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Artigo de periodico
Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases (2021)
Santos, Thiago dos ; Orenha, Henrique Pereira; Murie, Valter Eduardo ; Vessecchi, Ricardo ; Clososki, Giuliano Cesar
Source: Organic Letters. Unidades: FFCLRP, FCFRP
Subjects: COMPOSTOS DE NITROGÊNIO, NITRILAS, QUÍMICA ORGÂNICA, COMPOSTOS HETEROCÍCLICOS
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ABNT
SANTOS, Thiago dos et al. Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases. Organic Letters, v. 23, n. 19, p. 7396-7400, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.1c02572. Acesso em: 05 dez. 2025.
APA
Santos, T. dos, Orenha, H. P., Murie, V. E., Vessecchi, R., & Clososki, G. C. (2021). Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases. Organic Letters, 23( 19), 7396-7400. doi:10.1021/acs.orglett.1c02572
NLM
Santos T dos, Orenha HP, Murie VE, Vessecchi R, Clososki GC. Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases [Internet]. Organic Letters. 2021 ; 23( 19): 7396-7400.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/acs.orglett.1c02572
Vancouver
Santos T dos, Orenha HP, Murie VE, Vessecchi R, Clososki GC. Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases [Internet]. Organic Letters. 2021 ; 23( 19): 7396-7400.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/acs.orglett.1c02572
Artigo de periodico
Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones (2020)
Santos, Thiago dos ; Grundke, Caroline; Lucas, Tobias; Großmann, Luca; Clososki, Giuliano Cesar ; Opatz, Till
Source: European Journal of Organic Chemistry. Unidade: FCFRP
Subjects: QUÍMICA ORGÂNICA, BIOMASSA, CARBOIDRATOS, GLICOSE
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ABNT
SANTOS, Thiago dos et al. Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones. European Journal of Organic Chemistry, v. 2020, n. 41, p. 6429-6432, 2020Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202000970. Acesso em: 05 dez. 2025.
APA
Santos, T. dos, Grundke, C., Lucas, T., Großmann, L., Clososki, G. C., & Opatz, T. (2020). Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones. European Journal of Organic Chemistry, 2020( 41), 6429-6432. doi:10.1002/ejoc.202000970
NLM
Santos T dos, Grundke C, Lucas T, Großmann L, Clososki GC, Opatz T. Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones [Internet]. European Journal of Organic Chemistry. 2020 ; 2020( 41): 6429-6432.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1002/ejoc.202000970
Vancouver
Santos T dos, Grundke C, Lucas T, Großmann L, Clososki GC, Opatz T. Glucose as an eco‐friendly reductant in a one‐pot synthesis of 2,3‐dihydroquinazolin‐4(1H)‐ones [Internet]. European Journal of Organic Chemistry. 2020 ; 2020( 41): 6429-6432.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1002/ejoc.202000970
Artigo de periodico
The preparation of benzyl esters using stoichiometric niobium (V) chloride versus niobium grafted SiO2 catalyst: A comparison study (2018)
Barbosa, Sandro L.; Lima, Camila D.; Almeida, Melina A. R.; Mourão, Larissa S.; Ottone, Myrlene; Nelson, David L.; Klein, Stanlei I.; Zanatta, Lucas D. ; Clososki, Giuliano Cesar ; Caires, Franco J. ; Nassar, Eduardo J.; Hurtado, Gabriela R.
Source: Heliyon. Unidades: FCFRP, FFCLRP
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, NIÓBIO, CARBONATOS
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ABNT
BARBOSA, Sandro L. et al. The preparation of benzyl esters using stoichiometric niobium (V) chloride versus niobium grafted SiO2 catalyst: A comparison study. Heliyon, v. 4, n. 3, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.heliyon.2018.e00571. Acesso em: 05 dez. 2025.
APA
Barbosa, S. L., Lima, C. D., Almeida, M. A. R., Mourão, L. S., Ottone, M., Nelson, D. L., et al. (2018). The preparation of benzyl esters using stoichiometric niobium (V) chloride versus niobium grafted SiO2 catalyst: A comparison study. Heliyon, 4( 3). doi:10.1016/j.heliyon.2018.e00571
NLM
Barbosa SL, Lima CD, Almeida MAR, Mourão LS, Ottone M, Nelson DL, Klein SI, Zanatta LD, Clososki GC, Caires FJ, Nassar EJ, Hurtado GR. The preparation of benzyl esters using stoichiometric niobium (V) chloride versus niobium grafted SiO2 catalyst: A comparison study [Internet]. Heliyon. 2018 ; 4( 3):[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.heliyon.2018.e00571
Vancouver
Barbosa SL, Lima CD, Almeida MAR, Mourão LS, Ottone M, Nelson DL, Klein SI, Zanatta LD, Clososki GC, Caires FJ, Nassar EJ, Hurtado GR. The preparation of benzyl esters using stoichiometric niobium (V) chloride versus niobium grafted SiO2 catalyst: A comparison study [Internet]. Heliyon. 2018 ; 4( 3):[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.heliyon.2018.e00571
Artigo de periodico
Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl (2017)
Bozzini, Leandro A; Batista, João H. C.; Mello, Murilo B. M. de; Vessecchi, Ricardo; Clososki, Giuliano Cesar
Source: Tetrahedron Letters. Unidades: FFCLRP, FCFRP
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, PRODUTOS NATURAIS
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ABNT
BOZZINI, Leandro A et al. Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl. Tetrahedron Letters, v. 58, p. 4186-4190, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2017.09.051. Acesso em: 05 dez. 2025.
