ReP USP - Resultado da busca

Artigo de periodico
Organoselenium has a potent fungicidal effect on Cryptococcus neoformans and inhibits the virulence factors (2023)
Jesus, Daniel Felipe Freitas de ; Freitas, Aline Luiza Duarte de; Oliveira, Isadora Maria de ; Almeida, Larissa Costa de ; Bastos, Rafael Wesley; Spadari, Cristina de Castro ; Melo, Analy Salles de Azevedo ; Santos, Daniel de Assis ; Reis, Flavia C. G; Rodrigues, Márcio Lourenço ; Lotufo, Leticia Veras Costa ; Stefani, Hélio Alexandre ; Ishida, Kelly
Source: Antimicrobial Agents and Chemotherapy. Unidades: ICB, FCF, BIOTECNOLOGIA, IQ
Subjects: ANTIFÚNGICOS, FUNGICIDAS, CRYPTOCOCCUS NEOFORMANS, VIRULÊNCIA, FUNGOS MITOSPORICOS, FUNGICIDAS INDUSTRIAIS, TRAÇAS, MICOSES, MICROBIOLOGIA, FARMACOLOGIA, LARVA
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ABNT
JESUS, Daniel Felipe Freitas de et al. Organoselenium has a potent fungicidal effect on Cryptococcus neoformans and inhibits the virulence factors. Antimicrobial Agents and Chemotherapy, v. 67, n. 3, p. 1-16, 2023Tradução . . Disponível em: https://doi.org/10.1128/aac.00759-22. Acesso em: 25 maio 2024.
APA
Jesus, D. F. F. de, Freitas, A. L. D. de, Oliveira, I. M. de, Almeida, L. C. de, Bastos, R. W., Spadari, C. de C., et al. (2023). Organoselenium has a potent fungicidal effect on Cryptococcus neoformans and inhibits the virulence factors. Antimicrobial Agents and Chemotherapy, 67( 3), 1-16. doi:10.1128/aac.00759-22
NLM
Jesus DFF de, Freitas ALD de, Oliveira IM de, Almeida LC de, Bastos RW, Spadari C de C, Melo AS de A, Santos D de A, Reis FCG, Rodrigues ML, Lotufo LVC, Stefani HA, Ishida K. Organoselenium has a potent fungicidal effect on Cryptococcus neoformans and inhibits the virulence factors [Internet]. Antimicrobial Agents and Chemotherapy. 2023 ; 67( 3): 1-16.[citado 2024 maio 25 ] Available from: https://doi.org/10.1128/aac.00759-22
Vancouver
Jesus DFF de, Freitas ALD de, Oliveira IM de, Almeida LC de, Bastos RW, Spadari C de C, Melo AS de A, Santos D de A, Reis FCG, Rodrigues ML, Lotufo LVC, Stefani HA, Ishida K. Organoselenium has a potent fungicidal effect on Cryptococcus neoformans and inhibits the virulence factors [Internet]. Antimicrobial Agents and Chemotherapy. 2023 ; 67( 3): 1-16.[citado 2024 maio 25 ] Available from: https://doi.org/10.1128/aac.00759-22
Artigo de periodico
Synthesis and phytotoxic evaluation of 3-Indolylglycine derivatives as new natural-like herbicides (2023)
Amaral, Alexandra A; Willig, Julia C. M; Olguin, Conceição F. A ; Oliveira, Isadora Maria de ; Stefani, Hélio Alexandre ; Botteselle, Giancarlo V ; Manarin, Flávia
Source: Journal of the Brazilian Chemical Society. Unidades: FCF, IQ
Subjects: HERBICIDAS, FITOTOXICIDADE
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ABNT
AMARAL, Alexandra A et al. Synthesis and phytotoxic evaluation of 3-Indolylglycine derivatives as new natural-like herbicides. Journal of the Brazilian Chemical Society, v. 34, n. 10, p. 1464-1473, 2023Tradução . . Disponível em: https://doi.org/10.21577/0103-5053.20230058. Acesso em: 25 maio 2024.
