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Artigo de periodico
Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted (2018)
Oliveira, Isadora M. de; Darbem, Mariana P; Esteves, Carlos Henrique Alves; Pimenta, Daniel C; Schpector, Júlio Zukerman; Stefani, Hélio Alexandre ; Manarin, Flávia
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: ITÉRBIO, SÍNTESE ORGÂNICA
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ABNT
OLIVEIRA, Isadora M. de et al. Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted. Tetrahedron Letters, v. 59, n. 24, p. 3907-3911, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2018.09.022. Acesso em: 08 out. 2024.
APA
Oliveira, I. M. de, Darbem, M. P., Esteves, C. H. A., Pimenta, D. C., Schpector, J. Z., Stefani, H. A., & Manarin, F. (2018). Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted. Tetrahedron Letters, 59( 24), 3907-3911. doi:10.1016/j.tetlet.2018.09.022
NLM
Oliveira IM de, Darbem MP, Esteves CHA, Pimenta DC, Schpector JZ, Stefani HA, Manarin F. Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted [Internet]. Tetrahedron Letters. 2018 ; 59( 24): 3907-3911.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2018.09.022
Vancouver
Oliveira IM de, Darbem MP, Esteves CHA, Pimenta DC, Schpector JZ, Stefani HA, Manarin F. Ytterbium-catalyzed formal [4+2] cycloaddition: synthesis of chalcogen-quinolines 3-unsubstituted [Internet]. Tetrahedron Letters. 2018 ; 59( 24): 3907-3911.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2018.09.022
Artigo de periodico
Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization (2017)
Shamim, Anwar; Souza, Frederico Bernardes de; Vasconcelos, Stanley Nunes Siqueira; Stefani, Hélio Alexandre
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: SÍNTESE ORGÂNICA, COBRE
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ABNT
SHAMIM, Anwar et al. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization. Tetrahedron Letters, v. 58, n. 9, p. 884-888, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2017.01.059. Acesso em: 08 out. 2024.
APA
Shamim, A., Souza, F. B. de, Vasconcelos, S. N. S., & Stefani, H. A. (2017). Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization. Tetrahedron Letters, 58( 9), 884-888. doi:10.1016/j.tetlet.2017.01.059
NLM
Shamim A, Souza FB de, Vasconcelos SNS, Stefani HA. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization [Internet]. Tetrahedron Letters. 2017 ; 58( 9): 884-888.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.059
Vancouver
Shamim A, Souza FB de, Vasconcelos SNS, Stefani HA. Synthesis of a library of glucal-derived triazoles via copper-catalyzed azide-alkyne cyclization [Internet]. Tetrahedron Letters. 2017 ; 58( 9): 884-888.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.059
Artigo de periodico
Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition (2017)
Souza, Frederico Bernardes de; Vasconcelos, Stanley Nunes Siqueira; Reis, Joel Savi dos; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: SÍNTESE ORGÂNICA, COBRE
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ABNT
SOUZA, Frederico Bernardes de et al. Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition. Tetrahedron Letters, v. 58, n. 11, p. 1057-1060, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2017.01.107. Acesso em: 08 out. 2024.
APA
Souza, F. B. de, Vasconcelos, S. N. S., Reis, J. S. dos, Pimenta, D. C., & Stefani, H. A. (2017). Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition. Tetrahedron Letters, 58( 11), 1057-1060. doi:10.1016/j.tetlet.2017.01.107
NLM
Souza FB de, Vasconcelos SNS, Reis JS dos, Pimenta DC, Stefani HA. Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition [Internet]. Tetrahedron Letters. 2017 ; 58( 11): 1057-1060.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.107
Vancouver
Souza FB de, Vasconcelos SNS, Reis JS dos, Pimenta DC, Stefani HA. Synthesis and functionalization of N-sulfinyl imines: sonogashira reaction and copper-catalyzed azide-alkyne cycloaddition [Internet]. Tetrahedron Letters. 2017 ; 58( 11): 1057-1060.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.107
Artigo de periodico
Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles (2016)
Souza, Frederico B; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: TECNOLOGIA DE MICRO-ONDAS, ALDEÍDOS
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ABNT
SOUZA, Frederico B e PIMENTA, Daniel Carvalho e STEFANI, Hélio Alexandre. Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles. Tetrahedron Letters, v. 57, n. 14, p. 1592-1596, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2016.02.105. Acesso em: 08 out. 2024.
