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Artigo de periodico
Differential specificity of SARS-CoV-2 main protease variants on peptide versus protein-based substrates (2024)
Rocho, Fernanda dos Reis ; Snipas, Scott J.; Shamim, Anwar ; Rut, Wioletta; Drag, Marcin; Montanari, Carlos Alberto
Source: The FEBS Journal. Unidade: IQSC
Subjects: COVID-19, PEPTÍDEOS, PROTEÍNAS
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ABNT
ROCHO, Fernanda dos Reis et al. Differential specificity of SARS-CoV-2 main protease variants on peptide versus protein-based substrates. The FEBS Journal, v. 291, n. 1, p. 61–69, 2024Tradução . . Disponível em: https://doi.org/10.1111/febs.16970. Acesso em: 02 dez. 2025.
APA
Rocho, F. dos R., Snipas, S. J., Shamim, A., Rut, W., Drag, M., & Montanari, C. A. (2024). Differential specificity of SARS-CoV-2 main protease variants on peptide versus protein-based substrates. The FEBS Journal, 291( 1), 61–69. doi:10.1111/febs.16970
NLM
Rocho F dos R, Snipas SJ, Shamim A, Rut W, Drag M, Montanari CA. Differential specificity of SARS-CoV-2 main protease variants on peptide versus protein-based substrates [Internet]. The FEBS Journal. 2024 ; 291( 1): 61–69.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1111/febs.16970
Vancouver
Rocho F dos R, Snipas SJ, Shamim A, Rut W, Drag M, Montanari CA. Differential specificity of SARS-CoV-2 main protease variants on peptide versus protein-based substrates [Internet]. The FEBS Journal. 2024 ; 291( 1): 61–69.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1111/febs.16970
Artigo de periodico
Leaf tissue metabolomics fingerprinting of Citronella gongonha Mart. by 1H HR-MAS NMR (2022)
Ali, Sher ; Badshah, Gul; Ali, Umar; Afridi, Muhammad Siddique; Shamim, Anwar ; Khan, Ajmir ; Soares, Frederico Luiz Felipe; Menezes, Leociley Rocha Alencar; Rezende, Vanessa Theodoro ; Barison, Andersson ; Oliveira, Carlos Augusto Fernandes de ; Tonin, Fernando Gustavo
Source: Scientific Reports. Unidades: FZEA, IQSC, FMVZ
Subjects: DATILOSCOPIA, METABOLÔMICA, RESSONÂNCIA MAGNÉTICA NUCLEAR
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ABNT
ALI, Sher et al. Leaf tissue metabolomics fingerprinting of Citronella gongonha Mart. by 1H HR-MAS NMR. Scientific Reports, v. 12, p. 17624, 2022Tradução . . Disponível em: https://doi.org/10.1038/s41598-022-22708-w. Acesso em: 02 dez. 2025.
APA
Ali, S., Badshah, G., Ali, U., Afridi, M. S., Shamim, A., Khan, A., et al. (2022). Leaf tissue metabolomics fingerprinting of Citronella gongonha Mart. by 1H HR-MAS NMR. Scientific Reports, 12, 17624. doi:10.1038/s41598-022-22708-w
NLM
Ali S, Badshah G, Ali U, Afridi MS, Shamim A, Khan A, Soares FLF, Menezes LRA, Rezende VT, Barison A, Oliveira CAF de, Tonin FG. Leaf tissue metabolomics fingerprinting of Citronella gongonha Mart. by 1H HR-MAS NMR [Internet]. Scientific Reports. 2022 ;12 17624.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1038/s41598-022-22708-w
Vancouver
Ali S, Badshah G, Ali U, Afridi MS, Shamim A, Khan A, Soares FLF, Menezes LRA, Rezende VT, Barison A, Oliveira CAF de, Tonin FG. Leaf tissue metabolomics fingerprinting of Citronella gongonha Mart. by 1H HR-MAS NMR [Internet]. Scientific Reports. 2022 ;12 17624.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1038/s41598-022-22708-w
Artigo de periodico
Synthesis, biochemical evaluation and molecular modeling studies of nonpeptidic nitrile-based fluorinated compounds (2021)
Lameiro, Rafael da Fonseca; Shamim, Anwar ; Rosini, Fabiana; Cendron, Rodrigo; Batista, Pedro Henrique Jatai ; Montanari, Carlos Alberto
Source: Future Medicinal Chemistry. Unidade: IQSC
Subjects: DOENÇA DE CHAGAS, LEISHMANIA MEXICANA
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ABNT
LAMEIRO, Rafael da Fonseca et al. Synthesis, biochemical evaluation and molecular modeling studies of nonpeptidic nitrile-based fluorinated compounds. Future Medicinal Chemistry, v. 13, n. 1, p. 25–43, 2021Tradução . . Disponível em: https://doi.org/10.4155/fmc-2020-0057. Acesso em: 02 dez. 2025.
