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Artigo de periodico
Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones (2021)
Day, David P; Vargas, Jorge A. M.; Burtoloso, Antonio Carlos Bender
Fonte: The Chemical Record. Unidade: IQSC
Assuntos: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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ABNT
DAY, David P e VARGAS, Jorge A. M. e BURTOLOSO, Antonio Carlos Bender. Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones. The Chemical Record, v. 21, p. 1-19, 2021Tradução . . Disponível em: https://doi.org/10.1002/tcr.20200017. Acesso em: 05 dez. 2025.
APA
Day, D. P., Vargas, J. A. M., & Burtoloso, A. C. B. (2021). Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones. The Chemical Record, 21, 1-19. doi:10.1002/tcr.20200017
NLM
Day DP, Vargas JAM, Burtoloso ACB. Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones [Internet]. The Chemical Record. 2021 ;21 1-19.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1002/tcr.20200017
Vancouver
Day DP, Vargas JAM, Burtoloso ACB. Synthetic Routes Towards the Synthesis of Geminal α-Difunctionalized Ketones [Internet]. The Chemical Record. 2021 ;21 1-19.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1002/tcr.20200017
Artigo de periodico
Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network (2021)
Khalid, Muhammad ; Ali, Akbar ; Khan, Muhammad Usman ; Tahir, Muhammad Nawaz; Ahmad, Anees ; Ashfaq, Muhammad; Hussain, Riaz; Morais, Sara Figueirêdo de Alcântara ; Braga, Ataualpa Albert Carmo
Fonte: Journal of Molecular Structure. Unidades: IQ, IQSC
Assuntos: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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ABNT
KHALID, Muhammad et al. Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network. Journal of Molecular Structure, v. 1230 p. 129827, 2021Tradução . . Disponível em: https://doi.org/10.1016/j.molstruc.2020.129827. Acesso em: 05 dez. 2025.
APA
Khalid, M., Ali, A., Khan, M. U., Tahir, M. N., Ahmad, A., Ashfaq, M., et al. (2021). Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network. Journal of Molecular Structure, 1230 p. 129827. doi:10.1016/j.molstruc.2020.129827
NLM
Khalid M, Ali A, Khan MU, Tahir MN, Ahmad A, Ashfaq M, Hussain R, Morais SF de A, Braga AAC. Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network [Internet]. Journal of Molecular Structure. 2021 ; 1230 p. 129827[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129827
Vancouver
Khalid M, Ali A, Khan MU, Tahir MN, Ahmad A, Ashfaq M, Hussain R, Morais SF de A, Braga AAC. Non-covalent interactions abetted supramolecular arrangements of N -Substitute d b enzylidene acetohydrazide to direct its solid-state network [Internet]. Journal of Molecular Structure. 2021 ; 1230 p. 129827[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.molstruc.2020.129827
Artigo de periodico
Cross-Linked and surface-modified cellulose acetate as a cover layer for paper-based electrochromic devices (2021)
Kaschuk, Joice Jaqueline ; Borghei, Maryam; Solin, Katariina; Tripathi, Anurodh; Khakalo, Alexey ; Leite, Fábio A. S.; Branco, Aida; Sousa, Miriam C. Amores de; Frollini, Elisabete ; Rojas, Orlando Jose
Fonte: ACS Applied Polymer Materials. Unidade: IQSC
Assuntos: QUÍMICA ORGÂNICA, CELULOSE, BIODEGRADAÇÃO AMBIENTAL
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KASCHUK, Joice Jaqueline et al. Cross-Linked and surface-modified cellulose acetate as a cover layer for paper-based electrochromic devices. ACS Applied Polymer Materials, v. 3, n. 5, p. 2393–2401, 2021Tradução . . Disponível em: https://doi.org/10.1021/acsapm.0c01252. Acesso em: 05 dez. 2025.