APA
Souza, F. B., Pimenta, D. C., & Stefani, H. A. (2016). Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles. Tetrahedron Letters, 57( 14), 1592-1596. doi:10.1016/j.tetlet.2016.02.105
NLM
Souza FB, Pimenta DC, Stefani HA. Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles [Internet]. Tetrahedron Letters. 2016 ; 57( 14): 1592-1596.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2016.02.105
Vancouver
Souza FB, Pimenta DC, Stefani HA. Microwave-assisted one-pot three-component synthesis of imine 1,2,3-triazoles [Internet]. Tetrahedron Letters. 2016 ; 57( 14): 1592-1596.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2016.02.105
Artigo de periodico
Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization (2015)
Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Ali, Bakhat; Madureira, Lucas Sousa; Zukerman-Schpector, Júlio; Stefani, Hélio Alexandre
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: COMPOSTOS HETEROCÍCLICOS, PALÁDIO
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ABNT
SHAMIM, Anwar et al. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization. Tetrahedron Letters, v. 56, n. 43, p. 5836-5842, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.08.052. Acesso em: 08 out. 2024.
APA
Shamim, A., Vasconcelos, S. N. S., Ali, B., Madureira, L. S., Zukerman-Schpector, J., & Stefani, H. A. (2015). Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization. Tetrahedron Letters, 56( 43), 5836-5842. doi:10.1016/j.tetlet.2015.08.052
NLM
Shamim A, Vasconcelos SNS, Ali B, Madureira LS, Zukerman-Schpector J, Stefani HA. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization [Internet]. Tetrahedron Letters. 2015 ; 56( 43): 5836-5842.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052
Vancouver
Shamim A, Vasconcelos SNS, Ali B, Madureira LS, Zukerman-Schpector J, Stefani HA. Ligand and copper free Sonogashira coupling to achieve 2-alkynyl D-glucal derivatives: regioselective electrophile promoted nucleophilic 5-endo-dig cyclization [Internet]. Tetrahedron Letters. 2015 ; 56( 43): 5836-5842.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2015.08.052
Artigo de periodico
Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones (2015)
Ali, Bakhat; Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Stefani, Hélio Alexandre
Fonte: Tetrahedron Letters. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
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ABNT
ALI, Bakhat et al. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones. Tetrahedron Letters, v. 56, n. 28, p. 4234-4241, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.05.066. Acesso em: 08 out. 2024.
APA
Ali, B., Shamim, A., Vasconcelos, S. N. S., & Stefani, H. A. (2015). Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones. Tetrahedron Letters, 56( 28), 4234-4241. doi:10.1016/j.tetlet.2015.05.066
NLM
Ali B, Shamim A, Vasconcelos SNS, Stefani HA. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones [Internet]. Tetrahedron Letters. 2015 ; 56( 28): 4234-4241.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2015.05.066
Vancouver
Ali B, Shamim A, Vasconcelos SNS, Stefani HA. Synthesis and applications of 4-substituted 1-(4-iodophenyl)pyrrolidine-2,5-diones [Internet]. Tetrahedron Letters. 2015 ; 56( 28): 4234-4241.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2015.05.066
Artigo de periodico
Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes (2015)
Ali, Bakhat; Schpector, Júlio Zukerman; Ferreira, Fernando P; Shamim, Anwar; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: AMINAS, CATÁLISE
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ABNT
ALI, Bakhat et al. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes. Tetrahedron Letters, v. 56, n. 9, p. 1153-1158, 2015Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2015.01.059. Acesso em: 08 out. 2024.
