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Artigo de periodico
Copper-catalyzed NeH insertion reactions from sulfoxonium ylides (2020)
Furniel, Lucas Giani; Burtoloso, Antonio Carlos Bender
Source: Tetrahedron. Unidade: IQSC
Subjects: CATÁLISE, COBRE
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ABNT
FURNIEL, Lucas Giani e BURTOLOSO, Antonio Carlos Bender. Copper-catalyzed NeH insertion reactions from sulfoxonium ylides. Tetrahedron, v. 76, n. 51, p. 131313, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2020.131313. Acesso em: 13 jun. 2025.
APA
Furniel, L. G., & Burtoloso, A. C. B. (2020). Copper-catalyzed NeH insertion reactions from sulfoxonium ylides. Tetrahedron, 76( 51), 131313. doi:10.1016/j.tet.2020.131313
NLM
Furniel LG, Burtoloso ACB. Copper-catalyzed NeH insertion reactions from sulfoxonium ylides [Internet]. Tetrahedron. 2020 ; 76( 51): 131313.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2020.131313
Vancouver
Furniel LG, Burtoloso ACB. Copper-catalyzed NeH insertion reactions from sulfoxonium ylides [Internet]. Tetrahedron. 2020 ; 76( 51): 131313.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2020.131313
Artigo de periodico
Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry (2020)
Perecim, Givago P.; Deflon, Victor Marcelo ; Martins, Gabriel R.; Pinto, Leandro M.C.; Casagrande, Gleison Antônio ; Silva, Diogo Oliveira; Raminelli, Cristiano
Source: Tetrahedron. Unidade: IQSC
Subjects: ALCALOIDES, QUÍMICA
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ABNT
PERECIM, Givago P. et al. Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry. Tetrahedron, v. 76. 131461 July 2020, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2020.131461. Acesso em: 13 jun. 2025.
APA
Perecim, G. P., Deflon, V. M., Martins, G. R., Pinto, L. M. C., Casagrande, G. A., Silva, D. O., & Raminelli, C. (2020). Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry. Tetrahedron, 76. 131461 July 2020. doi:10.1016/j.tet.2020.131461
NLM
Perecim GP, Deflon VM, Martins GR, Pinto LMC, Casagrande GA, Silva DO, Raminelli C. Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry [Internet]. Tetrahedron. 2020 ; 76. 131461 July 2020[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2020.131461
Vancouver
Perecim GP, Deflon VM, Martins GR, Pinto LMC, Casagrande GA, Silva DO, Raminelli C. Stereoselective total synthesis of (S)- and (R)-nuciferine using benzyne chemistry [Internet]. Tetrahedron. 2020 ; 76. 131461 July 2020[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2020.131461
Artigo de periodico
Recent applications of magnesium- and Zinc-TMP amides in the synthesis of bioactive targets (2019)
Nishimura, Rodolfo Hideki Vicente ; Vaz, Artur de Lara Lima ; Bozzini, Leandro Alves ; Murie, Valter Eduardo ; Clososki, Giuliano Cesar
Source: Tetrahedron. Unidades: FCFRP, FFCLRP
Subjects: AMIDO, MAGNÉSIO, ZINCO, SÍNTESE QUÍMICA, FÁRMACOS, PRODUTOS NATURAIS
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ABNT
NISHIMURA, Rodolfo Hideki Vicente et al. Recent applications of magnesium- and Zinc-TMP amides in the synthesis of bioactive targets. Tetrahedron, v. 75, n. 4, p. 464-474, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2018.12.018. Acesso em: 13 jun. 2025.