APA
Kaschuk, J. J., Borghei, M., Solin, K., Tripathi, A., Khakalo, A., Leite, F. A. S., et al. (2021). Cross-Linked and surface-modified cellulose acetate as a cover layer for paper-based electrochromic devices. ACS Applied Polymer Materials, 3( 5), 2393–2401. doi:10.1021/acsapm.0c01252
NLM
Kaschuk JJ, Borghei M, Solin K, Tripathi A, Khakalo A, Leite FAS, Branco A, Sousa MCA de, Frollini E, Rojas OJ. Cross-Linked and surface-modified cellulose acetate as a cover layer for paper-based electrochromic devices [Internet]. ACS Applied Polymer Materials. 2021 ; 3( 5): 2393–2401.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/acsapm.0c01252
Vancouver
Kaschuk JJ, Borghei M, Solin K, Tripathi A, Khakalo A, Leite FAS, Branco A, Sousa MCA de, Frollini E, Rojas OJ. Cross-Linked and surface-modified cellulose acetate as a cover layer for paper-based electrochromic devices [Internet]. ACS Applied Polymer Materials. 2021 ; 3( 5): 2393–2401.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/acsapm.0c01252
Artigo de periodico
Phytotoxic Tryptoquialanines Produced In Vivo by Penicillium digitatum Are Exported in Extracellular Vesicles (2021)
Costa, Jonas Henrique ; Bazioli, Jaqueline Moraes; Barbosa, Luidy Darllan; Santos Júnior, Pedro Luis Theodoro dos; Reis, Flavia C. G.; Klimeck, Tabata; Crnkovic, Camila Manoel ; Berlinck, Roberto Gomes de Souza ; Sussulini, Alessandra; Rodrigues, Márcio Lourenço ; Fill, Taicia Pacheco
Fonte: mBio. Unidades: IQSC, FCF
Assuntos: QUÍMICA ORGÂNICA, FITOPATÓGENOS, FUNGOS, MOFO VERDE
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ABNT
COSTA, Jonas Henrique et al. Phytotoxic Tryptoquialanines Produced In Vivo by Penicillium digitatum Are Exported in Extracellular Vesicles. mBio, v. 12, n. 1, 2021Tradução . . Disponível em: https://doi.org/10.1128/mBio.03393-20. Acesso em: 05 dez. 2025.
APA
Costa, J. H., Bazioli, J. M., Barbosa, L. D., Santos Júnior, P. L. T. dos, Reis, F. C. G., Klimeck, T., et al. (2021). Phytotoxic Tryptoquialanines Produced In Vivo by Penicillium digitatum Are Exported in Extracellular Vesicles. mBio, 12( 1). doi:10.1128/mBio.03393-20
NLM
Costa JH, Bazioli JM, Barbosa LD, Santos Júnior PLT dos, Reis FCG, Klimeck T, Crnkovic CM, Berlinck RG de S, Sussulini A, Rodrigues ML, Fill TP. Phytotoxic Tryptoquialanines Produced In Vivo by Penicillium digitatum Are Exported in Extracellular Vesicles [Internet]. mBio. 2021 ; 12( 1):[citado 2025 dez. 05 ] Available from: https://doi.org/10.1128/mBio.03393-20
Vancouver
Costa JH, Bazioli JM, Barbosa LD, Santos Júnior PLT dos, Reis FCG, Klimeck T, Crnkovic CM, Berlinck RG de S, Sussulini A, Rodrigues ML, Fill TP. Phytotoxic Tryptoquialanines Produced In Vivo by Penicillium digitatum Are Exported in Extracellular Vesicles [Internet]. mBio. 2021 ; 12( 1):[citado 2025 dez. 05 ] Available from: https://doi.org/10.1128/mBio.03393-20
Artigo de periodico
Substituted Naphthols: Preparations, Applications, and Reactions (2021)
Vargas,Jorge Andrés Mora; Day, David P; Burtoloso, Antonio Carlos Bender
Fonte: European Journal of Organic Chemistry. Unidade: IQSC
Assuntos: QUÍMICA ORGÂNICA, PRODUTOS NATURAIS
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ABNT
VARGAS, Jorge Andrés Mora e DAY, David P e BURTOLOSO, Antonio Carlos Bender. Substituted Naphthols: Preparations, Applications, and Reactions. European Journal of Organic Chemistry, v. press, 2021Tradução . . Disponível em: https://doi.org/10.1002/ejoc.202001132. Acesso em: 05 dez. 2025.