APA
Lameiro, R. da F., Shamim, A., Rosini, F., Cendron, R., Batista, P. H. J., & Montanari, C. A. (2021). Synthesis, biochemical evaluation and molecular modeling studies of nonpeptidic nitrile-based fluorinated compounds. Future Medicinal Chemistry, 13( 1), 25–43. doi:10.4155/fmc-2020-0057
NLM
Lameiro R da F, Shamim A, Rosini F, Cendron R, Batista PHJ, Montanari CA. Synthesis, biochemical evaluation and molecular modeling studies of nonpeptidic nitrile-based fluorinated compounds [Internet]. Future Medicinal Chemistry. 2021 ; 13( 1): 25–43.[citado 2025 dez. 02 ] Available from: https://doi.org/10.4155/fmc-2020-0057
Vancouver
Lameiro R da F, Shamim A, Rosini F, Cendron R, Batista PHJ, Montanari CA. Synthesis, biochemical evaluation and molecular modeling studies of nonpeptidic nitrile-based fluorinated compounds [Internet]. Future Medicinal Chemistry. 2021 ; 13( 1): 25–43.[citado 2025 dez. 02 ] Available from: https://doi.org/10.4155/fmc-2020-0057
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: 02 dez. 2025.
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 2025 dez. 02 ] 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 2025 dez. 02 ] Available from: https://doi.org/10.1016/j.bioorg.2021.104709
Artigo de periodico
Design, synthesis and stepwise optimization of nitrile-based inhibitors of cathepsins B and L (2021)
Cianni, Lorenzo ; Rocho, Fernanda dos Reis ; Bonatto, Vinícius ; Martins, Felipe Cardoso Prado ; Lameira, Jerônimo ; Leitão, Andrei ; Montanari, Carlos Alberto ; Shamim, Anwar
Source: Bioorganic and Medicinal Chemistry. Unidade: IQSC
Subjects: QUÍMICA MÉDICA, NEOPLASIAS, INIBIDORES DE ENZIMAS
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ABNT
CIANNI, Lorenzo et al. Design, synthesis and stepwise optimization of nitrile-based inhibitors of cathepsins B and L. Bioorganic and Medicinal Chemistry, v. 29, p. 115827, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.bmc.2020.115827. Acesso em: 02 dez. 2025.
APA
Cianni, L., Rocho, F. dos R., Bonatto, V., Martins, F. C. P., Lameira, J., Leitão, A., et al. (2021). Design, synthesis and stepwise optimization of nitrile-based inhibitors of cathepsins B and L. Bioorganic and Medicinal Chemistry, 29, 115827. doi:10.1016/j.bmc.2020.115827
NLM
Cianni L, Rocho F dos R, Bonatto V, Martins FCP, Lameira J, Leitão A, Montanari CA, Shamim A. Design, synthesis and stepwise optimization of nitrile-based inhibitors of cathepsins B and L [Internet]. Bioorganic and Medicinal Chemistry. 2021 ; 29 115827.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1016/j.bmc.2020.115827
Vancouver
Cianni L, Rocho F dos R, Bonatto V, Martins FCP, Lameira J, Leitão A, Montanari CA, Shamim A. Design, synthesis and stepwise optimization of nitrile-based inhibitors of cathepsins B and L [Internet]. Bioorganic and Medicinal Chemistry. 2021 ; 29 115827.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1016/j.bmc.2020.115827
Artigo de periodico
Predicting the Relative Binding Affinity for Reversible Covalent Inhibitors by Free Energy Perturbation Calculations (2021)
Bonatto, Vinícius ; Shamim, Anwar ; Rocho, Fernanda dos Reis ; Leitão, Andrei ; Luque, F. Javier; Montanari, Carlos Alberto
Source: Journal of Chemical Information and Modeling. Unidade: IQSC
Subjects: MEDICAMENTO, ENZIMAS
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ABNT
BONATTO, Vinícius et al. Predicting the Relative Binding Affinity for Reversible Covalent Inhibitors by Free Energy Perturbation Calculations. Journal of Chemical Information and Modeling, v. 61, p. 4733−4744, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.jcim.1c00515. Acesso em: 02 dez. 2025.