APA
Nishimura, R. H. V., Vaz, A. de L. L., Bozzini, L. A., Murie, V. E., & Clososki, G. C. (2019). Recent applications of magnesium- and Zinc-TMP amides in the synthesis of bioactive targets. Tetrahedron, 75( 4), 464-474. doi:10.1016/j.tet.2018.12.018
NLM
Nishimura RHV, Vaz A de LL, Bozzini LA, Murie VE, Clososki GC. Recent applications of magnesium- and Zinc-TMP amides in the synthesis of bioactive targets [Internet]. Tetrahedron. 2019 ; 75( 4): 464-474.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2018.12.018
Vancouver
Nishimura RHV, Vaz A de LL, Bozzini LA, Murie VE, Clososki GC. Recent applications of magnesium- and Zinc-TMP amides in the synthesis of bioactive targets [Internet]. Tetrahedron. 2019 ; 75( 4): 464-474.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2018.12.018
Artigo de periodico
Synthesis of symmetrical biaryl compounds by homocoupling reaction (2019)
Vasconcelos, Stanley N. S; Reis, Joel S; Oliveira, Isadora M. de; Balfour, Michael N; Stefani, Hélio Alexandre
Source: Tetrahedron. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
VASCONCELOS, Stanley N. S et al. Synthesis of symmetrical biaryl compounds by homocoupling reaction. Tetrahedron, v. 75, p. 1865-1959, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2019.02.001. Acesso em: 13 jun. 2025.
APA
Vasconcelos, S. N. S., Reis, J. S., Oliveira, I. M. de, Balfour, M. N., & Stefani, H. A. (2019). Synthesis of symmetrical biaryl compounds by homocoupling reaction. Tetrahedron, 75, 1865-1959. doi:10.1016/j.tet.2019.02.001
NLM
Vasconcelos SNS, Reis JS, Oliveira IM de, Balfour MN, Stefani HA. Synthesis of symmetrical biaryl compounds by homocoupling reaction [Internet]. Tetrahedron. 2019 ; 75 1865-1959.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2019.02.001
Vancouver
Vasconcelos SNS, Reis JS, Oliveira IM de, Balfour MN, Stefani HA. Synthesis of symmetrical biaryl compounds by homocoupling reaction [Internet]. Tetrahedron. 2019 ; 75 1865-1959.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2019.02.001
Artigo de periodico
Organocatalytic asymmetric vinylogous 1,4-addition of a,a- Dicyanoolefins to chalcones under a bio-based reaction media: discovery of new Michael adducts with antiplasmodial activity (2019)
Martelli, Lorena S. R.; Vieira, Lucas C. C.; Paixão, Márcio W.; Zukerman-Schpector, Julio; Souza, Juliana O.; Aguiar, Anna Caroline C.; Oliva, Glaucius ; Guido, Rafael Victorio Carvalho ; Corrêa, Arlene G.
Source: Tetrahedron. Unidade: IFSC
Subjects: BIOQUÍMICA, PLASMODIUM FALCIPARUM, PLANEJAMENTO DE FÁRMACOS
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ABNT
MARTELLI, Lorena S. R. et al. Organocatalytic asymmetric vinylogous 1,4-addition of a,a- Dicyanoolefins to chalcones under a bio-based reaction media: discovery of new Michael adducts with antiplasmodial activity. Tetrahedron, v. 75, n. 25, p. 3530-3542, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2019.05.022. Acesso em: 13 jun. 2025.
APA
Martelli, L. S. R., Vieira, L. C. C., Paixão, M. W., Zukerman-Schpector, J., Souza, J. O., Aguiar, A. C. C., et al. (2019). Organocatalytic asymmetric vinylogous 1,4-addition of a,a- Dicyanoolefins to chalcones under a bio-based reaction media: discovery of new Michael adducts with antiplasmodial activity. Tetrahedron, 75( 25), 3530-3542. doi:10.1016/j.tet.2019.05.022
NLM
Martelli LSR, Vieira LCC, Paixão MW, Zukerman-Schpector J, Souza JO, Aguiar ACC, Oliva G, Guido RVC, Corrêa AG. Organocatalytic asymmetric vinylogous 1,4-addition of a,a- Dicyanoolefins to chalcones under a bio-based reaction media: discovery of new Michael adducts with antiplasmodial activity [Internet]. Tetrahedron. 2019 ; 75( 25): 3530-3542.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2019.05.022
Vancouver
Martelli LSR, Vieira LCC, Paixão MW, Zukerman-Schpector J, Souza JO, Aguiar ACC, Oliva G, Guido RVC, Corrêa AG. Organocatalytic asymmetric vinylogous 1,4-addition of a,a- Dicyanoolefins to chalcones under a bio-based reaction media: discovery of new Michael adducts with antiplasmodial activity [Internet]. Tetrahedron. 2019 ; 75( 25): 3530-3542.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2019.05.022
Artigo de periodico
Oxazoline as acceptor moiety for excited-state intramolecular proton transfer (2018)
Reis, Joel S; Fernandes, Arthur Bonfá; Dörr, Barbara Coelho de Freitas; Bastos, Erick Leite ; Stefani, Hélio Alexandre
Source: Tetrahedron. Unidades: IQ, FCF
Subjects: FLUORESCÊNCIA, COMPOSTOS ORGÂNICOS
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ABNT
REIS, Joel S et al. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer. Tetrahedron, v. 74, p. 6866-6872, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2018.10.019. Acesso em: 13 jun. 2025.