APA
Vargas, J. A. M., Day, D. P., & Burtoloso, A. C. B. (2021). Substituted Naphthols: Preparations, Applications, and Reactions. European Journal of Organic Chemistry, press. doi:10.1002/ejoc.202001132
NLM
Vargas JAM, Day DP, Burtoloso ACB. Substituted Naphthols: Preparations, Applications, and Reactions [Internet]. European Journal of Organic Chemistry. 2021 ; press[citado 2025 dez. 05 ] Available from: https://doi.org/10.1002/ejoc.202001132
Vancouver
Vargas JAM, Day DP, Burtoloso ACB. Substituted Naphthols: Preparations, Applications, and Reactions [Internet]. European Journal of Organic Chemistry. 2021 ; press[citado 2025 dez. 05 ] Available from: https://doi.org/10.1002/ejoc.202001132
Artigo de periodico
New tetrodotoxin analogs in Brazilian pufferfishes tissues and microbiome (2020)
Tonon, Luciane Alessandra Chimetto ; Azevedo, Gustavo Pitta Reis de; Monteiro, Afif Felix ; Bernardi,Darlon Irineu ; Gubiani, Juliana Regina ; Ióca, Laura Pavan ; Mattsson, Hannah K ; Moreira, Ana Paula Barbosa; Gomes, Alexandre F; Pires Júnior, Osmindo Rodrigues ; Pedrosa, Carolina da Silva Gouveia; Souza, Leticia R.Q.; Rehen, Stevens Kastrup; Thompson, Cristiane Carneiro; Thompson, Fabiano Lopes; Berlinck, Roberto Gomes de Souza
Fonte: Chemosphere. Unidade: IQSC
Assuntos: QUÍMICA ORGÂNICA, BACTÉRIAS, PEIXES
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ABNT
TONON, Luciane Alessandra Chimetto et al. New tetrodotoxin analogs in Brazilian pufferfishes tissues and microbiome. Chemosphere, v. 242, p. 125211, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.chemosphere.2019.125211. Acesso em: 05 dez. 2025.
APA
Tonon, L. A. C., Azevedo, G. P. R. de, Monteiro, A. F., Bernardi, D. I., Gubiani, J. R., Ióca, L. P., et al. (2020). New tetrodotoxin analogs in Brazilian pufferfishes tissues and microbiome. Chemosphere, 242, 125211. doi:10.1016/j.chemosphere.2019.125211
NLM
Tonon LAC, Azevedo GPR de, Monteiro AF, Bernardi DI, Gubiani JR, Ióca LP, Mattsson HK, Moreira APB, Gomes AF, Pires Júnior OR, Pedrosa C da SG, Souza LRQ, Rehen SK, Thompson CC, Thompson FL, Berlinck RG de S. New tetrodotoxin analogs in Brazilian pufferfishes tissues and microbiome [Internet]. Chemosphere. 2020 ; 242 125211.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.chemosphere.2019.125211
Vancouver
Tonon LAC, Azevedo GPR de, Monteiro AF, Bernardi DI, Gubiani JR, Ióca LP, Mattsson HK, Moreira APB, Gomes AF, Pires Júnior OR, Pedrosa C da SG, Souza LRQ, Rehen SK, Thompson CC, Thompson FL, Berlinck RG de S. New tetrodotoxin analogs in Brazilian pufferfishes tissues and microbiome [Internet]. Chemosphere. 2020 ; 242 125211.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.chemosphere.2019.125211
Artigo de periodico
Synthesis and matched molecular pair analysis of covalent reversible inhibitors of the cysteine protease CPB (2020)
Matos, Thiago Kelvin Brito ; Batista, Pedro Henrique Jatai ; Rocho, Fernanda dos Reis ; Vita, Daniela de ; Pearce, Nicholas; Kellam, Barrie ; Montanari, Carlos Alberto ; Leitão, Andrei
Fonte: Bioorganic & Medicinal Chemistry Letters. Unidade: IQSC
Assuntos: QUÍMICA ORGÂNICA, MEDICAMENTO, INIBIDORES DE ENZIMAS
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ABNT
MATOS, Thiago Kelvin Brito et al. Synthesis and matched molecular pair analysis of covalent reversible inhibitors of the cysteine protease CPB. Bioorganic & Medicinal Chemistry Letters, v. 30, n. 18, p. 127439, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bmcl.2020.127439. Acesso em: 05 dez. 2025.