APA
Amaral, A. A., Willig, J. C. M., Olguin, C. F. A., Oliveira, I. M. de, Stefani, H. A., Botteselle, G. V., & Manarin, F. (2023). Synthesis and phytotoxic evaluation of 3-Indolylglycine derivatives as new natural-like herbicides. Journal of the Brazilian Chemical Society, 34( 10), 1464-1473. doi:10.21577/0103-5053.20230058
NLM
Amaral AA, Willig JCM, Olguin CFA, Oliveira IM de, Stefani HA, Botteselle GV, Manarin F. Synthesis and phytotoxic evaluation of 3-Indolylglycine derivatives as new natural-like herbicides [Internet]. Journal of the Brazilian Chemical Society. 2023 ; 34( 10): 1464-1473.[citado 2024 maio 25 ] Available from: https://doi.org/10.21577/0103-5053.20230058
Vancouver
Amaral AA, Willig JCM, Olguin CFA, Oliveira IM de, Stefani HA, Botteselle GV, Manarin F. Synthesis and phytotoxic evaluation of 3-Indolylglycine derivatives as new natural-like herbicides [Internet]. Journal of the Brazilian Chemical Society. 2023 ; 34( 10): 1464-1473.[citado 2024 maio 25 ] Available from: https://doi.org/10.21577/0103-5053.20230058
Trabalho de evento-resumo
Spectroscopic characterization and cytotoxicity evaluation of a library of urea-based compounds (2022)
Damiano, Gabrielle Silva; Souza, Laura Francisca Leite do Prado de; Lopes, Rayssa de Mello ; Paulino, Antonio Augusto Soares ; Stefani, Hélio Alexandre ; Rodrigues, Tiago
Source: Abstract Book. Conference titles: Annual Meeting of the Brazilian Society for Biochemistry and Molecular Biology/SBBq. Unidade: FCF
Subjects: PROTEÍNAS QUINASES, QUIMIOTERAPIA
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ABNT
DAMIANO, Gabrielle Silva et al. Spectroscopic characterization and cytotoxicity evaluation of a library of urea-based compounds. 2022, Anais.. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular, 2022. Disponível em: https://www2.sbbq.org.br/reuniao/2022/images/livro_completo.pdf. Acesso em: 25 maio 2024.
APA
Damiano, G. S., Souza, L. F. L. do P. de, Lopes, R. de M., Paulino, A. A. S., Stefani, H. A., & Rodrigues, T. (2022). Spectroscopic characterization and cytotoxicity evaluation of a library of urea-based compounds. In Abstract Book. São Paulo: Sociedade Brasileira de Bioquímica e Biologia Molecular. Recuperado de https://www2.sbbq.org.br/reuniao/2022/images/livro_completo.pdf
NLM
Damiano GS, Souza LFL do P de, Lopes R de M, Paulino AAS, Stefani HA, Rodrigues T. Spectroscopic characterization and cytotoxicity evaluation of a library of urea-based compounds [Internet]. Abstract Book. 2022 ;[citado 2024 maio 25 ] Available from: https://www2.sbbq.org.br/reuniao/2022/images/livro_completo.pdf
Vancouver
Damiano GS, Souza LFL do P de, Lopes R de M, Paulino AAS, Stefani HA, Rodrigues T. Spectroscopic characterization and cytotoxicity evaluation of a library of urea-based compounds [Internet]. Abstract Book. 2022 ;[citado 2024 maio 25 ] Available from: https://www2.sbbq.org.br/reuniao/2022/images/livro_completo.pdf
Artigo de periodico
Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction (2022)
Jesus, Jéssica Carol de; Noguchi, Henrique Kenich ; Toledo, Mônica Franco Zannini Junqueira ; Burrow, Robert A ; Pimenta, Daniel C. ; Stefani, Hélio Alexandre
Source: European Journal of Organic Chemistry. Unidade: FCF
Subjects: AMINOÁCIDOS, PROTEÍNAS, AMIDAS
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ABNT
JESUS, Jéssica Carol de et al. Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction. European Journal of Organic Chemistry, v. 2022, n. 30, p. 1-7 art. e202200332, 2022Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202200332. Acesso em: 25 maio 2024.
