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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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] 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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] 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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] 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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] 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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] 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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2018.10.019
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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] 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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] 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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] 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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] 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: 03 nov. 2024. , 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 2024 nov. 03 ] 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 2024 nov. 03 ] 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
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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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] 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
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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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] 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
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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: 03 nov. 2024. , 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 2024 nov. 03 ] 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 2024 nov. 03 ] 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
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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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] 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: 03 nov. 2024.
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 2024 nov. 03 ] 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 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2012.09.027
Artigo de periodico
Tellurium in organic synthesis: a general approach to buteno- and butanolides (2012)
Ferrarini, Renan dos Santos; Santos, Alcindo Aparecido dos ; Comasseto, João Valdir
Source: Tetrahedron. Unidade: IQ
Subjects: TELÚRIO, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERRARINI, Renan dos Santos e SANTOS, Alcindo Aparecido dos e COMASSETO, João Valdir. Tellurium in organic synthesis: a general approach to buteno- and butanolides. Tetrahedron, v. 68, n. 40, p. 10601-10610, 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2012.09.074. Acesso em: 03 nov. 2024.
APA
Ferrarini, R. dos S., Santos, A. A. dos, & Comasseto, J. V. (2012). Tellurium in organic synthesis: a general approach to buteno- and butanolides. Tetrahedron, 68( 40), 10601-10610. doi:10.1016/j.tet.2012.09.074
NLM
Ferrarini R dos S, Santos AA dos, Comasseto JV. Tellurium in organic synthesis: a general approach to buteno- and butanolides [Internet]. Tetrahedron. 2012 ; 68( 40): 10601-10610.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2012.09.074
Vancouver
Ferrarini R dos S, Santos AA dos, Comasseto JV. Tellurium in organic synthesis: a general approach to buteno- and butanolides [Internet]. Tetrahedron. 2012 ; 68( 40): 10601-10610.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2012.09.074
Artigo de periodico
An alternative approach for the synthesis of aryl-alkyl tellurides: reaction of aryl iodides with metal alkyltellurolates promoted by CuI (2011)
Silva, Márcio Santos da; Comasseto, João Valdir
Source: Tetrahedron. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, TELÚRIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Márcio Santos da e COMASSETO, João Valdir. An alternative approach for the synthesis of aryl-alkyl tellurides: reaction of aryl iodides with metal alkyltellurolates promoted by CuI. Tetrahedron, v. 67, n. 45, p. 8763-8768 : + Supplementary materials ( S1-S33), 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2011.09.014. Acesso em: 03 nov. 2024.
APA
Silva, M. S. da, & Comasseto, J. V. (2011). An alternative approach for the synthesis of aryl-alkyl tellurides: reaction of aryl iodides with metal alkyltellurolates promoted by CuI. Tetrahedron, 67( 45), 8763-8768 : + Supplementary materials ( S1-S33). doi:10.1016/j.tet.2011.09.014
NLM
Silva MS da, Comasseto JV. An alternative approach for the synthesis of aryl-alkyl tellurides: reaction of aryl iodides with metal alkyltellurolates promoted by CuI [Internet]. Tetrahedron. 2011 ; 67( 45): 8763-8768 : + Supplementary materials ( S1-S33).[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2011.09.014
Vancouver
Silva MS da, Comasseto JV. An alternative approach for the synthesis of aryl-alkyl tellurides: reaction of aryl iodides with metal alkyltellurolates promoted by CuI [Internet]. Tetrahedron. 2011 ; 67( 45): 8763-8768 : + Supplementary materials ( S1-S33).[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2011.09.014
Artigo de periodico
Synthesis of substituted 'alpha','beta'-unsaturated 'delta'-lactones from vinyl tellurides (2011)
Oliveira, Juliana M; Freitas, Juliano C. R; Comasseto, João Valdir; Menezes, Paulo Henrique
Source: Tetrahedron. Unidade: IQ
Subjects: SÍNTESE ORGÂNICA, PRODUTOS NATURAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
OLIVEIRA, Juliana M et al. Synthesis of substituted 'alpha','beta'-unsaturated 'delta'-lactones from vinyl tellurides. Tetrahedron, v. 67, n. 16, p. 3003-3009 : + supplementary materials ( S1-S47), 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2011.02.029. Acesso em: 03 nov. 2024.
APA
Oliveira, J. M., Freitas, J. C. R., Comasseto, J. V., & Menezes, P. H. (2011). Synthesis of substituted 'alpha','beta'-unsaturated 'delta'-lactones from vinyl tellurides. Tetrahedron, 67( 16), 3003-3009 : + supplementary materials ( S1-S47). doi:10.1016/j.tet.2011.02.029
NLM
Oliveira JM, Freitas JCR, Comasseto JV, Menezes PH. Synthesis of substituted 'alpha','beta'-unsaturated 'delta'-lactones from vinyl tellurides [Internet]. Tetrahedron. 2011 ; 67( 16): 3003-3009 : + supplementary materials ( S1-S47).[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2011.02.029
Vancouver
Oliveira JM, Freitas JCR, Comasseto JV, Menezes PH. Synthesis of substituted 'alpha','beta'-unsaturated 'delta'-lactones from vinyl tellurides [Internet]. Tetrahedron. 2011 ; 67( 16): 3003-3009 : + supplementary materials ( S1-S47).[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2011.02.029
Artigo de periodico
Glycoclusters presenting lactose on calix[4]arene cores display trypanocidal activity (2011)
Galante, Eva; Geraci, Corrada; Sciuto, Sebastiano; Campo, Vanessa Leiria; Carvalho, Ivone; Sesti-Costa, Renata; Guedes, Paulo Marcos da Matta; Silva, João Santana da; Hill, Lionel; Nepogodiev, Sergey A; Field, Robert A.
Source: Tetrahedron. Unidades: FCFRP, FMRP
Subjects: TRIPANOSSOMICIDAS, TECNOLOGIA FARMACÊUTICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
GALANTE, Eva et al. Glycoclusters presenting lactose on calix[4]arene cores display trypanocidal activity. Tetrahedron, v. 67, n. 33, p. 5902-5912, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2011.06.065. Acesso em: 03 nov. 2024.
APA
Galante, E., Geraci, C., Sciuto, S., Campo, V. L., Carvalho, I., Sesti-Costa, R., et al. (2011). Glycoclusters presenting lactose on calix[4]arene cores display trypanocidal activity. Tetrahedron, 67( 33), 5902-5912. doi:10.1016/j.tet.2011.06.065
NLM
Galante E, Geraci C, Sciuto S, Campo VL, Carvalho I, Sesti-Costa R, Guedes PM da M, Silva JS da, Hill L, Nepogodiev SA, Field RA. Glycoclusters presenting lactose on calix[4]arene cores display trypanocidal activity [Internet]. Tetrahedron. 2011 ; 67( 33): 5902-5912.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2011.06.065
Vancouver
Galante E, Geraci C, Sciuto S, Campo VL, Carvalho I, Sesti-Costa R, Guedes PM da M, Silva JS da, Hill L, Nepogodiev SA, Field RA. Glycoclusters presenting lactose on calix[4]arene cores display trypanocidal activity [Internet]. Tetrahedron. 2011 ; 67( 33): 5902-5912.[citado 2024 nov. 03 ] Available from: https://doi.org/10.1016/j.tet.2011.06.065

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