APA
Matos, T. K. B., Batista, P. H. J., Rocho, F. dos R., Vita, D. de, Pearce, N., Kellam, B., et al. (2020). Synthesis and matched molecular pair analysis of covalent reversible inhibitors of the cysteine protease CPB. Bioorganic & Medicinal Chemistry Letters, 30( 18), 127439. doi:10.1016/j.bmcl.2020.127439
NLM
Matos TKB, Batista PHJ, Rocho F dos R, Vita D de, Pearce N, Kellam B, Montanari CA, Leitão A. Synthesis and matched molecular pair analysis of covalent reversible inhibitors of the cysteine protease CPB [Internet]. Bioorganic & Medicinal Chemistry Letters. 2020 ; 30( 18): 127439.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.bmcl.2020.127439
Vancouver
Matos TKB, Batista PHJ, Rocho F dos R, Vita D de, Pearce N, Kellam B, Montanari CA, Leitão A. Synthesis and matched molecular pair analysis of covalent reversible inhibitors of the cysteine protease CPB [Internet]. Bioorganic & Medicinal Chemistry Letters. 2020 ; 30( 18): 127439.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.bmcl.2020.127439
Artigo de periodico
Computational insights into substituent effects on the stability and reactivity of flavylium cation analogs of anthocyanins (2020)
Freitas, Adilson A; Shimizu, Karina; Dias, Luis Gustavo ; Quina, Frank Herbert
Fonte: Arkivoc. Unidades: FFCLRP, IQ
Assuntos: SAIS, QUÍMICA ORGÂNICA, CONSTANTES QUÍMICAS
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ABNT
FREITAS, Adilson A et al. Computational insights into substituent effects on the stability and reactivity of flavylium cation analogs of anthocyanins. Arkivoc, p. 146-162, 2020Tradução . . Disponível em: https://doi.org/10.24820/ark.5550190.p011.125. Acesso em: 05 dez. 2025.
APA
Freitas, A. A., Shimizu, K., Dias, L. G., & Quina, F. H. (2020). Computational insights into substituent effects on the stability and reactivity of flavylium cation analogs of anthocyanins. Arkivoc, 146-162. doi:10.24820/ark.5550190.p011.125
NLM
Freitas AA, Shimizu K, Dias LG, Quina FH. Computational insights into substituent effects on the stability and reactivity of flavylium cation analogs of anthocyanins [Internet]. Arkivoc. 2020 ; 146-162.[citado 2025 dez. 05 ] Available from: https://doi.org/10.24820/ark.5550190.p011.125
Vancouver
Freitas AA, Shimizu K, Dias LG, Quina FH. Computational insights into substituent effects on the stability and reactivity of flavylium cation analogs of anthocyanins [Internet]. Arkivoc. 2020 ; 146-162.[citado 2025 dez. 05 ] Available from: https://doi.org/10.24820/ark.5550190.p011.125
Artigo de periodico
α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles (2020)
Caiuby, Clarice Alves Dale ; Jesus, Matheus Pereira de ; Burtoloso, Antonio Carlos Bender
Fonte: The Journal of Organic Chemistry. Unidade: IQSC
Assuntos: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
CAIUBY, Clarice Alves Dale e JESUS, Matheus Pereira de e BURTOLOSO, Antonio Carlos Bender. α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles. The Journal of Organic Chemistry, v. 85, n. 11, p. 7433-7445 April 28, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.0c00833. Acesso em: 05 dez. 2025.