APA
Reis, J. S., Fernandes, A. B., Dörr, B. C. de F., Bastos, E. L., & Stefani, H. A. (2018). Oxazoline as acceptor moiety for excited-state intramolecular proton transfer. Tetrahedron, 74, 6866-6872. doi:10.1016/j.tet.2018.10.019
NLM
Reis JS, Fernandes AB, Dörr BC de F, Bastos EL, Stefani HA. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer [Internet]. Tetrahedron. 2018 ; 74 6866-6872.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2018.10.019
Vancouver
Reis JS, Fernandes AB, Dörr BC de F, Bastos EL, Stefani HA. Oxazoline as acceptor moiety for excited-state intramolecular proton transfer [Internet]. Tetrahedron. 2018 ; 74 6866-6872.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2018.10.019
Artigo de periodico
One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin (2017)
Dias, Rafael Mafra de Paula; Momo, Patrícia Betoni; Burtoloso, Antonio Carlos Bender
Source: Tetrahedron. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
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ABNT
DIAS, Rafael Mafra de Paula e MOMO, Patrícia Betoni e BURTOLOSO, Antonio Carlos Bender. One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin. Tetrahedron, v. 73, n. 26, p. 3720 - 3729, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2017.05.040. Acesso em: 13 jun. 2025.
APA
Dias, R. M. de P., Momo, P. B., & Burtoloso, A. C. B. (2017). One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin. Tetrahedron, 73( 26), 3720 - 3729. doi:10.1016/j.tet.2017.05.040
NLM
Dias RM de P, Momo PB, Burtoloso ACB. One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin [Internet]. Tetrahedron. 2017 ; 73( 26): 3720 - 3729.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2017.05.040
Vancouver
Dias RM de P, Momo PB, Burtoloso ACB. One-step syntheses of substituted 2-pyrrolidinones and 3- pyrrolidinones from a,b-unsaturated diazoketones and amines: Application in the synthesis of barmumycin [Internet]. Tetrahedron. 2017 ; 73( 26): 3720 - 3729.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2017.05.040
Artigo de periodico
Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol (2017)
Lima, Rafaely Nascimento; Porto, Andre Luiz Meleiro
Source: Tetrahedron. Unidade: IQSC
Assunto: QUÍMICA VERDE
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ABNT
LIMA, Rafaely Nascimento e PORTO, Andre Luiz Meleiro. Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol. Tetrahedron, v. 58, n. 9, p. 825-828, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2016.12.062. Acesso em: 13 jun. 2025.
APA
Lima, R. N., & Porto, A. L. M. (2017). Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol. Tetrahedron, 58( 9), 825-828. doi:10.1016/j.tetlet.2016.12.062
NLM
Lima RN, Porto ALM. Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol [Internet]. Tetrahedron. 2017 ; 58( 9): 825-828.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tetlet.2016.12.062
Vancouver
Lima RN, Porto ALM. Facile synthesis of new quinoxalines from ethyl gallate by green chemistry protocol [Internet]. Tetrahedron. 2017 ; 58( 9): 825-828.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tetlet.2016.12.062
Artigo de periodico
Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186 (2016)
Jimenez, David Esteban Quintero; Ferreira , Irlon Maciel; Birolli, Willian Garcia; Fonseca, Luis P.; Porto, Andre Luiz Meleiro
Source: Tetrahedron. Unidade: IQSC
Subjects: FUNGOS, QUÍMICA ORGÂNICA
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ABNT
JIMENEZ, David Esteban Quintero et al. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186. Tetrahedron, v. 72, n. 46, p. 7317-7322, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2016.02.014. Acesso em: 13 jun. 2025.