APA
Jesus, J. C. de, Noguchi, H. K., Toledo, M. F. Z. J., Burrow, R. A., Pimenta, D. C., & Stefani, H. A. (2022). Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction. European Journal of Organic Chemistry, 2022( 30), 1-7 art. e202200332. doi:10.1002/ejoc.202200332
NLM
Jesus JC de, Noguchi HK, Toledo MFZJ, Burrow RA, Pimenta DC, Stefani HA. Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction [Internet]. European Journal of Organic Chemistry. 2022 ; 2022( 30): 1-7 art. e202200332.[citado 2024 maio 25 ] Available from: https://doi.org/10.1002/ejoc.202200332
Vancouver
Jesus JC de, Noguchi HK, Toledo MFZJ, Burrow RA, Pimenta DC, Stefani HA. Synthesis of glycal amides from amino acid esters by carbonylative coupling reaction [Internet]. European Journal of Organic Chemistry. 2022 ; 2022( 30): 1-7 art. e202200332.[citado 2024 maio 25 ] Available from: https://doi.org/10.1002/ejoc.202200332
Trabalho de evento-resumo
Aminocarbonilação de glical com ésteres de aminoácidos via reações de acoplamento carbonilativo (2022)
Noguchi, Henrique Kenich ; Jesus, Jéssica Carol de; Stefani, Hélio Alexandre
Source: Resumos. Conference titles: Simpósio Internacional de Iniciação Cientifíca e Tecnológica da USP/SIICUSP. Unidade: FCF
Subjects: QUÍMICA ORGÂNICA, AMINOÁCIDOS
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ABNT
NOGUCHI, Henrique Kenich e JESUS, Jéssica Carol de e STEFANI, Hélio Alexandre. Aminocarbonilação de glical com ésteres de aminoácidos via reações de acoplamento carbonilativo. 2022, Anais.. São Paulo: Pró-Reitoria de Pesquisa da USP, 2022. Disponível em: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210. Acesso em: 25 maio 2024.
APA
Noguchi, H. K., Jesus, J. C. de, & Stefani, H. A. (2022). Aminocarbonilação de glical com ésteres de aminoácidos via reações de acoplamento carbonilativo. In Resumos. São Paulo: Pró-Reitoria de Pesquisa da USP. Recuperado de https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
NLM
Noguchi HK, Jesus JC de, Stefani HA. Aminocarbonilação de glical com ésteres de aminoácidos via reações de acoplamento carbonilativo [Internet]. Resumos. 2022 ;[citado 2024 maio 25 ] Available from: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
Vancouver
Noguchi HK, Jesus JC de, Stefani HA. Aminocarbonilação de glical com ésteres de aminoácidos via reações de acoplamento carbonilativo [Internet]. Resumos. 2022 ;[citado 2024 maio 25 ] Available from: https://uspdigital.usp.br/siicusp/siicPublicacao.jsp?codmnu=7210
Artigo de periodico
Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction (2022)
Darbem, Mariana P; Esteves, Henrique A; Burrow, Robert A ; Paulino, Antonio Augusto Soares ; Pimenta, Daniel Carvalho ; Stefani, Hélio Alexandre
Source: RSC Advances. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
DARBEM, Mariana P et al. Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction. RSC Advances, v. 12, p. 2145–2149, 2022Tradução . . Disponível em: https://doi.org/10.1039/d1ra08388k. Acesso em: 25 maio 2024.
APA
Darbem, M. P., Esteves, H. A., Burrow, R. A., Paulino, A. A. S., Pimenta, D. C., & Stefani, H. A. (2022). Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction. RSC Advances, 12, 2145–2149. doi:10.1039/d1ra08388k
NLM
Darbem MP, Esteves HA, Burrow RA, Paulino AAS, Pimenta DC, Stefani HA. Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction [Internet]. RSC Advances. 2022 ; 12 2145–2149.[citado 2024 maio 25 ] Available from: https://doi.org/10.1039/d1ra08388k
Vancouver
Darbem MP, Esteves HA, Burrow RA, Paulino AAS, Pimenta DC, Stefani HA. Synthesis of unprotected glyco-alkynones via molybdenum-catalyzed carbonylative Sonogashira cross-coupling reaction [Internet]. RSC Advances. 2022 ; 12 2145–2149.[citado 2024 maio 25 ] Available from: https://doi.org/10.1039/d1ra08388k
Artigo de periodico
Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study (2021)
Veloso, Rodolpho Rebello; Shamim, Anwar ; Lamarre, Yann Ives; Stefani, Hélio Alexandre ; Sciani, Juliana Mozer
Source: Bioorganic Chemistry. Unidades: FCF, IQSC, FMRP
Subjects: ANEMIA FALCIFORME, ANTIOXIDANTES
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ABNT
VELOSO, Rodolpho Rebello et al. Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study. Bioorganic Chemistry, v. 109, p. 104709, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2021.104709. Acesso em: 25 maio 2024.