APA
Caiuby, C. A. D., Jesus, M. P. de, & Burtoloso, A. C. B. (2020). α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles. The Journal of Organic Chemistry, 85( 11), 7433-7445 April 28. doi:10.1021/acs.joc.0c00833
NLM
Caiuby CAD, Jesus MP de, Burtoloso ACB. α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles [Internet]. The Journal of Organic Chemistry. 2020 ;85( 11): 7433-7445 April 28.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/acs.joc.0c00833
Vancouver
Caiuby CAD, Jesus MP de, Burtoloso ACB. α‑Imino Iridium Carbenes from Imidoyl Sulfoxonium Ylides: Application in the One-Step Synthesis of Indoles [Internet]. The Journal of Organic Chemistry. 2020 ;85( 11): 7433-7445 April 28.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/acs.joc.0c00833
Artigo de periodico
Prediction of 15N NMR chemical shifts for nitrogenated aromatic compounds (2020)
Oliveira, Marcelo Tavares de; Alves, Júlia Maria Aragon; Morais, Sara Figueirêdo de Alcântara ; Braga, Ataualpa Albert Carmo
Fonte: ARKIVOC - Archive for Organic Chemistry. Unidades: IQ, IQSC
Assuntos: QUÍMICA ORGÂNICA, RESSONÂNCIA MAGNÉTICA NUCLEAR
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ABNT
OLIVEIRA, Marcelo Tavares de et al. Prediction of 15N NMR chemical shifts for nitrogenated aromatic compounds. ARKIVOC - Archive for Organic Chemistry, p. 113-122, 2020Tradução . . Disponível em: https://doi.org/10.24820/ark.5550190.p011.135. Acesso em: 05 dez. 2025.
APA
Oliveira, M. T. de, Alves, J. M. A., Morais, S. F. de A., & Braga, A. A. C. (2020). Prediction of 15N NMR chemical shifts for nitrogenated aromatic compounds. ARKIVOC - Archive for Organic Chemistry, 113-122. doi:10.24820/ark.5550190.p011.135
NLM
Oliveira MT de, Alves JMA, Morais SF de A, Braga AAC. Prediction of 15N NMR chemical shifts for nitrogenated aromatic compounds [Internet]. ARKIVOC - Archive for Organic Chemistry. 2020 ; 113-122.[citado 2025 dez. 05 ] Available from: https://doi.org/10.24820/ark.5550190.p011.135
Vancouver
Oliveira MT de, Alves JMA, Morais SF de A, Braga AAC. Prediction of 15N NMR chemical shifts for nitrogenated aromatic compounds [Internet]. ARKIVOC - Archive for Organic Chemistry. 2020 ; 113-122.[citado 2025 dez. 05 ] Available from: https://doi.org/10.24820/ark.5550190.p011.135
Artigo de periodico
Cascate reactions of progesterone by mycelia and culture broth from marine - derived fungus Aspergillus sydowii CBMAI 935 (2020)
Paula, Samuel Filipe Cardoso de ; Porto, Andre Luiz Meleiro
Fonte: Biocatalysis and Agricultural Biotechnology. Unidade: IQSC
Assuntos: QUÍMICA ORGÂNICA, ESTEROIDES, ÁGUA DO MAR
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ABNT
PAULA, Samuel Filipe Cardoso de e PORTO, Andre Luiz Meleiro. Cascate reactions of progesterone by mycelia and culture broth from marine - derived fungus Aspergillus sydowii CBMAI 935. Biocatalysis and Agricultural Biotechnology, v. 25, p. 101546, 2020Tradução . . Disponível em: https://doi.org/10.1016/j.bcab.2020.101546. Acesso em: 05 dez. 2025.
