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2,2,2-Trifluoroethylamine as a peptidic bond bioisostere in reversible covalent inhibitors of cysteine proteases (2019)
Lameiro, Rafael da Fonseca; Shamim, Anwar ; Montanari, Carlos Alberto
Source: Book of Abstracts. Conference titles: The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem2019. Unidade: IQSC
Subjects: SÍNTESE ORGÂNICA, DOENÇAS PARASITÁRIAS, PEPTÍDEOS
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ABNT
LAMEIRO, Rafael da Fonseca e SHAMIM, Anwar e MONTANARI, Carlos Alberto. 2,2,2-Trifluoroethylamine as a peptidic bond bioisostere in reversible covalent inhibitors of cysteine proteases. 2019, Anais.. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP, 2019. Disponível em: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf. Acesso em: 24 ago. 2024.
APA
Lameiro, R. da F., Shamim, A., & Montanari, C. A. (2019). 2,2,2-Trifluoroethylamine as a peptidic bond bioisostere in reversible covalent inhibitors of cysteine proteases. In Book of Abstracts. São Paulo: Instituto de Química de São Carlos, IQSC, Universidade de São Paulo, USP. Recuperado de http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
NLM
Lameiro R da F, Shamim A, Montanari CA. 2,2,2-Trifluoroethylamine as a peptidic bond bioisostere in reversible covalent inhibitors of cysteine proteases [Internet]. Book of Abstracts. 2019 ;[citado 2024 ago. 24 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Vancouver
Lameiro R da F, Shamim A, Montanari CA. 2,2,2-Trifluoroethylamine as a peptidic bond bioisostere in reversible covalent inhibitors of cysteine proteases [Internet]. Book of Abstracts. 2019 ;[citado 2024 ago. 24 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Artigo de periodico
Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives (2017)
Shamim, Anwar; Vasconcelos, Stanley Nunes Siqueira; Oliveira, Isadora Maria de; Reis, Joel Savi dos; Pimenta, Daniel Carvalho; Zukerman-Schpector, Júlio; Stefani, Hélio Alexandre
Source: Synthesis. Unidade: FCF
Assunto: SÍNTESE ORGÂNICA
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ABNT
SHAMIM, Anwar et al. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, v. 49, n. 23, p. 5183-5196, 2017Tradução . . Disponível em: https://doi.org/10.1055/s-0036-1589090. Acesso em: 24 ago. 2024.
APA
Shamim, A., Vasconcelos, S. N. S., Oliveira, I. M. de, Reis, J. S. dos, Pimenta, D. C., Zukerman-Schpector, J., & Stefani, H. A. (2017). Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives. Synthesis, 49( 23), 5183-5196. doi:10.1055/s-0036-1589090
NLM
Shamim A, Vasconcelos SNS, Oliveira IM de, Reis JS dos, Pimenta DC, Zukerman-Schpector J, Stefani HA. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives [Internet]. Synthesis. 2017 ; 49( 23): 5183-5196.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1055/s-0036-1589090
Vancouver
Shamim A, Vasconcelos SNS, Oliveira IM de, Reis JS dos, Pimenta DC, Zukerman-Schpector J, Stefani HA. Synthesis of glycosyl azides and their applications using CuAAC click chemistry to generate bis- and tris(triazolyl)glycosyl derivatives [Internet]. Synthesis. 2017 ; 49( 23): 5183-5196.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1055/s-0036-1589090
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
Source: Tetrahedron Letters. Unidade: FCF
Subjects: 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: 24 ago. 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 ago. 24 ] 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 ago. 24 ] Available from: https://doi.org/10.1016/j.tetlet.2017.01.059
Artigo de periodico
Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles (2017)
Ali, Bakhat; Vasconcelos, Stanley N. S; Shamim, Anwar; Schpector, Júlio Zukerman; Stefani, Hélio Alexandre
Source: Arabian Journal of Chemistry. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, REAÇÕES QUÍMICAS
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ABNT
ALI, Bakhat et al. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles. Arabian Journal of Chemistry, v. 10, n. 4, p. 500-508, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.arabjc.2016.06.003. Acesso em: 24 ago. 2024.
APA
Ali, B., Vasconcelos, S. N. S., Shamim, A., Schpector, J. Z., & Stefani, H. A. (2017). Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles. Arabian Journal of Chemistry, 10( 4), 500-508. doi:10.1016/j.arabjc.2016.06.003
NLM
Ali B, Vasconcelos SNS, Shamim A, Schpector JZ, Stefani HA. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles [Internet]. Arabian Journal of Chemistry. 2017 ; 10( 4): 500-508.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.arabjc.2016.06.003
Vancouver
Ali B, Vasconcelos SNS, Shamim A, Schpector JZ, Stefani HA. Synthesis of 1-((4-methoxyphenyl)-3-alkynes)-1H-pyrrole-2,5-diones and functionalization to triazoles [Internet]. Arabian Journal of Chemistry. 2017 ; 10( 4): 500-508.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1016/j.arabjc.2016.06.003
Artigo de periodico
3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions (2017)
Vasconcelos, Stanley N. S; Silva, Vitor Hugo Menezes da; Braga, Ataualpa Albert Carmo ; Shamim, Anwar; Souza, Frederico B; Pimenta, Daniel C; Stefani, Hélio Alexandre
Source: Asian Journal Organic of Chemistry. Unidades: IQ, FCF
Subjects: SÍNTESE ORGÂNICA, COMPOSTOS ORGÂNICOS
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ABNT
VASCONCELOS, Stanley N. S et al. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Asian Journal Organic of Chemistry, v. 6, n. 7, p. 913-920, 2017Tradução . . Disponível em: https://doi.org/10.1002/ajoc.201700154. Acesso em: 24 ago. 2024.