APA
Veloso, R. R., Shamim, A., Lamarre, Y. I., Stefani, H. A., & Sciani, J. M. (2021). Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study. Bioorganic Chemistry, 109, 104709. doi:10.1016/j.bioorg.2021.104709
NLM
Veloso RR, Shamim A, Lamarre YI, Stefani HA, Sciani JM. Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study [Internet]. Bioorganic Chemistry. 2021 ;109 104709.[citado 2024 maio 25 ] Available from: https://doi.org/10.1016/j.bioorg.2021.104709
Vancouver
Veloso RR, Shamim A, Lamarre YI, Stefani HA, Sciani JM. Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study [Internet]. Bioorganic Chemistry. 2021 ;109 104709.[citado 2024 maio 25 ] Available from: https://doi.org/10.1016/j.bioorg.2021.104709
Artigo de periodico
Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential (2020)
Costa, Claudia A; Lopes, Rayssa M; Ferraz, Letícia Silva; Esteves, Gabriela N. N; Di Iorio, Juliana F; Souza, Aline A; Oliveira, Isadora M. de; Manarin, Flávia ; Judice, Wagner Alves de Souza; Stefani, Hélio Alexandre ; Rodrigues, Tiago
Source: Bioorganic & Medicinal Chemistry. Unidade: FCF
Subjects: ANTINEOPLÁSICOS, ANTIPROTOZOÁRIOS, APOPTOSE
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ABNT
COSTA, Claudia A et al. Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential. Bioorganic & Medicinal Chemistry, v. 28, p. 1-13 art. 115511, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2020.115511. Acesso em: 25 maio 2024.
APA
Costa, C. A., Lopes, R. M., Ferraz, L. S., Esteves, G. N. N., Di Iorio, J. F., Souza, A. A., et al. (2020). Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential. Bioorganic & Medicinal Chemistry, 28, 1-13 art. 115511. doi:10.1016/j.bmc.2020.115511
NLM
Costa CA, Lopes RM, Ferraz LS, Esteves GNN, Di Iorio JF, Souza AA, Oliveira IM de, Manarin F, Judice WA de S, Stefani HA, Rodrigues T. Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential [Internet]. Bioorganic & Medicinal Chemistry. 2020 ; 28 1-13 art. 115511.[citado 2024 maio 25 ] Available from: https://doi.org/10.1016/j.bmc.2020.115511
Vancouver
Costa CA, Lopes RM, Ferraz LS, Esteves GNN, Di Iorio JF, Souza AA, Oliveira IM de, Manarin F, Judice WA de S, Stefani HA, Rodrigues T. Cytotoxicity of 4-substituted quinoline derivatives: Anticancer and antileishmanial potential [Internet]. Bioorganic & Medicinal Chemistry. 2020 ; 28 1-13 art. 115511.[citado 2024 maio 25 ] Available from: https://doi.org/10.1016/j.bmc.2020.115511
Artigo de periodico
Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals (2020)
Paulino, Antonio Augusto Soares ; Stefani, Hélio Alexandre
Source: European Journal of Organic Chemistry. Unidade: FCF
Subjects: UREIA, PALÁDIO, GLICOCONJUGADOS
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ABNT
PAULINO, Antonio Augusto Soares e STEFANI, Hélio Alexandre. Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals. European Journal of Organic Chemistry, v. 2020, p. 3847–3855, 2020Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202000494. Acesso em: 25 maio 2024.
APA
Paulino, A. A. S., & Stefani, H. A. (2020). Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals. European Journal of Organic Chemistry, 2020, 3847–3855. doi:10.1002/ejoc.202000494
NLM
Paulino AAS, Stefani HA. Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 3847–3855.[citado 2024 maio 25 ] Available from: https://doi.org/10.1002/ejoc.202000494
Vancouver
Paulino AAS, Stefani HA. Synthesis of diverse C2-glyco-acyl azides and -ureas by palladium-catalyzed carbonylation coupling of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 3847–3855.[citado 2024 maio 25 ] Available from: https://doi.org/10.1002/ejoc.202000494
Artigo de periodico
Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor (2020)
Paulino, Antonio Augusto Soares; Giroldo, Lilian; Pradie, Noriberto Araújo; Reis, Joel Savi dos; Back, Davi F; Braga, Ataualpa Albert Carmo ; Stefani, Hélio Alexandre ; Lodeiro, Carlos; Santos, Alcindo Aparecido dos
Source: Dyes and Pigments. Unidades: IQ, FCF
Subjects: SELÊNIO, PALÁDIO, FLUORESCÊNCIA
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ABNT
PAULINO, Antonio Augusto Soares et al. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor. Dyes and Pigments, v. 179, p. 1-10 art. 108355, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2020.108355. Acesso em: 25 maio 2024.