APA
Ali, B., Schpector, J. Z., Ferreira, F. P., Shamim, A., Pimenta, D. C., & Stefani, H. A. (2015). Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes. Tetrahedron Letters, 56( 9), 1153-1158. doi:10.1016/j.tetlet.2015.01.059
NLM
Ali B, Schpector JZ, Ferreira FP, Shamim A, Pimenta DC, Stefani HA. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes [Internet]. Tetrahedron Letters. 2015 ; 56( 9): 1153-1158.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059
Vancouver
Ali B, Schpector JZ, Ferreira FP, Shamim A, Pimenta DC, Stefani HA. Lewis-acid catalyzed N-acyliminium ion cyclodimerization: synthesis of symmetrical 1,4-dioxanes [Internet]. Tetrahedron Letters. 2015 ; 56( 9): 1153-1158.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2015.01.059
Artigo de periodico
Synthesis of functionalized N-triazolyl maleimides (2014)
Stefani, Hélio Alexandre ; Ferreira, Fernando P; Ali, Bakhat; Pimenta, Daniel Carvalho
Fonte: Tetrahedron Letters. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
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ABNT
STEFANI, Hélio Alexandre et al. Synthesis of functionalized N-triazolyl maleimides. Tetrahedron Letters, v. 55, n. 31, p. 4355-4358, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2014.05.095. Acesso em: 08 out. 2024.
APA
Stefani, H. A., Ferreira, F. P., Ali, B., & Pimenta, D. C. (2014). Synthesis of functionalized N-triazolyl maleimides. Tetrahedron Letters, 55( 31), 4355-4358. doi:10.1016/j.tetlet.2014.05.095
NLM
Stefani HA, Ferreira FP, Ali B, Pimenta DC. Synthesis of functionalized N-triazolyl maleimides [Internet]. Tetrahedron Letters. 2014 ; 55( 31): 4355-4358.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2014.05.095
Vancouver
Stefani HA, Ferreira FP, Ali B, Pimenta DC. Synthesis of functionalized N-triazolyl maleimides [Internet]. Tetrahedron Letters. 2014 ; 55( 31): 4355-4358.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2014.05.095
Artigo de periodico
Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction (2013)
Stefani, Hélio Alexandre ; Silva, Nathália Cristina da Silva e; Vasconcelos, Stanley Nunes Siqueira; Manarin, Flávia; Souza, Frederico B
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: TELÚRIO, SÍNTESE ORGÂNICA
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ABNT
STEFANI, Hélio Alexandre et al. Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction. Tetrahedron Letters, v. 54, n. 22, p. 2809-2812, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2013.03.061. Acesso em: 08 out. 2024.
APA
Stefani, H. A., Silva, N. C. da S. e, Vasconcelos, S. N. S., Manarin, F., & Souza, F. B. (2013). Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction. Tetrahedron Letters, 54( 22), 2809-2812. doi:10.1016/j.tetlet.2013.03.061
NLM
Stefani HA, Silva NC da S e, Vasconcelos SNS, Manarin F, Souza FB. Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction [Internet]. Tetrahedron Letters. 2013 ; 54( 22): 2809-2812.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2013.03.061
Vancouver
Stefani HA, Silva NC da S e, Vasconcelos SNS, Manarin F, Souza FB. Functionalization of 5-telluro-1,2,3-triazoles: Te/Li exchange and Suzuki-Miyaura cross-coupling reaction [Internet]. Tetrahedron Letters. 2013 ; 54( 22): 2809-2812.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2013.03.061
Artigo de periodico
One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles (2013)
Stefani, Hélio Alexandre ; Vasconcelos, Stanley Nunes Siqueira; Souza, Frederico B; Manarin, Flávia; Zukerman-Schpector, Júlio
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
STEFANI, Hélio Alexandre et al. One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles. Tetrahedron Letters, v. 54, n. 43, p. 5821-5825, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2013.08.064. Acesso em: 08 out. 2024.
APA
Stefani, H. A., Vasconcelos, S. N. S., Souza, F. B., Manarin, F., & Zukerman-Schpector, J. (2013). One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles. Tetrahedron Letters, 54( 43), 5821-5825. doi:10.1016/j.tetlet.2013.08.064
NLM
Stefani HA, Vasconcelos SNS, Souza FB, Manarin F, Zukerman-Schpector J. One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles [Internet]. Tetrahedron Letters. 2013 ; 54( 43): 5821-5825.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.064
Vancouver
Stefani HA, Vasconcelos SNS, Souza FB, Manarin F, Zukerman-Schpector J. One-pot three-component synthesis of indole-3-glyoxyl derivatives and indole-3-glyoxyl triazoles [Internet]. Tetrahedron Letters. 2013 ; 54( 43): 5821-5825.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.064
Artigo de periodico
Synthesis of alpha-alkenyl-alpha-amino esters via addition of potassium Alkenyltrifluoroborate salts to imine in the presence of Yb`(OTf) IND. 3´ (2013)
Stefani, Hélio Alexandre ; Khan, AMNA N; Manarin, Flávia; Vendramini, Pedro H; Eberlin, Marcos Nogueira
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: AMINOÁCIDOS, ITÉRBIO
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ABNT
STEFANI, Hélio Alexandre et al. Synthesis of alpha-alkenyl-alpha-amino esters via addition of potassium Alkenyltrifluoroborate salts to imine in the presence of Yb`(OTf) IND. 3´. Tetrahedron Letters, v. 54, n. 46, p. 6204-6207, 2013Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2013.08.133. Acesso em: 08 out. 2024.
