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Artigo de periodico
Synthesis of indole derivatives by domino hydroformylation/indolization of 2-nitrocinnamaldehydes (2008)
Marchetti, M.; Paganelli, S.; Carboni, D.; Ulgheri, F.; Del Ponte, Gino
Source: Journal of Molecular Catalysis A: Chemical. Unidade: FCFRP
Assunto: FÁRMACOS (SÍNTESE)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MARCHETTI, M. et al. Synthesis of indole derivatives by domino hydroformylation/indolization of 2-nitrocinnamaldehydes. Journal of Molecular Catalysis A: Chemical, v. 288, n. 1-2, p. 103-108, 2008Tradução . . Disponível em: https://doi.org/10.1016/j.molcata.2008.03.025. Acesso em: 18 nov. 2024.
APA
Marchetti, M., Paganelli, S., Carboni, D., Ulgheri, F., & Del Ponte, G. (2008). Synthesis of indole derivatives by domino hydroformylation/indolization of 2-nitrocinnamaldehydes. Journal of Molecular Catalysis A: Chemical, 288( 1-2), 103-108. doi:10.1016/j.molcata.2008.03.025
NLM
Marchetti M, Paganelli S, Carboni D, Ulgheri F, Del Ponte G. Synthesis of indole derivatives by domino hydroformylation/indolization of 2-nitrocinnamaldehydes [Internet]. Journal of Molecular Catalysis A: Chemical. 2008 ; 288( 1-2): 103-108.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.molcata.2008.03.025
Vancouver
Marchetti M, Paganelli S, Carboni D, Ulgheri F, Del Ponte G. Synthesis of indole derivatives by domino hydroformylation/indolization of 2-nitrocinnamaldehydes [Internet]. Journal of Molecular Catalysis A: Chemical. 2008 ; 288( 1-2): 103-108.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.molcata.2008.03.025
Artigo de periodico
Rational design of novel diketoacid-containing ferrocene inhibitors of HIV-1 integrase (2005)
Silva, Carlos H. T. P.; Del Ponte, Gino; Federman Neto, Alberto; Taft, Carlton A.
Source: Biooeganic Chemistry. Unidade: FCFRP
Assunto: FÁRMACOS (SÍNTESE)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Carlos H. T. P. et al. Rational design of novel diketoacid-containing ferrocene inhibitors of HIV-1 integrase. Biooeganic Chemistry, v. 33, p. 274-284, 2005Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2005.03.001. Acesso em: 18 nov. 2024.
APA
Silva, C. H. T. P., Del Ponte, G., Federman Neto, A., & Taft, C. A. (2005). Rational design of novel diketoacid-containing ferrocene inhibitors of HIV-1 integrase. Biooeganic Chemistry, 33, 274-284. doi:10.1016/j.bioorg.2005.03.001
NLM
Silva CHTP, Del Ponte G, Federman Neto A, Taft CA. Rational design of novel diketoacid-containing ferrocene inhibitors of HIV-1 integrase [Internet]. Biooeganic Chemistry. 2005 ; 33 274-284.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.bioorg.2005.03.001
Vancouver
Silva CHTP, Del Ponte G, Federman Neto A, Taft CA. Rational design of novel diketoacid-containing ferrocene inhibitors of HIV-1 integrase [Internet]. Biooeganic Chemistry. 2005 ; 33 274-284.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.bioorg.2005.03.001
Artigo de periodico
Asymmetric synthesis of 'gama'-butyrolactones by enantioselective hydrogenation of butenolides (2003)
Donate, Paulo Marcos; Frederico, Daniel; Silva, Rosangela da; Constantino, Maurício Gomes; Del Ponte, Gino; Bonatto, Pierina Sueli
Source: Tetrahedron. Unidades: FFCLRP, FCFRP
Assunto: FÁRMACOS (QUÍMICA)
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DONATE, Paulo Marcos et al. Asymmetric synthesis of 'gama'-butyrolactones by enantioselective hydrogenation of butenolides. Tetrahedron, v. 14, p. 3253-3256, 2003Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2003.08.031. Acesso em: 18 nov. 2024.