APA
Bozzini, L. A., Batista, J. H. C., Mello, M. B. M. de, Vessecchi, R., & Clososki, G. C. (2017). Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl. Tetrahedron Letters, 58, 4186-4190. doi:10.1016/j.tetlet.2017.09.051
NLM
Bozzini LA, Batista JHC, Mello MBM de, Vessecchi R, Clososki GC. Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl [Internet]. Tetrahedron Letters. 2017 ; 58 4186-4190.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.tetlet.2017.09.051
Vancouver
Bozzini LA, Batista JHC, Mello MBM de, Vessecchi R, Clososki GC. Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl [Internet]. Tetrahedron Letters. 2017 ; 58 4186-4190.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.tetlet.2017.09.051
Artigo de periodico
Extractive biocatalysis in the asymmetric reduction of α-alkyl, β-aryl enones by Baker's yeast (2017)
Silva, Rafaela M.; Okano, Laura Tiemi; Rodrigues, J. Augusto R.; Clososki, Giuliano Cesar
Source: Tetrahedron : Asymmetry. Unidades: FCFRP, FFCLRP
Subjects: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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ABNT
SILVA, Rafaela M. et al. Extractive biocatalysis in the asymmetric reduction of α-alkyl, β-aryl enones by Baker's yeast. Tetrahedron : Asymmetry, v. 28, p. 939-944, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2017.05.009. Acesso em: 05 dez. 2025.
APA
Silva, R. M., Okano, L. T., Rodrigues, J. A. R., & Clososki, G. C. (2017). Extractive biocatalysis in the asymmetric reduction of α-alkyl, β-aryl enones by Baker's yeast. Tetrahedron : Asymmetry, 28, 939-944. doi:10.1016/j.tetasy.2017.05.009
NLM
Silva RM, Okano LT, Rodrigues JAR, Clososki GC. Extractive biocatalysis in the asymmetric reduction of α-alkyl, β-aryl enones by Baker's yeast [Internet]. Tetrahedron : Asymmetry. 2017 ; 28 939-944.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.tetasy.2017.05.009
Vancouver
Silva RM, Okano LT, Rodrigues JAR, Clososki GC. Extractive biocatalysis in the asymmetric reduction of α-alkyl, β-aryl enones by Baker's yeast [Internet]. Tetrahedron : Asymmetry. 2017 ; 28 939-944.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.tetasy.2017.05.009
Artigo de periodico
Directed functionalization of halophenyl-2-oxazolines with TMPMgCl.LiCl (2015)
Batista, João H. C.; Santos, Fernanda M. dos; Bozzini, Leandro A.; Vessecchi, Ricardo; Oliveira, Alfredo Ricardo Marques de; Clososki, Giuliano Cesar
Source: European Journal of Organic Chemistry. Unidades: FFCLRP, FCFRP
Subjects: QUÍMICA ORGÂNICA, MAGNÉSIO, SÍNTESE ORGÂNICA
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ABNT
BATISTA, João H. C. et al. Directed functionalization of halophenyl-2-oxazolines with TMPMgCl.LiCl. European Journal of Organic Chemistry, v. 2015, n. 5, p. 967-977, 2015Tradução . . Disponível em: https://doi.org/10.1002/ejoc.201403255. Acesso em: 05 dez. 2025.
APA
Batista, J. H. C., Santos, F. M. dos, Bozzini, L. A., Vessecchi, R., Oliveira, A. R. M. de, & Clososki, G. C. (2015). Directed functionalization of halophenyl-2-oxazolines with TMPMgCl.LiCl. European Journal of Organic Chemistry, 2015( 5), 967-977. doi:10.1002/ejoc.201403255
NLM
Batista JHC, Santos FM dos, Bozzini LA, Vessecchi R, Oliveira ARM de, Clososki GC. Directed functionalization of halophenyl-2-oxazolines with TMPMgCl.LiCl [Internet]. European Journal of Organic Chemistry. 2015 ; 2015( 5): 967-977.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1002/ejoc.201403255
Vancouver
Batista JHC, Santos FM dos, Bozzini LA, Vessecchi R, Oliveira ARM de, Clososki GC. Directed functionalization of halophenyl-2-oxazolines with TMPMgCl.LiCl [Internet]. European Journal of Organic Chemistry. 2015 ; 2015( 5): 967-977.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1002/ejoc.201403255
Artigo de periodico
Directed metalation of 1-ester-substituted indolizines: base/electrophile-controlled regioselective functionalization (2015)
Amaral, Mônica F. Z. J.; Baumgartner, Amanda A.; Vessecchi, Ricardo; Clososki, Giuliano Cesar
Source: Organic Letters. Unidades: FFCLRP, FCFRP
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
AMARAL, Mônica F. Z. J. et al. Directed metalation of 1-ester-substituted indolizines: base/electrophile-controlled regioselective functionalization. Organic Letters, v. 17, n. 2, p. 238–241, 2015Tradução . . Disponível em: https://doi.org/10.1021/ol503288e. Acesso em: 05 dez. 2025.