APA
Stefani, H. A., Khan, A. M. N. A. N., Manarin, F., Vendramini, P. H., & Eberlin, M. N. (2013). Synthesis of alpha-alkenyl-alpha-amino esters via addition of potassium Alkenyltrifluoroborate salts to imine in the presence of Yb`(OTf) IND. 3´. Tetrahedron Letters, 54( 46), 6204-6207. doi:10.1016/j.tetlet.2013.08.133
NLM
Stefani HA, Khan AMNAN, Manarin F, Vendramini PH, Eberlin MN. Synthesis of alpha-alkenyl-alpha-amino esters via addition of potassium Alkenyltrifluoroborate salts to imine in the presence of Yb`(OTf) IND. 3´ [Internet]. Tetrahedron Letters. 2013 ; 54( 46): 6204-6207.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.133
Vancouver
Stefani HA, Khan AMNAN, Manarin F, Vendramini PH, Eberlin MN. Synthesis of alpha-alkenyl-alpha-amino esters via addition of potassium Alkenyltrifluoroborate salts to imine in the presence of Yb`(OTf) IND. 3´ [Internet]. Tetrahedron Letters. 2013 ; 54( 46): 6204-6207.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2013.08.133
Artigo de periodico
Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction (2012)
Stefani, Hélio Alexandre ; Silva, Nathália Cristina da Silva e; Manarin, Flávia; Lüdtke, Diogo, Seibert; Zukerman-Schpector, Júlio; Madureira, Lucas Sousa; Tiekink, Edward R. T
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
STEFANI, Hélio Alexandre et al. Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction. Tetrahedron Letters, v. 53, n. 14, p. 1742-1747 : + Supplementary materials ( S1-S36), 2012Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2012.01.102. Acesso em: 08 out. 2024.
APA
Stefani, H. A., Silva, N. C. da S. e, Manarin, F., Lüdtke, D., Zukerman-Schpector, J., Madureira, L. S., & Tiekink, E. R. T. (2012). Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction. Tetrahedron Letters, 53( 14), 1742-1747 : + Supplementary materials ( S1-S36). doi:10.1016/j.tetlet.2012.01.102
NLM
Stefani HA, Silva NC da S e, Manarin F, Lüdtke D, Zukerman-Schpector J, Madureira LS, Tiekink ERT. Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction [Internet]. Tetrahedron Letters. 2012 ; 53( 14): 1742-1747 : + Supplementary materials ( S1-S36).[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2012.01.102
Vancouver
Stefani HA, Silva NC da S e, Manarin F, Lüdtke D, Zukerman-Schpector J, Madureira LS, Tiekink ERT. Synthesis of 1,2,3-triazolylpyranosides through click chemistry reaction [Internet]. Tetrahedron Letters. 2012 ; 53( 14): 1742-1747 : + Supplementary materials ( S1-S36).[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2012.01.102
Artigo de periodico
Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles (2011)
Stefani, Hélio Alexandre ; Vieira, Adriano Siqueira; Amaral, Monica Franco Zanini Junqueira; Cooper, Leora
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: POTÁSSIO, SÍNTESE ORGÂNICA
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ABNT
STEFANI, Hélio Alexandre et al. Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles. Tetrahedron Letters, v. 52, n. 33, p. 4256-4261 + Supplementary Materials ( S1-S7), 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.04.072. Acesso em: 08 out. 2024.