APA
Paulino, A. A. S., Giroldo, L., Pradie, N. A., Reis, J. S. dos, Back, D. F., Braga, A. A. C., et al. (2020). Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor. Dyes and Pigments, 179, 1-10 art. 108355. doi:10.1016/j.dyepig.2020.108355
NLM
Paulino AAS, Giroldo L, Pradie NA, Reis JS dos, Back DF, Braga AAC, Stefani HA, Lodeiro C, Santos AA dos. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor [Internet]. Dyes and Pigments. 2020 ; 179 1-10 art. 108355.[citado 2024 maio 25 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108355
Vancouver
Paulino AAS, Giroldo L, Pradie NA, Reis JS dos, Back DF, Braga AAC, Stefani HA, Lodeiro C, Santos AA dos. Nanomolar detection of palladium (II) through a novel seleno-rhodamine-based fluorescent and colorimetric chemosensor [Internet]. Dyes and Pigments. 2020 ; 179 1-10 art. 108355.[citado 2024 maio 25 ] Available from: https://doi.org/10.1016/j.dyepig.2020.108355
Artigo de periodico
α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals (2020)
Darbem, Mariana P; Esteves, Henrique A; Oliveira, Isadora Maria de ; Stefani, Hélio Alexandre
Source: European Journal of Organic Chemistry. Unidades: FCF, IQ
Subjects: GLICOSÍDEOS, PALÁDIO
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ABNT
DARBEM, Mariana P et al. α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals. European Journal of Organic Chemistry, v. 2020, p. 5220–5226, 2020Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202000846. Acesso em: 25 maio 2024.
APA
Darbem, M. P., Esteves, H. A., Oliveira, I. M. de, & Stefani, H. A. (2020). α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals. European Journal of Organic Chemistry, 2020, 5220–5226. doi:10.1002/ejoc.202000846
NLM
Darbem MP, Esteves HA, Oliveira IM de, Stefani HA. α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 5220–5226.[citado 2024 maio 25 ] Available from: https://doi.org/10.1002/ejoc.202000846
Vancouver
Darbem MP, Esteves HA, Oliveira IM de, Stefani HA. α,β-unsaturated 2-ketoglycosides via Pd-catalyzed carbonylative heck reaction of 2-iodoglycals [Internet]. European Journal of Organic Chemistry. 2020 ; 2020 5220–5226.[citado 2024 maio 25 ] Available from: https://doi.org/10.1002/ejoc.202000846
Artigo de periodico
A comparative study between Cu(INA)(2)-MOF and [Cu(INA)(2)(H2O)(4)] complex for a click reaction and the Biginelli reaction under solvent-free conditions (2020)
Willing, Julia C. Mansano; Granetto, Gustavo; Reginato, Danielly; Dutra, Felipe R; Poruczinski, Erica Fernanda; Oliveira, Isadora Maria de ; Stefani, Hélio Alexandre ; de Campos, Silvia D; Campos, Elvio A. de; Manarin, Flávia ; Botteselle, Giancarlo, V
Source: RSC Advances. Unidade: FCF
Subjects: CATÁLISE, COBRE
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ABNT
WILLING, Julia C. Mansano et al. A comparative study between Cu(INA)(2)-MOF and [Cu(INA)(2)(H2O)(4)] complex for a click reaction and the Biginelli reaction under solvent-free conditions. RSC Advances, v. 10, n. 6, p. 3407-3415, 2020Tradução . . Disponível em: https://doi.org/10.1039/c9ra10171c. Acesso em: 25 maio 2024.
APA
Willing, J. C. M., Granetto, G., Reginato, D., Dutra, F. R., Poruczinski, E. F., Oliveira, I. M. de, et al. (2020). A comparative study between Cu(INA)(2)-MOF and [Cu(INA)(2)(H2O)(4)] complex for a click reaction and the Biginelli reaction under solvent-free conditions. RSC Advances, 10( 6), 3407-3415. doi:10.1039/c9ra10171c
NLM
Willing JCM, Granetto G, Reginato D, Dutra FR, Poruczinski EF, Oliveira IM de, Stefani HA, de Campos SD, Campos EA de, Manarin F, Botteselle G. A comparative study between Cu(INA)(2)-MOF and [Cu(INA)(2)(H2O)(4)] complex for a click reaction and the Biginelli reaction under solvent-free conditions [Internet]. RSC Advances. 2020 ; 10( 6): 3407-3415.[citado 2024 maio 25 ] Available from: https://doi.org/10.1039/c9ra10171c
Vancouver
Willing JCM, Granetto G, Reginato D, Dutra FR, Poruczinski EF, Oliveira IM de, Stefani HA, de Campos SD, Campos EA de, Manarin F, Botteselle G. A comparative study between Cu(INA)(2)-MOF and [Cu(INA)(2)(H2O)(4)] complex for a click reaction and the Biginelli reaction under solvent-free conditions [Internet]. RSC Advances. 2020 ; 10( 6): 3407-3415.[citado 2024 maio 25 ] Available from: https://doi.org/10.1039/c9ra10171c
Artigo de periodico
Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals (2020)
Darbem, Mariana P; Esteves, Henrique A; Oliveira, Isadora Maria de ; Pimenta, Daniel Carvalho ; Stefani, Hélio Alexandre
Source: ChemCatChem. Unidades: BIOTECNOLOGIA, FCF, IQ
Subjects: PALÁDIO, HIDRÓLISE
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ABNT
DARBEM, Mariana P et al. Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals. ChemCatChem, v. 12, n. 2, p. 576-583, 2020Tradução . . Disponível em: https://doi.org/10.1002/cctc.201901403. Acesso em: 25 maio 2024.