APA
Amaral, M. F. Z. J., Baumgartner, A. A., Vessecchi, R., & Clososki, G. C. (2015). Directed metalation of 1-ester-substituted indolizines: base/electrophile-controlled regioselective functionalization. Organic Letters, 17( 2), 238–241. doi:10.1021/ol503288e
NLM
Amaral MFZJ, Baumgartner AA, Vessecchi R, Clososki GC. Directed metalation of 1-ester-substituted indolizines: base/electrophile-controlled regioselective functionalization [Internet]. Organic Letters. 2015 ; 17( 2): 238–241.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/ol503288e
Vancouver
Amaral MFZJ, Baumgartner AA, Vessecchi R, Clososki GC. Directed metalation of 1-ester-substituted indolizines: base/electrophile-controlled regioselective functionalization [Internet]. Organic Letters. 2015 ; 17( 2): 238–241.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/ol503288e
Artigo de periodico
Highly enantioselective acylation of chlorohydrins using Amano AK lipase from P. fluorescens immobilized on silk fibroin–alginate spheres (2014)
Ferreira, Irlon Maciel; Nishimura, Rodolfo H. V.; Souza, Ana Beatriz dos Anjos; Clososki, Giuliano Cesar; Yoshioka, Sergio Akinobu ; Porto, Andre Luiz Meleiro
Source: Tetrahedron Letters. Unidades: FCFRP, IQSC
Subjects: ENZIMAS, QUÍMICA ORGÂNICA
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ABNT
FERREIRA, Irlon Maciel et al. Highly enantioselective acylation of chlorohydrins using Amano AK lipase from P. fluorescens immobilized on silk fibroin–alginate spheres. Tetrahedron Letters, v. 55, n. 7, p. 5062-5065, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2014.07.032. Acesso em: 05 dez. 2025.
APA
Ferreira, I. M., Nishimura, R. H. V., Souza, A. B. dos A., Clososki, G. C., Yoshioka, S. A., & Porto, A. L. M. (2014). Highly enantioselective acylation of chlorohydrins using Amano AK lipase from P. fluorescens immobilized on silk fibroin–alginate spheres. Tetrahedron Letters, 55( 7), 5062-5065. doi:10.1016/j.tetlet.2014.07.032
NLM
Ferreira IM, Nishimura RHV, Souza AB dos A, Clososki GC, Yoshioka SA, Porto ALM. Highly enantioselective acylation of chlorohydrins using Amano AK lipase from P. fluorescens immobilized on silk fibroin–alginate spheres [Internet]. Tetrahedron Letters. 2014 ; 55( 7): 5062-5065.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.tetlet.2014.07.032
Vancouver
Ferreira IM, Nishimura RHV, Souza AB dos A, Clososki GC, Yoshioka SA, Porto ALM. Highly enantioselective acylation of chlorohydrins using Amano AK lipase from P. fluorescens immobilized on silk fibroin–alginate spheres [Internet]. Tetrahedron Letters. 2014 ; 55( 7): 5062-5065.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.tetlet.2014.07.032
Trabalho de evento-resumo periodico
Directed metalation of aromatic aldimines using Li/Mg-TMP amides (2013)
Cavalcante Silva, S.; Batista, J. H.; Moraes, F.; Pereira, N. de A.; Clososki, Giuliano Cesar
Source: Blucher Chemistry Proceedings. Conference titles: Brazilian Meeting on Organic Synthesis (BMOS). Unidade: FCFRP
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
CAVALCANTE SILVA, S. et al. Directed metalation of aromatic aldimines using Li/Mg-TMP amides. Blucher Chemistry Proceedings. São Paulo: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo. . Acesso em: 05 dez. 2025. , 2013
APA
Cavalcante Silva, S., Batista, J. H., Moraes, F., Pereira, N. de A., & Clososki, G. C. (2013). Directed metalation of aromatic aldimines using Li/Mg-TMP amides. Blucher Chemistry Proceedings. São Paulo: Faculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo.
NLM
Cavalcante Silva S, Batista JH, Moraes F, Pereira N de A, Clososki GC. Directed metalation of aromatic aldimines using Li/Mg-TMP amides. Blucher Chemistry Proceedings. 2013 ; 1( 2):[citado 2025 dez. 05 ]
Vancouver
Cavalcante Silva S, Batista JH, Moraes F, Pereira N de A, Clososki GC. Directed metalation of aromatic aldimines using Li/Mg-TMP amides. Blucher Chemistry Proceedings. 2013 ; 1( 2):[citado 2025 dez. 05 ]

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