APA
Paula, S. F. C. de, & Porto, A. L. M. (2020). Cascate reactions of progesterone by mycelia and culture broth from marine - derived fungus Aspergillus sydowii CBMAI 935. Biocatalysis and Agricultural Biotechnology, 25, 101546. doi:10.1016/j.bcab.2020.101546
NLM
Paula SFC de, Porto ALM. Cascate reactions of progesterone by mycelia and culture broth from marine - derived fungus Aspergillus sydowii CBMAI 935 [Internet]. Biocatalysis and Agricultural Biotechnology. 2020 ; 25 101546.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.bcab.2020.101546
Vancouver
Paula SFC de, Porto ALM. Cascate reactions of progesterone by mycelia and culture broth from marine - derived fungus Aspergillus sydowii CBMAI 935 [Internet]. Biocatalysis and Agricultural Biotechnology. 2020 ; 25 101546.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.bcab.2020.101546
Artigo de periodico
One-pot synthesis of β-O-4 lignin models via the insertion of stable 2-diazo-1,3-dicarbonyls into O–H bonds (2020)
Dias, Rafael Mafra de Paula; Oliveira, Gabriela P. de; Burtoloso, Antonio Carlos Bender
Fonte: Organic & Biomolecular Chemistry. Unidade: IQSC
Assunto: QUÍMICA ORGÂNICA
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ABNT
DIAS, Rafael Mafra de Paula e OLIVEIRA, Gabriela P. de e BURTOLOSO, Antonio Carlos Bender. One-pot synthesis of β-O-4 lignin models via the insertion of stable 2-diazo-1,3-dicarbonyls into O–H bonds. Organic & Biomolecular Chemistry, v. 18, p. 4815–4823, 2020Tradução . . Disponível em: https://doi.org/10.1039/d0ob00800a. Acesso em: 05 dez. 2025.
APA
Dias, R. M. de P., Oliveira, G. P. de, & Burtoloso, A. C. B. (2020). One-pot synthesis of β-O-4 lignin models via the insertion of stable 2-diazo-1,3-dicarbonyls into O–H bonds. Organic & Biomolecular Chemistry, 18, 4815–4823. doi:10.1039/d0ob00800a
NLM
Dias RM de P, Oliveira GP de, Burtoloso ACB. One-pot synthesis of β-O-4 lignin models via the insertion of stable 2-diazo-1,3-dicarbonyls into O–H bonds [Internet]. Organic & Biomolecular Chemistry. 2020 ;18 4815–4823.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1039/d0ob00800a
Vancouver
Dias RM de P, Oliveira GP de, Burtoloso ACB. One-pot synthesis of β-O-4 lignin models via the insertion of stable 2-diazo-1,3-dicarbonyls into O–H bonds [Internet]. Organic & Biomolecular Chemistry. 2020 ;18 4815–4823.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1039/d0ob00800a
Artigo de periodico
HClO4-Al2O3 as a Prominent Catalyst in the Synthesis of 3,4- Dihydropyrimidin-2(1H)-ones/thiones under Environmentally Friendly Solvent Conditions (2020)
Zanin, Lucas Lima ; Porto, Andre Luiz Meleiro
Fonte: ChemistrySelect. Unidade: IQSC
Assuntos: QUÍMICA ORGÂNICA, CATALISADORES
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ABNT
ZANIN, Lucas Lima e PORTO, Andre Luiz Meleiro. HClO4-Al2O3 as a Prominent Catalyst in the Synthesis of 3,4- Dihydropyrimidin-2(1H)-ones/thiones under Environmentally Friendly Solvent Conditions. ChemistrySelect, v. 5, n. 28, p. 8604-8608, 2020Tradução . . Disponível em: https://doi.org/10.1002/slct.202001830. Acesso em: 05 dez. 2025.