APA
Jimenez, D. E. Q., Ferreira , I. M., Birolli, W. G., Fonseca, L. P., & Porto, A. L. M. (2016). Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186. Tetrahedron, 72( 46), 7317-7322. doi:10.1016/j.tet.2016.02.014
NLM
Jimenez DEQ, Ferreira IM, Birolli WG, Fonseca LP, Porto ALM. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186 [Internet]. Tetrahedron. 2016 ; 72( 46): 7317-7322.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2016.02.014
Vancouver
Jimenez DEQ, Ferreira IM, Birolli WG, Fonseca LP, Porto ALM. Synthesis and biocatalytic ene-reduction of Knoevenagel condensation compounds by the marine-derived fungus Penicillium citrinum CBMAI 1186 [Internet]. Tetrahedron. 2016 ; 72( 46): 7317-7322.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2016.02.014
Artigo de periodico
Photochemistry of the hemiketal form of anthocyanins and its potential role in plant protection from UV-B radiation (2015)
Costa, Damien; Galvão, Adelino M; Di Paolo, Roberto E; Freitas, Adilson Alves de; Lima, João Carlos; Quina, Frank Herbert ; Maçanita, Antonio L
Source: Tetrahedron. Unidade: IQ
Subjects: FOTOQUÍMICA, RADIAÇÃO ULTRAVIOLETA
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ABNT
COSTA, Damien et al. Photochemistry of the hemiketal form of anthocyanins and its potential role in plant protection from UV-B radiation. Tetrahedron, v. 71, n. 20, p. 3157-3162, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2014.06.092. Acesso em: 13 jun. 2025.
APA
Costa, D., Galvão, A. M., Di Paolo, R. E., Freitas, A. A. de, Lima, J. C., Quina, F. H., & Maçanita, A. L. (2015). Photochemistry of the hemiketal form of anthocyanins and its potential role in plant protection from UV-B radiation. Tetrahedron, 71( 20), 3157-3162. doi:10.1016/j.tet.2014.06.092
NLM
Costa D, Galvão AM, Di Paolo RE, Freitas AA de, Lima JC, Quina FH, Maçanita AL. Photochemistry of the hemiketal form of anthocyanins and its potential role in plant protection from UV-B radiation [Internet]. Tetrahedron. 2015 ; 71( 20): 3157-3162.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2014.06.092
Vancouver
Costa D, Galvão AM, Di Paolo RE, Freitas AA de, Lima JC, Quina FH, Maçanita AL. Photochemistry of the hemiketal form of anthocyanins and its potential role in plant protection from UV-B radiation [Internet]. Tetrahedron. 2015 ; 71( 20): 3157-3162.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2014.06.092
Artigo de periodico
Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion (2015)
Campo, Vanessa Leiria; Ivanova, Irina M.; Carvalho, Ivone; Lopes, Carla Duque; Carneiro, Zumira, A.; Saalbach, Gerhard; Schenkman, Sérgio; Silva, João Santana da; Nepogodiev, Sergey A.; Field, Robert A.
Source: Tetrahedron. Unidades: FCFRP, FMRP
Subjects: TRIPANOSSOMICIDAS, TRYPANOSOMA CRUZI, MACRÓFAGOS
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ABNT
CAMPO, Vanessa Leiria et al. Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion. Tetrahedron, v. 71, n. 39, p. 7344–7353, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2015.04.085. Acesso em: 13 jun. 2025.