APA
Vasconcelos, S. N. S., Silva, V. H. M. da, Braga, A. A. C., Shamim, A., Souza, F. B., Pimenta, D. C., & Stefani, H. A. (2017). 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions. Asian Journal Organic of Chemistry, 6( 7), 913-920. doi:10.1002/ajoc.201700154
NLM
Vasconcelos SNS, Silva VHM da, Braga AAC, Shamim A, Souza FB, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions [Internet]. Asian Journal Organic of Chemistry. 2017 ; 6( 7): 913-920.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1002/ajoc.201700154
Vancouver
Vasconcelos SNS, Silva VHM da, Braga AAC, Shamim A, Souza FB, Pimenta DC, Stefani HA. 3-Alkenyltyrosines accessed by suzukim Miyaura coupling: a key Intermediate in the synthesis and mechanistic study of povarov multicomponent reactions [Internet]. Asian Journal Organic of Chemistry. 2017 ; 6( 7): 913-920.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1002/ajoc.201700154
Artigo de periodico
Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines (2017)
Oliveira, Isadora M. de; Vasconcelos, Stanley S. N; Barbeiro, Cristiane S; Correra, Thiago Carita ; Shamim, Anwar; Pimenta, Daniel Carvalho; Caracelli, Ignez; Schpector, Júlio Zukerman; Stefani, Hélio Alexandre ; Manarin, Flávia
Source: New Journal of Chemistry. Unidades: IQ, FCF
Subjects: SÍNTESE ORGÂNICA, REAÇÕES ORGÂNICAS
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ABNT
OLIVEIRA, Isadora M. de et al. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines. New Journal of Chemistry, v. 41, p. 9884-9888, 2017Tradução . . Disponível em: https://doi.org/10.1039/c7nj01803g. Acesso em: 24 ago. 2024.
APA
Oliveira, I. M. de, Vasconcelos, S. S. N., Barbeiro, C. S., Correra, T. C., Shamim, A., Pimenta, D. C., et al. (2017). Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines. New Journal of Chemistry, 41, 9884-9888. doi:10.1039/c7nj01803g
NLM
Oliveira IM de, Vasconcelos SSN, Barbeiro CS, Correra TC, Shamim A, Pimenta DC, Caracelli I, Schpector JZ, Stefani HA, Manarin F. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines [Internet]. New Journal of Chemistry. 2017 ; 41 9884-9888.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1039/c7nj01803g
Vancouver
Oliveira IM de, Vasconcelos SSN, Barbeiro CS, Correra TC, Shamim A, Pimenta DC, Caracelli I, Schpector JZ, Stefani HA, Manarin F. Ytterbium(III)-catalyzed three-component reactions: synthesis of 4-organoselenium-quinolines [Internet]. New Journal of Chemistry. 2017 ; 41 9884-9888.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1039/c7nj01803g
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
Source: 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: 24 ago. 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 ago. 24 ] 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 ago. 24 ] Available from: https://doi.org/10.1016/j.tetlet.2015.05.066
Artigo de periodico
Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement (2015)
Souza, Frederico B; Shamim, Anwar; Argomedo, Luiz M. Z; Pimenta, Daniel Carvalho; Stefani, Hélio Alexandre
Source: Molecular Diversity. Unidade: FCF
Subjects: SÍNTESE ORGÂNICA, REAGENTES ORGÂNICOS
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ABNT
SOUZA, Frederico B et al. Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement. Molecular Diversity, v. 19, n. 4, p. 773-785, 2015Tradução . . Disponível em: https://doi.org/10.1007/s11030-015-9619-x. Acesso em: 24 ago. 2024.
APA
Souza, F. B., Shamim, A., Argomedo, L. M. Z., Pimenta, D. C., & Stefani, H. A. (2015). Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement. Molecular Diversity, 19( 4), 773-785. doi:10.1007/s11030-015-9619-x
NLM
Souza FB, Shamim A, Argomedo LMZ, Pimenta DC, Stefani HA. Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement [Internet]. Molecular Diversity. 2015 ; 19( 4): 773-785.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s11030-015-9619-x
Vancouver
Souza FB, Shamim A, Argomedo LMZ, Pimenta DC, Stefani HA. Synthesis of enyne and aryl vinyl sulfoxides: functionalization via Pummerer rearrangement [Internet]. Molecular Diversity. 2015 ; 19( 4): 773-785.[citado 2024 ago. 24 ] Available from: https://doi.org/10.1007/s11030-015-9619-x

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