APA
Darbem, M. P., Esteves, H. A., Oliveira, I. M. de, Pimenta, D. C., & Stefani, H. A. (2020). Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals. ChemCatChem, 12( 2), 576-583. doi:10.1002/cctc.201901403
NLM
Darbem MP, Esteves HA, Oliveira IM de, Pimenta DC, Stefani HA. Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals [Internet]. ChemCatChem. 2020 ; 12( 2): 576-583.[citado 2024 maio 25 ] Available from: https://doi.org/10.1002/cctc.201901403
Vancouver
Darbem MP, Esteves HA, Oliveira IM de, Pimenta DC, Stefani HA. Palladium-catalyzed thio- and selenocarbonylation of 2-iodoglycals [Internet]. ChemCatChem. 2020 ; 12( 2): 576-583.[citado 2024 maio 25 ] Available from: https://doi.org/10.1002/cctc.201901403
Artigo de periodico
Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers (2020)
Oliveira, Isadora Maria de ; Esteves, Henrique A; Darbem, Mariana P; Sartorelli, Arthur; Correra, Thiago Carita ; Oliveira, Andre F. Rodrigues ; Pimenta, Daniel C; Zukerman-Schpector, Júlio ; Stefani, Hélio Alexandre
Source: ChemCatChem. Unidades: FCF, IQ
Subjects: LIGANTES, CATALISADORES
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ABNT
OLIVEIRA, Isadora Maria de et al. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers. ChemCatChem, v. 12, p. 3545–3552, 2020Tradução . . Disponível em: https://doi.org/10.1002/cctc.202000395. Acesso em: 25 maio 2024.
APA
Oliveira, I. M. de, Esteves, H. A., Darbem, M. P., Sartorelli, A., Correra, T. C., Oliveira, A. F. R., et al. (2020). Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers. ChemCatChem, 12, 3545–3552. doi:10.1002/cctc.202000395
NLM
Oliveira IM de, Esteves HA, Darbem MP, Sartorelli A, Correra TC, Oliveira AFR, Pimenta DC, Zukerman-Schpector J, Stefani HA. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers [Internet]. ChemCatChem. 2020 ; 12 3545–3552.[citado 2024 maio 25 ] Available from: https://doi.org/10.1002/cctc.202000395
Vancouver
Oliveira IM de, Esteves HA, Darbem MP, Sartorelli A, Correra TC, Oliveira AFR, Pimenta DC, Zukerman-Schpector J, Stefani HA. Stereo- and regioselective Cu-catalyzed hydroboration of alkynyl chalcogenoethers [Internet]. ChemCatChem. 2020 ; 12 3545–3552.[citado 2024 maio 25 ] Available from: https://doi.org/10.1002/cctc.202000395
Artigo de periodico
Novel 2-Aryloxazoline compounds exhibit an inhibitory effect on Candida spp., including antifungal-resistant isolates (2020)
Argomedo, Luis Miguel Zaravia; Barroso, Vinicius de Morais; Barreiro, Cristiane de Souza; Rocha, Mariana Pompilio Darbem ; Ishida, Kelly ; Stefani, Hélio Alexandre
Source: ACS Medicinal Chemistry Letters. Unidades: ICB, FCF
Subjects: MICROBIOLOGIA, ANTIFÚNGICOS, MICOLOGIA MÉDICA, CANDIDA, ASPERGILLUS, CITOTOXINAS
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ABNT
ARGOMEDO, Luis Miguel Zaravia et al. Novel 2-Aryloxazoline compounds exhibit an inhibitory effect on Candida spp., including antifungal-resistant isolates. ACS Medicinal Chemistry Letters, v. 11, n. 12, p. 2470–2475, 2020Tradução . . Disponível em: https://doi.org/10.1021/acsmedchemlett.0c00449. Acesso em: 25 maio 2024.