APA
Campo, V. L., Ivanova, I. M., Carvalho, I., Lopes, C. D., Carneiro, Z., Saalbach, G., et al. (2015). Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion. Tetrahedron, 71( 39), 7344–7353. doi:10.1016/j.tet.2015.04.085
NLM
Campo VL, Ivanova IM, Carvalho I, Lopes CD, Carneiro Z, Saalbach G, Schenkman S, Silva JS da, Nepogodiev SA, Field RA. Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion [Internet]. Tetrahedron. 2015 ; 71( 39): 7344–7353.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2015.04.085
Vancouver
Campo VL, Ivanova IM, Carvalho I, Lopes CD, Carneiro Z, Saalbach G, Schenkman S, Silva JS da, Nepogodiev SA, Field RA. Click chemistry oligomerisation of azido-alkyne-functionalised galactose accesses triazole-linked linear oligomers and macrocycles that inhibit Trypanosoma cruzi macrophage invasion [Internet]. Tetrahedron. 2015 ; 71( 39): 7344–7353.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2015.04.085
Artigo de periodico
Riboflavin derivatives for enhanced photodynamic activity against Leishmania parasites (2015)
Silva, Alexandre Vieira; Lopez Sanchez, Almudena; Junqueira, Helena Couto; Rivas, Luis; Baptista, Maurício da Silva ; Orellana, Guillermo
Source: Tetrahedron. Unidade: IQ
Subjects: LEISHMANIA, TERAPIA FOTODINÂMICA
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ABNT
SILVA, Alexandre Vieira et al. Riboflavin derivatives for enhanced photodynamic activity against Leishmania parasites. Tetrahedron, v. 71, n. 3, p. 457-462, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2014.11.072. Acesso em: 13 jun. 2025.
APA
Silva, A. V., Lopez Sanchez, A., Junqueira, H. C., Rivas, L., Baptista, M. da S., & Orellana, G. (2015). Riboflavin derivatives for enhanced photodynamic activity against Leishmania parasites. Tetrahedron, 71( 3), 457-462. doi:10.1016/j.tet.2014.11.072
NLM
Silva AV, Lopez Sanchez A, Junqueira HC, Rivas L, Baptista M da S, Orellana G. Riboflavin derivatives for enhanced photodynamic activity against Leishmania parasites [Internet]. Tetrahedron. 2015 ; 71( 3): 457-462.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2014.11.072
Vancouver
Silva AV, Lopez Sanchez A, Junqueira HC, Rivas L, Baptista M da S, Orellana G. Riboflavin derivatives for enhanced photodynamic activity against Leishmania parasites [Internet]. Tetrahedron. 2015 ; 71( 3): 457-462.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2014.11.072
Artigo de periodico
Palladium on magnetite: magnetically recoverable catalyst for selective hydrogenation of acetylenic to olefinic compounds (2014)
Silva, Fernanda Parra da; Rossi, Liane Marcia
Source: Tetrahedron. Unidade: IQ
Subjects: PALÁDIO, HIDROGENAÇÃO
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ABNT
SILVA, Fernanda Parra da e ROSSI, Liane Marcia. Palladium on magnetite: magnetically recoverable catalyst for selective hydrogenation of acetylenic to olefinic compounds. Tetrahedron, v. 70, n. 20, p. 3314-3318, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2013.10.051. Acesso em: 13 jun. 2025.
APA
Silva, F. P. da, & Rossi, L. M. (2014). Palladium on magnetite: magnetically recoverable catalyst for selective hydrogenation of acetylenic to olefinic compounds. Tetrahedron, 70( 20), 3314-3318. doi:10.1016/j.tet.2013.10.051
NLM
Silva FP da, Rossi LM. Palladium on magnetite: magnetically recoverable catalyst for selective hydrogenation of acetylenic to olefinic compounds [Internet]. Tetrahedron. 2014 ; 70( 20): 3314-3318.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2013.10.051
Vancouver
Silva FP da, Rossi LM. Palladium on magnetite: magnetically recoverable catalyst for selective hydrogenation of acetylenic to olefinic compounds [Internet]. Tetrahedron. 2014 ; 70( 20): 3314-3318.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2013.10.051
Artigo de periodico
Solvent-free Diels-Alder reactions catalyzed by `FE´`CL IND. 3´ on Aerosil® silica (2014)
Donatoni, Maria C; Junior, Gilmar A. B; Oliveira, Kleber T. de; Ando, Rômulo Augusto ; Brocksom, Timothy John; Santos, Alcindo Aparecido dos
Source: Tetrahedron. Unidade: IQ
Subjects: CATALASE, SOLVENTE
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ABNT
DONATONI, Maria C et al. Solvent-free Diels-Alder reactions catalyzed by `FE´`CL IND. 3´ on Aerosil® silica. Tetrahedron, v. 70, n. 20, p. 3231-3238, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2014.02.017. Acesso em: 13 jun. 2025.