APA
Stefani, H. A., Vieira, A. S., Amaral, M. F. Z. J., & Cooper, L. (2011). Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles. Tetrahedron Letters, 52( 33), 4256-4261 + Supplementary Materials ( S1-S7). doi:10.1016/j.tetlet.2011.04.072
NLM
Stefani HA, Vieira AS, Amaral MFZJ, Cooper L. Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles [Internet]. Tetrahedron Letters. 2011 ; 52( 33): 4256-4261 + Supplementary Materials ( S1-S7).[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2011.04.072
Vancouver
Stefani HA, Vieira AS, Amaral MFZJ, Cooper L. Synthesis of 5-alkynyl-2,2,6-trimethyl-1,3-dioxin-4-ones and 1,4-disubstituted-1,2,3-triazoles [Internet]. Tetrahedron Letters. 2011 ; 52( 33): 4256-4261 + Supplementary Materials ( S1-S7).[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2011.04.072
Artigo de periodico
Synthesis of (2S)-isopropyl-5-alkynylpyrimidin-2-ones: precursors of 'beta'-aminoacids (2011)
Stefani, Hélio Alexandre ; Amaral, Monica Franco Zanini Junqueira; Juaristi, Eusebio
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: AMINOÁCIDOS, SÍNTESE ORGÂNICA
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ABNT
STEFANI, Hélio Alexandre e AMARAL, Monica Franco Zanini Junqueira e JUARISTI, Eusebio. Synthesis of (2S)-isopropyl-5-alkynylpyrimidin-2-ones: precursors of 'beta'-aminoacids. Tetrahedron Letters, v. 52, n. 9, p. 1014-1019, 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2010.12.087. Acesso em: 08 out. 2024.
APA
Stefani, H. A., Amaral, M. F. Z. J., & Juaristi, E. (2011). Synthesis of (2S)-isopropyl-5-alkynylpyrimidin-2-ones: precursors of 'beta'-aminoacids. Tetrahedron Letters, 52( 9), 1014-1019. doi:10.1016/j.tetlet.2010.12.087
NLM
Stefani HA, Amaral MFZJ, Juaristi E. Synthesis of (2S)-isopropyl-5-alkynylpyrimidin-2-ones: precursors of 'beta'-aminoacids [Internet]. Tetrahedron Letters. 2011 ; 52( 9): 1014-1019.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2010.12.087
Vancouver
Stefani HA, Amaral MFZJ, Juaristi E. Synthesis of (2S)-isopropyl-5-alkynylpyrimidin-2-ones: precursors of 'beta'-aminoacids [Internet]. Tetrahedron Letters. 2011 ; 52( 9): 1014-1019.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2010.12.087
Artigo de periodico
Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions (2011)
Stefani, Hélio Alexandre ; Amaral, Mônica Franco Zannini Junqueira; Manarin, Flávia; Ando, Rômulo Augusto ; Silva, Nathalia Cristina S; Juaristi, Eusebio
Fonte: Tetrahedron Letters. Unidades: FCF, IQ
Assuntos: QUÍMICA VERDE, COMPOSTOS HETEROCÍCLICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions. Tetrahedron Letters, v. 52, n. 51, p. 6883-6886 : + Supplementary materials ( S1-S6), 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.10.011. Acesso em: 08 out. 2024.
APA
Stefani, H. A., Amaral, M. F. Z. J., Manarin, F., Ando, R. A., Silva, N. C. S., & Juaristi, E. (2011). Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions. Tetrahedron Letters, 52( 51), 6883-6886 : + Supplementary materials ( S1-S6). doi:10.1016/j.tetlet.2011.10.011
NLM
Stefani HA, Amaral MFZJ, Manarin F, Ando RA, Silva NCS, Juaristi E. Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions [Internet]. Tetrahedron Letters. 2011 ; 52( 51): 6883-6886 : + Supplementary materials ( S1-S6).[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2011.10.011
Vancouver
Stefani HA, Amaral MFZJ, Manarin F, Ando RA, Silva NCS, Juaristi E. Functionalization of 2-(S)-isopropyl-5-iodo-pyrimidin-4-ones through 'CU'(I)-mediated 1,3-dipolar azide–alkyne cycloadditions [Internet]. Tetrahedron Letters. 2011 ; 52( 51): 6883-6886 : + Supplementary materials ( S1-S6).[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2011.10.011
Artigo de periodico
Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition (2011)
Stefani, Hélio Alexandre ; Canduzini, Hugo A; Manarin, Flávia
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: ULTRASSOM, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre e CANDUZINI, Hugo A e MANARIN, Flávia. Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition. Tetrahedron Letters, v. 52, n. 46, p. 6086-6090 : + Supplementary materials ( S1-S10), 2011Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2011.09.004. Acesso em: 08 out. 2024.