APA
Argomedo, L. M. Z., Barroso, V. de M., Barreiro, C. de S., Rocha, M. P. D., Ishida, K., & Stefani, H. A. (2020). Novel 2-Aryloxazoline compounds exhibit an inhibitory effect on Candida spp., including antifungal-resistant isolates. ACS Medicinal Chemistry Letters, 11( 12), 2470–2475. doi:10.1021/acsmedchemlett.0c00449
NLM
Argomedo LMZ, Barroso V de M, Barreiro C de S, Rocha MPD, Ishida K, Stefani HA. Novel 2-Aryloxazoline compounds exhibit an inhibitory effect on Candida spp., including antifungal-resistant isolates [Internet]. ACS Medicinal Chemistry Letters. 2020 ; 11( 12): 2470–2475.[citado 2024 maio 25 ] Available from: https://doi.org/10.1021/acsmedchemlett.0c00449
Vancouver
Argomedo LMZ, Barroso V de M, Barreiro C de S, Rocha MPD, Ishida K, Stefani HA. Novel 2-Aryloxazoline compounds exhibit an inhibitory effect on Candida spp., including antifungal-resistant isolates [Internet]. ACS Medicinal Chemistry Letters. 2020 ; 11( 12): 2470–2475.[citado 2024 maio 25 ] Available from: https://doi.org/10.1021/acsmedchemlett.0c00449
Artigo de periodico
Synthesis, structure study, first-principles investigations and luminescence properties of europium and terbium complexes (2020)
Ali, Bakhat; Stefani, Hélio Alexandre ; Imran, Muhammad; Irfan, Ahmad; Assiri, Mohammed A; Felinto, Maria Claudia França da Cunha; Khalid, Muhammad; Al-Sehemi, Abdullah G
Source: Journal of Fluorescence. Unidades: FCF, IPEN
Subjects: LUMINESCÊNCIA, EURÓPIO, TÉRBIO
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ABNT
ALI, Bakhat et al. Synthesis, structure study, first-principles investigations and luminescence properties of europium and terbium complexes. Journal of Fluorescence, v. 30, p. 1345–1355, 2020Tradução . . Disponível em: https://doi.org/10.1007/s10895-020-02613-z. Acesso em: 25 maio 2024.
APA
Ali, B., Stefani, H. A., Imran, M., Irfan, A., Assiri, M. A., Felinto, M. C. F. da C., et al. (2020). Synthesis, structure study, first-principles investigations and luminescence properties of europium and terbium complexes. Journal of Fluorescence, 30, 1345–1355. doi:10.1007/s10895-020-02613-z
NLM
Ali B, Stefani HA, Imran M, Irfan A, Assiri MA, Felinto MCF da C, Khalid M, Al-Sehemi AG. Synthesis, structure study, first-principles investigations and luminescence properties of europium and terbium complexes [Internet]. Journal of Fluorescence. 2020 ; 30 1345–1355.[citado 2024 maio 25 ] Available from: https://doi.org/10.1007/s10895-020-02613-z
Vancouver
Ali B, Stefani HA, Imran M, Irfan A, Assiri MA, Felinto MCF da C, Khalid M, Al-Sehemi AG. Synthesis, structure study, first-principles investigations and luminescence properties of europium and terbium complexes [Internet]. Journal of Fluorescence. 2020 ; 30 1345–1355.[citado 2024 maio 25 ] Available from: https://doi.org/10.1007/s10895-020-02613-z
Trabalho de evento-resumo
Antibacterial activity of selenoquinolines against Staphylococcus aureus (2019)
Santos, Milena Noronha dos; Oliveira, Isadora Maria de; Manarim, Flavia; Stefani, Hélio Alexandre ; Wiggers, Helton José; Cheleski, Juliana
Source: Resumos. Conference titles: Reunião Anual da Sociedade Brasileira de Química/SBQ. Unidade: FCF
Subjects: STAPHYLOCOCCUS, BACTERICIDAS
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ABNT
SANTOS, Milena Noronha dos et al. Antibacterial activity of selenoquinolines against Staphylococcus aureus. 2019, Anais.. São Paulo: Sociedade Brasileira de Química/SBQ, 2019. Disponível em: http://www.sbq.org.br/42ra/anexos/42RASBQ_programa_e_resumos.pdf. Acesso em: 25 maio 2024.