APA
Donatoni, M. C., Junior, G. A. B., Oliveira, K. T. de, Ando, R. A., Brocksom, T. J., & Santos, A. A. dos. (2014). Solvent-free Diels-Alder reactions catalyzed by `FE´`CL IND. 3´ on Aerosil® silica. Tetrahedron, 70( 20), 3231-3238. doi:10.1016/j.tet.2014.02.017
NLM
Donatoni MC, Junior GAB, Oliveira KT de, Ando RA, Brocksom TJ, Santos AA dos. Solvent-free Diels-Alder reactions catalyzed by `FE´`CL IND. 3´ on Aerosil® silica [Internet]. Tetrahedron. 2014 ; 70( 20): 3231-3238.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2014.02.017
Vancouver
Donatoni MC, Junior GAB, Oliveira KT de, Ando RA, Brocksom TJ, Santos AA dos. Solvent-free Diels-Alder reactions catalyzed by `FE´`CL IND. 3´ on Aerosil® silica [Internet]. Tetrahedron. 2014 ; 70( 20): 3231-3238.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2014.02.017
Artigo de periodico-divulgacao
Professor Alcindo A. dos Santos (Biography) (2014)
Santos, Alcindo Aparecido dos
Source: Tetrahedron. Unidade: IQ
Assunto: BIOGRAFIAS
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ABNT
SANTOS, Alcindo Aparecido dos. Professor Alcindo A. dos Santos (Biography). Tetrahedron. Oxford: Instituto de Química, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.tet.2014.03.077. Acesso em: 13 jun. 2025. , 2014
APA
Santos, A. A. dos. (2014). Professor Alcindo A. dos Santos (Biography). Tetrahedron. Oxford: Instituto de Química, Universidade de São Paulo. doi:10.1016/j.tet.2014.03.077
NLM
Santos AA dos. Professor Alcindo A. dos Santos (Biography) [Internet]. Tetrahedron. 2014 ; 70 3229.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2014.03.077
Vancouver
Santos AA dos. Professor Alcindo A. dos Santos (Biography) [Internet]. Tetrahedron. 2014 ; 70 3229.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2014.03.077
Artigo de periodico
A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal (2014)
Bernardim, Barbara; Burtoloso, Antonio Carlos Bender
Source: Tetrahedron. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERNARDIM, Barbara e BURTOLOSO, Antonio Carlos Bender. A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal. Tetrahedron, v. 70, p. 3291-3296, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2013.10.059. Acesso em: 13 jun. 2025.
APA
Bernardim, B., & Burtoloso, A. C. B. (2014). A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal. Tetrahedron, 70, 3291-3296. doi:10.1016/j.tet.2013.10.059
NLM
Bernardim B, Burtoloso ACB. A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal [Internet]. Tetrahedron. 2014 ; 70 3291-3296.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2013.10.059
Vancouver
Bernardim B, Burtoloso ACB. A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal [Internet]. Tetrahedron. 2014 ; 70 3291-3296.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2013.10.059
Artigo de periodico
Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters (2014)
Stefani, Hélio Alexandre ; Manarin, Flávia; Sousa, Ariane C.S; Souza, Frederico B; Ferraz, Witor Ribeiro
Source: Tetrahedron. Unidade: FCF
Subjects: ITÉRBIO, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters. Tetrahedron, v. 70, n. 20, p. 3243-3248, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2013.11.107. Acesso em: 13 jun. 2025.