APA
Bonatto, V., Shamim, A., Rocho, F. dos R., Leitão, A., Luque, F. J., & Montanari, C. A. (2021). Predicting the Relative Binding Affinity for Reversible Covalent Inhibitors by Free Energy Perturbation Calculations. Journal of Chemical Information and Modeling, 61, 4733−4744. doi:10.1021/acs.jcim.1c00515
NLM
Bonatto V, Shamim A, Rocho F dos R, Leitão A, Luque FJ, Montanari CA. Predicting the Relative Binding Affinity for Reversible Covalent Inhibitors by Free Energy Perturbation Calculations [Internet]. Journal of Chemical Information and Modeling. 2021 ; 61 4733−4744.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.jcim.1c00515
Vancouver
Bonatto V, Shamim A, Rocho F dos R, Leitão A, Luque FJ, Montanari CA. Predicting the Relative Binding Affinity for Reversible Covalent Inhibitors by Free Energy Perturbation Calculations [Internet]. Journal of Chemical Information and Modeling. 2021 ; 61 4733−4744.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.jcim.1c00515
Artigo de periodico
Dipeptidyl nitrile derivatives suppress the Trypanosoma cruzi in vitro infection (2020)
Quilles Junior, José Carlos ; Shamim, Anwar ; Tezuka, Daiane Yukie; Batista, Pedro Henrique Jatai ; Lopes, Carla Duque ; Albuquerque, Sérgio de ; Montanari, Carlos Alberto ; Leitão, Andrei
Source: Experimental Parasitology. Unidades: FCFRP, IQSC, Interunidades em Bioengenharia, EESC
Assunto: DOENÇA DE CHAGAS
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ABNT
QUILLES JUNIOR, José Carlos et al. Dipeptidyl nitrile derivatives suppress the Trypanosoma cruzi in vitro infection. Experimental Parasitology, v. 219, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.exppara.2020.108032. Acesso em: 02 dez. 2025.
APA
Quilles Junior, J. C., Shamim, A., Tezuka, D. Y., Batista, P. H. J., Lopes, C. D., Albuquerque, S. de, et al. (2020). Dipeptidyl nitrile derivatives suppress the Trypanosoma cruzi in vitro infection. Experimental Parasitology, 219. doi:10.1016/j.exppara.2020.108032
NLM
Quilles Junior JC, Shamim A, Tezuka DY, Batista PHJ, Lopes CD, Albuquerque S de, Montanari CA, Leitão A. Dipeptidyl nitrile derivatives suppress the Trypanosoma cruzi in vitro infection [Internet]. Experimental Parasitology. 2020 ; 219[citado 2025 dez. 02 ] Available from: https://doi.org/10.1016/j.exppara.2020.108032
Vancouver
Quilles Junior JC, Shamim A, Tezuka DY, Batista PHJ, Lopes CD, Albuquerque S de, Montanari CA, Leitão A. Dipeptidyl nitrile derivatives suppress the Trypanosoma cruzi in vitro infection [Internet]. Experimental Parasitology. 2020 ; 219[citado 2025 dez. 02 ] Available from: https://doi.org/10.1016/j.exppara.2020.108032
Artigo de periodico
Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteases (2020)
Cianni, Lorenzo ; Rocho, Fernanda dos Reis ; Rosini, Fabiana; Bonatto, Vinícius ; Ribeiro, Jean Francisco Rosa ; Lameira, Jerônimo ; Leitão, Andrei ; Shamim, Anwar ; Montanari, Carlos Alberto
Source: Bioorganic Chemistry. Unidade: IQSC
Subjects: FÁRMACOS, BIOMARCADORES, PROTEÍNAS
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ABNT
CIANNI, Lorenzo et al. Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteases. Bioorganic Chemistry, v. 101, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bioorg.2020.104039. Acesso em: 02 dez. 2025.
APA
Cianni, L., Rocho, F. dos R., Rosini, F., Bonatto, V., Ribeiro, J. F. R., Lameira, J., et al. (2020). Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteases. Bioorganic Chemistry, 101. doi:10.1016/j.bioorg.2020.104039
NLM
Cianni L, Rocho F dos R, Rosini F, Bonatto V, Ribeiro JFR, Lameira J, Leitão A, Shamim A, Montanari CA. Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteases [Internet]. Bioorganic Chemistry. 2020 ; 101[citado 2025 dez. 02 ] Available from: https://doi.org/10.1016/j.bioorg.2020.104039
Vancouver
Cianni L, Rocho F dos R, Rosini F, Bonatto V, Ribeiro JFR, Lameira J, Leitão A, Shamim A, Montanari CA. Optimization strategy of single-digit nanomolar cross-class inhibitors of mammalian and protozoa cysteine proteases [Internet]. Bioorganic Chemistry. 2020 ; 101[citado 2025 dez. 02 ] Available from: https://doi.org/10.1016/j.bioorg.2020.104039
Trabalho de evento-resumo
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: 02 dez. 2025.