APA
Stefani, H. A., Canduzini, H. A., & Manarin, F. (2011). Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition. Tetrahedron Letters, 52( 46), 6086-6090 : + Supplementary materials ( S1-S10). doi:10.1016/j.tetlet.2011.09.004
NLM
Stefani HA, Canduzini HA, Manarin F. Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition [Internet]. Tetrahedron Letters. 2011 ; 52( 46): 6086-6090 : + Supplementary materials ( S1-S10).[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2011.09.004
Vancouver
Stefani HA, Canduzini HA, Manarin F. Modular synthesis of mono, di, and tri-1,4-disubstituted-1,2,3-triazoles through copper-mediated alkyne-azide cycloaddition [Internet]. Tetrahedron Letters. 2011 ; 52( 46): 6086-6090 : + Supplementary materials ( S1-S10).[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2011.09.004
Artigo de periodico
Ultrasound-assisted synthesis of symmetrical biaryls by palladium-catalyzed detelluration of 1,2-diarylditellanes (2010)
Singh, Fateh Veer; Stefani, Hélio Alexandre
Fonte: Tetrahedron Letters. Unidade: FCF
Assuntos: ULTRASSONOGRAFIA, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SINGH, Fateh Veer e STEFANI, Hélio Alexandre. Ultrasound-assisted synthesis of symmetrical biaryls by palladium-catalyzed detelluration of 1,2-diarylditellanes. Tetrahedron Letters, v. 51, n. 5, p. 863-867, 2010Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.12.028. Acesso em: 08 out. 2024.
APA
Singh, F. V., & Stefani, H. A. (2010). Ultrasound-assisted synthesis of symmetrical biaryls by palladium-catalyzed detelluration of 1,2-diarylditellanes. Tetrahedron Letters, 51( 5), 863-867. doi:10.1016/j.tetlet.2009.12.028
NLM
Singh FV, Stefani HA. Ultrasound-assisted synthesis of symmetrical biaryls by palladium-catalyzed detelluration of 1,2-diarylditellanes [Internet]. Tetrahedron Letters. 2010 ; 51( 5): 863-867.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2009.12.028
Vancouver
Singh FV, Stefani HA. Ultrasound-assisted synthesis of symmetrical biaryls by palladium-catalyzed detelluration of 1,2-diarylditellanes [Internet]. Tetrahedron Letters. 2010 ; 51( 5): 863-867.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2009.12.028
Artigo de periodico
One-post synthesis of 'alpha', 'beta'-epoxy ketones by palladium-catalyzed epoxidation-oxidation of terminal allylic alcohols (2010)
Singh, Fateh Veer; Pena, Jesus Marcelo; Stefani, Hélio Alexandre
Fonte: Tetrahedron Letters. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SINGH, Fateh Veer e PENA, Jesus Marcelo e STEFANI, Hélio Alexandre. One-post synthesis of 'alpha', 'beta'-epoxy ketones by palladium-catalyzed epoxidation-oxidation of terminal allylic alcohols. Tetrahedron Letters, v. 51, n. 13, p. 1671-1673, 2010Tradução . . Disponível em: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6THS-4Y95X5B-1-1T&_cdi=5290&_user=5674931&_pii=S0040403910001139&_orig=browse&_coverDate=03%2F31%2F2010&_sk=999489986&view=c&wchp=dGLzVlz-zSkzV&md5=25577e83567dc0204da783595aab9b68&ie=/sdarticle.pdf. Acesso em: 08 out. 2024.