APA
Santos, M. N. dos, Oliveira, I. M. de, Manarim, F., Stefani, H. A., Wiggers, H. J., & Cheleski, J. (2019). Antibacterial activity of selenoquinolines against Staphylococcus aureus. In Resumos. São Paulo: Sociedade Brasileira de Química/SBQ. Recuperado de http://www.sbq.org.br/42ra/anexos/42RASBQ_programa_e_resumos.pdf
NLM
Santos MN dos, Oliveira IM de, Manarim F, Stefani HA, Wiggers HJ, Cheleski J. Antibacterial activity of selenoquinolines against Staphylococcus aureus [Internet]. Resumos. 2019 ;[citado 2024 maio 25 ] Available from: http://www.sbq.org.br/42ra/anexos/42RASBQ_programa_e_resumos.pdf
Vancouver
Santos MN dos, Oliveira IM de, Manarim F, Stefani HA, Wiggers HJ, Cheleski J. Antibacterial activity of selenoquinolines against Staphylococcus aureus [Internet]. Resumos. 2019 ;[citado 2024 maio 25 ] Available from: http://www.sbq.org.br/42ra/anexos/42RASBQ_programa_e_resumos.pdf
Artigo de periodico
Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution (2019)
Santos, Fabiano S; Zanotto, Gabriel M; Argomedo, Luiz M. Z; Darbem, Mariana P; Gonçalves, Paulo F. B; Stefani, Hélio Alexandre ; Rodembusch, Fabiano S
Source: Dyes and Pigments. Unidade: FCF
Subjects: SENSORES ÓPTICOS, SÍNTESE ORGÂNICA
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ABNT
SANTOS, Fabiano S et al. Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution. Dyes and Pigments, v. 165, p. 372-382, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.dyepig.2019.02.047. Acesso em: 25 maio 2024.
APA
Santos, F. S., Zanotto, G. M., Argomedo, L. M. Z., Darbem, M. P., Gonçalves, P. F. B., Stefani, H. A., & Rodembusch, F. S. (2019). Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution. Dyes and Pigments, 165, 372-382. doi:10.1016/j.dyepig.2019.02.047
NLM
Santos FS, Zanotto GM, Argomedo LMZ, Darbem MP, Gonçalves PFB, Stefani HA, Rodembusch FS. Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution [Internet]. Dyes and Pigments. 2019 ; 165 372-382.[citado 2024 maio 25 ] Available from: https://doi.org/10.1016/j.dyepig.2019.02.047
Vancouver
Santos FS, Zanotto GM, Argomedo LMZ, Darbem MP, Gonçalves PFB, Stefani HA, Rodembusch FS. Synthesis, experimental and theoretical photophysical study of proton transfer based oxazoline fluorophores. Potential tailor made optical sensors for enantiomeric detection in solution [Internet]. Dyes and Pigments. 2019 ; 165 372-382.[citado 2024 maio 25 ] Available from: https://doi.org/10.1016/j.dyepig.2019.02.047
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
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
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: 25 maio 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 maio 25 ] 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 maio 25 ] Available from: https://doi.org/10.1016/j.tet.2019.02.001
Artigo de periodico
Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles (2019)
Balfour, Michael N; Schpector, Júlio Zukerman; Rodriguez, Maria Jose Davila; Reis, Joel Savi dos; Esteves, Carlos Henrique Alves; Stefani, Hélio Alexandre
Source: Synthetic Communications. Unidade: FCF
Subjects: COMPOSTOS HETEROCÍCLICOS, SÍNTESE QUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BALFOUR, Michael N et al. Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles. Synthetic Communications, v. 49, n. 3, p. 351-358, 2019Tradução . . Disponível em: https://doi.org/10.1080/00397911.2018.1545032. Acesso em: 25 maio 2024.
APA
Balfour, M. N., Schpector, J. Z., Rodriguez, M. J. D., Reis, J. S. dos, Esteves, C. H. A., & Stefani, H. A. (2019). Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles. Synthetic Communications, 49( 3), 351-358. doi:10.1080/00397911.2018.1545032
NLM
Balfour MN, Schpector JZ, Rodriguez MJD, Reis JS dos, Esteves CHA, Stefani HA. Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles [Internet]. Synthetic Communications. 2019 ; 49( 3): 351-358.[citado 2024 maio 25 ] Available from: https://doi.org/10.1080/00397911.2018.1545032
Vancouver
Balfour MN, Schpector JZ, Rodriguez MJD, Reis JS dos, Esteves CHA, Stefani HA. Combination of Sonogashira coupling and 5-endo-dig cyclization for the synthesis of 2,6-disubstituted-5-azaindoles [Internet]. Synthetic Communications. 2019 ; 49( 3): 351-358.[citado 2024 maio 25 ] Available from: https://doi.org/10.1080/00397911.2018.1545032

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