APA
Stefani, H. A., Manarin, F., Sousa, A. C. S., Souza, F. B., & Ferraz, W. R. (2014). Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters. Tetrahedron, 70( 20), 3243-3248. doi:10.1016/j.tet.2013.11.107
NLM
Stefani HA, Manarin F, Sousa ACS, Souza FB, Ferraz WR. Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters [Internet]. Tetrahedron. 2014 ; 70( 20): 3243-3248.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2013.11.107
Vancouver
Stefani HA, Manarin F, Sousa ACS, Souza FB, Ferraz WR. Three-component reaction for the synthesis of diverse β-unsaturated α-amino esters [Internet]. Tetrahedron. 2014 ; 70( 20): 3243-3248.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2013.11.107
Artigo de periodico-divulgacao
Applied organic synthesis in action [Preface]: strategies and process development (2014)
Santos, Alcindo Aparecido dos
Source: Tetrahedron. Unidade: IQ
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SANTOS, Alcindo Aparecido dos. Applied organic synthesis in action [Preface]: strategies and process development. Tetrahedron. Oxford: Instituto de Química, Universidade de São Paulo. Disponível em: https://doi.org/10.1016/j.tet.2014.02.053. Acesso em: 13 jun. 2025. , 2014
APA
Santos, A. A. dos. (2014). Applied organic synthesis in action [Preface]: strategies and process development. Tetrahedron. Oxford: Instituto de Química, Universidade de São Paulo. doi:10.1016/j.tet.2014.02.053
NLM
Santos AA dos. Applied organic synthesis in action [Preface]: strategies and process development [Internet]. Tetrahedron. 2014 ; 70 3230.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2014.02.053
Vancouver
Santos AA dos. Applied organic synthesis in action [Preface]: strategies and process development [Internet]. Tetrahedron. 2014 ; 70 3230.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2014.02.053
Artigo de periodico
Chemoenzymatic approaches to obtain chiral-centered selenium compounds (2012)
Brondani, Patricia Bulegon; Guilmoto, Nathalie Mariana Andrade de França; Dudek, Hanna M; Fraaije, Marco W; Andrade, Leandro Helgueira
Source: Tetrahedron. Unidade: IQ
Subjects: SELÊNIO, LIPASE
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BRONDANI, Patricia Bulegon et al. Chemoenzymatic approaches to obtain chiral-centered selenium compounds. Tetrahedron, v. 68, n. 51, p. 10431-10436, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2012.09.087. Acesso em: 13 jun. 2025.
APA
Brondani, P. B., Guilmoto, N. M. A. de F., Dudek, H. M., Fraaije, M. W., & Andrade, L. H. (2012). Chemoenzymatic approaches to obtain chiral-centered selenium compounds. Tetrahedron, 68( 51), 10431-10436. doi:10.1016/j.tet.2012.09.087
NLM
Brondani PB, Guilmoto NMA de F, Dudek HM, Fraaije MW, Andrade LH. Chemoenzymatic approaches to obtain chiral-centered selenium compounds [Internet]. Tetrahedron. 2012 ; 68( 51): 10431-10436.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2012.09.087
Vancouver
Brondani PB, Guilmoto NMA de F, Dudek HM, Fraaije MW, Andrade LH. Chemoenzymatic approaches to obtain chiral-centered selenium compounds [Internet]. Tetrahedron. 2012 ; 68( 51): 10431-10436.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2012.09.087
Artigo de periodico
Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts (2012)
Sousa, Bruno Artur de; Keppler, Arthur Franz; Gariani, Rogério Aparecido; Comasseto, João Valdir; Santos, Alcindo Aparecido dos
Source: Tetrahedron. Unidade: IQ
Subjects: COMPOSTOS ORGANOMETÁLICOS, CALCOGÊNIOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOUSA, Bruno Artur de et al. Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts. Tetrahedron, v. 68, n. 51, p. 10406-10413, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2012.09.027. Acesso em: 13 jun. 2025.
APA
Sousa, B. A. de, Keppler, A. F., Gariani, R. A., Comasseto, J. V., & Santos, A. A. dos. (2012). Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts. Tetrahedron, 68( 51), 10406-10413. doi:10.1016/j.tet.2012.09.027
NLM
Sousa BA de, Keppler AF, Gariani RA, Comasseto JV, Santos AA dos. Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts [Internet]. Tetrahedron. 2012 ; 68( 51): 10406-10413.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2012.09.027
Vancouver
Sousa BA de, Keppler AF, Gariani RA, Comasseto JV, Santos AA dos. Metallic chalcogenolates mediated modular Michael-aldol cascade reaction: an easy route to multi-functionalized chalcogenides and Morita-Baylis-Hillman adducts [Internet]. Tetrahedron. 2012 ; 68( 51): 10406-10413.[citado 2025 jun. 13 ] Available from: https://doi.org/10.1016/j.tet.2012.09.027

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