APA
Singh, F. V., Pena, J. M., & Stefani, H. A. (2010). One-post synthesis of 'alpha', 'beta'-epoxy ketones by palladium-catalyzed epoxidation-oxidation of terminal allylic alcohols. Tetrahedron Letters, 51( 13), 1671-1673. Recuperado de http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6THS-4Y95X5B-1-1T&_cdi=5290&_user=5674931&_pii=S0040403910001139&_orig=browse&_coverDate=03%2F31%2F2010&_sk=999489986&view=c&wchp=dGLzVlz-zSkzV&md5=25577e83567dc0204da783595aab9b68&ie=/sdarticle.pdf
NLM
Singh FV, Pena JM, Stefani HA. One-post synthesis of 'alpha', 'beta'-epoxy ketones by palladium-catalyzed epoxidation-oxidation of terminal allylic alcohols [Internet]. Tetrahedron Letters. 2010 ; 51( 13): 1671-1673.[citado 2024 out. 08 ] Available from: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6THS-4Y95X5B-1-1T&_cdi=5290&_user=5674931&_pii=S0040403910001139&_orig=browse&_coverDate=03%2F31%2F2010&_sk=999489986&view=c&wchp=dGLzVlz-zSkzV&md5=25577e83567dc0204da783595aab9b68&ie=/sdarticle.pdf
Vancouver
Singh FV, Pena JM, Stefani HA. One-post synthesis of 'alpha', 'beta'-epoxy ketones by palladium-catalyzed epoxidation-oxidation of terminal allylic alcohols [Internet]. Tetrahedron Letters. 2010 ; 51( 13): 1671-1673.[citado 2024 out. 08 ] Available from: http://www.sciencedirect.com/science?_ob=MImg&_imagekey=B6THS-4Y95X5B-1-1T&_cdi=5290&_user=5674931&_pii=S0040403910001139&_orig=browse&_coverDate=03%2F31%2F2010&_sk=999489986&view=c&wchp=dGLzVlz-zSkzV&md5=25577e83567dc0204da783595aab9b68&ie=/sdarticle.pdf
Artigo de periodico
Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides (2009)
Singh, Fateh Veer; Amaral, Mônica F. Z. J.; Stefani, Hélio Alexandre
Fonte: Tetrahedron Letters. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SINGH, Fateh Veer e AMARAL, Mônica F. Z. J. e STEFANI, Hélio Alexandre. Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides. Tetrahedron Letters, v. 50, n. 22, p. 2636-2639, 2009Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2009.03.078. Acesso em: 08 out. 2024.
APA
Singh, F. V., Amaral, M. F. Z. J., & Stefani, H. A. (2009). Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides. Tetrahedron Letters, 50( 22), 2636-2639. doi:10.1016/j.tetlet.2009.03.078
NLM
Singh FV, Amaral MFZJ, Stefani HA. Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides [Internet]. Tetrahedron Letters. 2009 ; 50( 22): 2636-2639.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.078
Vancouver
Singh FV, Amaral MFZJ, Stefani HA. Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides [Internet]. Tetrahedron Letters. 2009 ; 50( 22): 2636-2639.[citado 2024 out. 08 ] Available from: https://doi.org/10.1016/j.tetlet.2009.03.078
Artigo de periodico
Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides (2009)
Stefani, Hélio Alexandre ; Pena, Jesus Marcelo; Gueogjian, Kemilla; Petragnani, Nicola; Vaz, Boniek Gontijo; Eberlin, Marcos Nogueira
Fonte: Tetrahedron Letters. Unidades: FCF, IQ
Assuntos: SÍNTESE ORGÂNICA, TELÚRIO, PALÁDIO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
STEFANI, Hélio Alexandre et al. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters, v. 50, n. 40, p. 5589-5595, 2009Tradução . . Acesso em: 08 out. 2024.
APA
Stefani, H. A., Pena, J. M., Gueogjian, K., Petragnani, N., Vaz, B. G., & Eberlin, M. N. (2009). Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters, 50( 40), 5589-5595.
NLM
Stefani HA, Pena JM, Gueogjian K, Petragnani N, Vaz BG, Eberlin MN. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters. 2009 ; 50( 40): 5589-5595.[citado 2024 out. 08 ]
Vancouver
Stefani HA, Pena JM, Gueogjian K, Petragnani N, Vaz BG, Eberlin MN. Synthesis of 'alpha','beta'-unsaturated aryl esters via Heck reaction of unsymmetrical aryl tellurides. Tetrahedron Letters. 2009 ; 50( 40): 5589-5595.[citado 2024 out. 08 ]

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