F. Camargo, Marcio M. Lobo
Publikováno v:
ChemistrySelect. 5:14620-14625
Autor:
Marcos A. P. Martins, João Rocha, Helio G. Bonacorso, Adriano F. Camargo, Carlos E. Bencke, Mário A. Marangoni, Pablo A. Nogara, Paulo A. Moraes, Nilo Zanatta, Blessing A. Afolabi
Publikováno v:
Synthesis. 52:2347-2356
The regioselective synthesis of twenty novel [3-substituted 5-hydroxy-5-(trifluoromethyl)-4,5-dihydro-1H-pyrazol-1-yl][6-aryl-(2-methylthio)pyrimidin-4-yl]methanones from the cyclocondensation reactions of new 6-aryl-2-(methylthio)pyrimidine-4-carboh
Autor:
Marcos A. P. Martins, Paulo A. Moraes, Helio G. Bonacorso, Adriano F. Camargo, Mário A. Marangoni, Nilo Zanatta
Publikováno v:
Synthesis. 52:2528-2534
The 1,4-dicarbonyl scaffold ethyl 3-formyl-4,5-dihydrofuran-2-carboxylate was obtained through the rearrangement of the parent ethyl 2-(4,5-dihydrofuran-3-yl)-2-oxoacetate and applied to the synthesis of a series of 7-alkoxy-2,3-dihydrofuro[2,3-d]pyr
Autor:
Paulo A. Moraes, Clarissa P. Frizzo, Nilo Zanatta, Mário A. Marangoni, Marcos A. P. Martins, Alexandre R. Meyer, Marcio M. Lobo, Helio G. Bonacorso
Publikováno v:
Organic & Biomolecular Chemistry. 17:2384-2392
Reaction of 5-bromo enones with pyrazoles provided a series of unexpected N,O-aminal derivatives, through a 1,4-conjugated addition at the β-carbon of the 5-bromo enones instead of the expected nucleophilic substitution of the bromine. This reaction
Publikováno v:
Tetrahedron Letters. 58:4057-4061
A new, simple, and efficient method for the synthesis a novel series of 1-substituted 4-(trifluoromethyl)-5-(alkan-1-ol)-pyridin-2(1 H )-imines from the reaction of 3-(5,6-dihydro-4 H -pyran-3-yl)-4,4,4-trifluorobut-2-enenitrile and 3-(4,5-dihydrofur
Autor:
Helio G. Bonacorso, Adriano F. Camargo, Mário A. Marangoni, Carlos E. Bencke, Cassio A. Fantinel, Nilo Zanatta, Marcos A. P. Martins
Publikováno v:
Synthesis. 49:5131-5142
Three new series of compounds, 5-alkoxy-3-(trifluoromethyl)penta-2,4-dienenitriles, 5-(phenylthio)-3-(trifluoromethyl)penta-2,4-dienenitriles, and ethyl 4-alkoxy-2-(cyanomethylene)but-3-enoates, obtained from the olefination reaction of the respectiv
Autor:
Cassio A. Fantinel, Carlos E. Bencke, Adriano F. Camargo, Mário A. Marangoni, Andressa S. Fortes, Marcos A. P. Martins, Helio G. Bonacorso, Nilo Zanatta
Publikováno v:
Synthesis. 47:827-835
A simple and efficient procedure for the synthesis of ethyl 2-methylthio- and ethyl 2-benzylthio-6-methyl(aryl)-pyrimidine-4-carboxylates and their corresponding acid derivatives is reported. The products are obtained in good yields via the cyclocond
Autor:
Cassio A. Fantinel, Andressa S. Fortes, Adriano F. Camargo, Helio G. Bonacorso, Mário A. Marangoni, Carlos E. Bencke, Nilo Zanatta, Marcos A. P. Martins
Publikováno v:
ChemInform. 46
The simple preparation of the title compounds succeeds in moderate to good yields via cyclocondensation of 4-substituted ethyl 4-alkoxy-2-oxobut-3-eneoates with 2-methyl or 2-benzylisothiourea.
Autor:
Cassio A. Fantinel, Carlos E. Bencke, Helio G. Bonacorso, Nilo Zanatta, Mário A. Marangoni, Andressa S. Fortes, Marcos A. P. Martins
Publikováno v:
Proceedings of the 14th Brazilian Meeting on Organic Synthesis Proceedings.
Many trifluoromethylated heterocycles showing remarkable biological activity have been widely used in a variety of fields ranging from medicine to agricultural products, besides of being versatile intermediate for the synthesis of biologically active