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 2025 dez. 02 ] 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 2025 dez. 02 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Artigo de periodico
Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones (2019)
Vasconcelos, Stanley Nunes Siqueira ; Oliveira, Isadora Maria de ; Shamim, Anwar ; Zukerman-Schpector, Júlio ; Pimenta, Daniel Carvalho ; Stefani, Hélio Alexandre
Source: Advanced Synthesis & Catalysis. Unidades: FCF, IQSC
Subjects: ALDEÍDOS, ESTEREOQUÍMICA
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ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones. Advanced Synthesis & Catalysis, v. 361, p. 4243-4254, 2019Tradução . . Disponível em: https://doi.org/10.1002/adsc.201900564. Acesso em: 02 dez. 2025.
APA
Vasconcelos, S. N. S., Oliveira, I. M. de, Shamim, A., Zukerman-Schpector, J., Pimenta, D. C., & Stefani, H. A. (2019). Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones. Advanced Synthesis & Catalysis, 361, 4243-4254. doi:10.1002/adsc.201900564
NLM
Vasconcelos SNS, Oliveira IM de, Shamim A, Zukerman-Schpector J, Pimenta DC, Stefani HA. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones [Internet]. Advanced Synthesis & Catalysis. 2019 ; 361 4243-4254.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1002/adsc.201900564
Vancouver
Vasconcelos SNS, Oliveira IM de, Shamim A, Zukerman-Schpector J, Pimenta DC, Stefani HA. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones [Internet]. Advanced Synthesis & Catalysis. 2019 ; 361 4243-4254.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1002/adsc.201900564
Trabalho de evento-resumo
Synthesis of Dipeptidyl and Peptidomimetic Nitriles as Cruzain, CPB and Related Human Cathepsins Inhibitors (2019)
Shamim, Anwar ; Montanari, Carlos Alberto
Source: Book of Abstracts. Conference titles: The São Carlos Special Medicinal Chemistry Meeting - SancaMedChem2019. Unidade: IQSC
Assunto: QUÍMICA MÉDICA
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ABNT
SHAMIM, Anwar e MONTANARI, Carlos Alberto. Synthesis of Dipeptidyl and Peptidomimetic Nitriles as Cruzain, CPB and Related Human Cathepsins Inhibitors. 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: 02 dez. 2025.
APA
Shamim, A., & Montanari, C. A. (2019). Synthesis of Dipeptidyl and Peptidomimetic Nitriles as Cruzain, CPB and Related Human Cathepsins Inhibitors. 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
Shamim A, Montanari CA. Synthesis of Dipeptidyl and Peptidomimetic Nitriles as Cruzain, CPB and Related Human Cathepsins Inhibitors [Internet]. Book of Abstracts. 2019 ;[citado 2025 dez. 02 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Vancouver
Shamim A, Montanari CA. Synthesis of Dipeptidyl and Peptidomimetic Nitriles as Cruzain, CPB and Related Human Cathepsins Inhibitors [Internet]. Book of Abstracts. 2019 ;[citado 2025 dez. 02 ] Available from: http://sancamedchem.iqsc.usp.br/files/2019/11/Book-of-abstracts-SancaMedChem2019.pdf
Tese (Doutorado)
Funcionalização de 3,4,6-tri-O-acetil-D-glucal via click chemistry e reações de acoplamento cruzado catalizado por paládio (2017)
Shamim, Anwar; Stefani, Hélio Alexandre (Orientador)
Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, PALÁDIO
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ABNT
SHAMIM, Anwar. Funcionalização de 3,4,6-tri-O-acetil-D-glucal via click chemistry e reações de acoplamento cruzado catalizado por paládio. 2017. Tese (Doutorado) – Universidade de São Paulo, São Paulo, 2017. Disponível em: http://www.teses.usp.br/teses/disponiveis/46/46136/tde-22112017-143637/. Acesso em: 02 dez. 2025.
APA
Shamim, A. (2017). Funcionalização de 3,4,6-tri-O-acetil-D-glucal via click chemistry e reações de acoplamento cruzado catalizado por paládio (Tese (Doutorado). Universidade de São Paulo, São Paulo. Recuperado de http://www.teses.usp.br/teses/disponiveis/46/46136/tde-22112017-143637/
NLM
Shamim A. Funcionalização de 3,4,6-tri-O-acetil-D-glucal via click chemistry e reações de acoplamento cruzado catalizado por paládio [Internet]. 2017 ;[citado 2025 dez. 02 ] Available from: http://www.teses.usp.br/teses/disponiveis/46/46136/tde-22112017-143637/
Vancouver
Shamim A. Funcionalização de 3,4,6-tri-O-acetil-D-glucal via click chemistry e reações de acoplamento cruzado catalizado por paládio [Internet]. 2017 ;[citado 2025 dez. 02 ] Available from: http://www.teses.usp.br/teses/disponiveis/46/46136/tde-22112017-143637/

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