APA
Donate, P. M., Frederico, D., Silva, R. da, Constantino, M. G., Del Ponte, G., & Bonatto, P. S. (2003). Asymmetric synthesis of 'gama'-butyrolactones by enantioselective hydrogenation of butenolides. Tetrahedron, 14, 3253-3256. doi:10.1016/j.tetasy.2003.08.031
NLM
Donate PM, Frederico D, Silva R da, Constantino MG, Del Ponte G, Bonatto PS. Asymmetric synthesis of 'gama'-butyrolactones by enantioselective hydrogenation of butenolides [Internet]. Tetrahedron. 2003 ; 14 3253-3256.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.tetasy.2003.08.031
Vancouver
Donate PM, Frederico D, Silva R da, Constantino MG, Del Ponte G, Bonatto PS. Asymmetric synthesis of 'gama'-butyrolactones by enantioselective hydrogenation of butenolides [Internet]. Tetrahedron. 2003 ; 14 3253-3256.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/j.tetasy.2003.08.031
Artigo de periodico
Preparation of (Z)-1-(3-nitrophenyl)-4-phenylbut-1-ene and (Z)-1-(3-nitrophenyl)-5-phenylpent-1-ene by Pd(0)-catalyzed cross-coupling reaction (2003)
Del Ponte, Gino; Arcanjo, Fernando Costa; Botteghi, Carlo
Source: Journal of Molecular Catalysis A. Unidade: FCFRP
Subjects: QUÍMICA, FARMÁCIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
DEL PONTE, Gino e ARCANJO, Fernando Costa e BOTTEGHI, Carlo. Preparation of (Z)-1-(3-nitrophenyl)-4-phenylbut-1-ene and (Z)-1-(3-nitrophenyl)-5-phenylpent-1-ene by Pd(0)-catalyzed cross-coupling reaction. Journal of Molecular Catalysis A, v. 192, p. 35-40, 2003Tradução . . Disponível em: https://doi.org/10.1016/s1381-1169(02)00004-3. Acesso em: 18 nov. 2024.
APA
Del Ponte, G., Arcanjo, F. C., & Botteghi, C. (2003). Preparation of (Z)-1-(3-nitrophenyl)-4-phenylbut-1-ene and (Z)-1-(3-nitrophenyl)-5-phenylpent-1-ene by Pd(0)-catalyzed cross-coupling reaction. Journal of Molecular Catalysis A, 192, 35-40. doi:10.1016/s1381-1169(02)00004-3
NLM
Del Ponte G, Arcanjo FC, Botteghi C. Preparation of (Z)-1-(3-nitrophenyl)-4-phenylbut-1-ene and (Z)-1-(3-nitrophenyl)-5-phenylpent-1-ene by Pd(0)-catalyzed cross-coupling reaction [Internet]. Journal of Molecular Catalysis A. 2003 ; 192 35-40.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/s1381-1169(02)00004-3
Vancouver
Del Ponte G, Arcanjo FC, Botteghi C. Preparation of (Z)-1-(3-nitrophenyl)-4-phenylbut-1-ene and (Z)-1-(3-nitrophenyl)-5-phenylpent-1-ene by Pd(0)-catalyzed cross-coupling reaction [Internet]. Journal of Molecular Catalysis A. 2003 ; 192 35-40.[citado 2024 nov. 18 ] Available from: https://doi.org/10.1016/s1381-1169(02)00004-3
Artigo de periodico
New synthesis of ferrocene monocarboxylic acid and systematic studies on the preparation of related key-intermediates (2002)
Federman Neto, Alberto; Miller, Joseph; Andrade, Vânia Faria de; Fujimoto, Susana Yumi; Afonso, Márcia Maísa de Freitas; Archanjo, Fernando Costa; Darin, Vítor André; Silva, Márcio Luís Andrade e; Borges, Áurea Dinizete Lanchote; Del Ponte, Gino
Source: Zeitschrift fuer Anorganische und Allgemeine Chemie. Unidades: FCFRP, FFCLRP
Assunto: QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FEDERMAN NETO, Alberto et al. New synthesis of ferrocene monocarboxylic acid and systematic studies on the preparation of related key-intermediates. Zeitschrift fuer Anorganische und Allgemeine Chemie, v. 628, p. 209-216, 2002Tradução . . Acesso em: 18 nov. 2024.
APA
Federman Neto, A., Miller, J., Andrade, V. F. de, Fujimoto, S. Y., Afonso, M. M. de F., Archanjo, F. C., et al. (2002). New synthesis of ferrocene monocarboxylic acid and systematic studies on the preparation of related key-intermediates. Zeitschrift fuer Anorganische und Allgemeine Chemie, 628, 209-216.
NLM
Federman Neto A, Miller J, Andrade VF de, Fujimoto SY, Afonso MM de F, Archanjo FC, Darin VA, Silva MLA e, Borges ÁDL, Del Ponte G. New synthesis of ferrocene monocarboxylic acid and systematic studies on the preparation of related key-intermediates. Zeitschrift fuer Anorganische und Allgemeine Chemie. 2002 ; 628 209-216.[citado 2024 nov. 18 ]
Vancouver
Federman Neto A, Miller J, Andrade VF de, Fujimoto SY, Afonso MM de F, Archanjo FC, Darin VA, Silva MLA e, Borges ÁDL, Del Ponte G. New synthesis of ferrocene monocarboxylic acid and systematic studies on the preparation of related key-intermediates. Zeitschrift fuer Anorganische und Allgemeine Chemie. 2002 ; 628 209-216.[citado 2024 nov. 18 ]

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