APA
Zanin, L. L., & Porto, A. L. M. (2020). HClO4-Al2O3 as a Prominent Catalyst in the Synthesis of 3,4- Dihydropyrimidin-2(1H)-ones/thiones under Environmentally Friendly Solvent Conditions. ChemistrySelect, 5( 28), 8604-8608. doi:10.1002/slct.202001830
NLM
Zanin LL, Porto ALM. HClO4-Al2O3 as a Prominent Catalyst in the Synthesis of 3,4- Dihydropyrimidin-2(1H)-ones/thiones under Environmentally Friendly Solvent Conditions [Internet]. ChemistrySelect. 2020 ; 5( 28): 8604-8608.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1002/slct.202001830
Vancouver
Zanin LL, Porto ALM. HClO4-Al2O3 as a Prominent Catalyst in the Synthesis of 3,4- Dihydropyrimidin-2(1H)-ones/thiones under Environmentally Friendly Solvent Conditions [Internet]. ChemistrySelect. 2020 ; 5( 28): 8604-8608.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1002/slct.202001830
Artigo de periodico
An efficient approach for the synthesis of new (±)-coixspirolactams (2020)
Nascimento, Vinicius Rodrigues do; Suenaga, Melissa Lieko Souza; Andrade, Leandro Helgueira
Fonte: Organic & Biomolecular Chemistry. Unidade: IQ
Assuntos: ALCALOIDES, QUÍMICA ORGÂNICA
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ABNT
NASCIMENTO, Vinicius Rodrigues do e SUENAGA, Melissa Lieko Souza e ANDRADE, Leandro Helgueira. An efficient approach for the synthesis of new (±)-coixspirolactams. Organic & Biomolecular Chemistry, v. 18, p. 5458-5465, 2020Tradução . . Disponível em: https://doi.org/10.1039/d0ob01104e. Acesso em: 05 dez. 2025.
APA
Nascimento, V. R. do, Suenaga, M. L. S., & Andrade, L. H. (2020). An efficient approach for the synthesis of new (±)-coixspirolactams. Organic & Biomolecular Chemistry, 18, 5458-5465. doi:10.1039/d0ob01104e
NLM
Nascimento VR do, Suenaga MLS, Andrade LH. An efficient approach for the synthesis of new (±)-coixspirolactams [Internet]. Organic & Biomolecular Chemistry. 2020 ; 18 5458-5465.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1039/d0ob01104e
Vancouver
Nascimento VR do, Suenaga MLS, Andrade LH. An efficient approach for the synthesis of new (±)-coixspirolactams [Internet]. Organic & Biomolecular Chemistry. 2020 ; 18 5458-5465.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1039/d0ob01104e
Artigo de periodico
Enterovibrio baiacu sp. nov. (2020)
Azevedo, Gustavo Pitta Reis de; Mattsson, Hannah K ; Appolinario, Luciana R; Calegario, Gabriela; Leomil, Luciana; Walter, Juline M.; Campeão, Mariana; Tonon, Luciane Alessandra Chimetto ; Moreira, Ana Paula B; Vidal, Livia; Vieira, Verônica V.; Otsuki, Koko; Tschoeke, Diogo A; Swings, Jean; Thompson, Fabiano Lopes; Thompson, Cristiane Carneiro
Fonte: Current Microbiology. Unidade: IQSC
Assuntos: QUÍMICA ORGÂNICA, GENÔMICA, PEIXES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AZEVEDO, Gustavo Pitta Reis de et al. Enterovibrio baiacu sp. nov. Current Microbiology, v. 77, p. 154–157, 2020Tradução . . Disponível em: https://doi.org/10.1007/s00284-019-01785-7. Acesso em: 05 dez. 2025.
APA
Azevedo, G. P. R. de, Mattsson, H. K., Appolinario, L. R., Calegario, G., Leomil, L., Walter, J. M., et al. (2020). Enterovibrio baiacu sp. nov. Current Microbiology, 77, 154–157. doi:10.1007/s00284-019-01785-7
NLM
Azevedo GPR de, Mattsson HK, Appolinario LR, Calegario G, Leomil L, Walter JM, Campeão M, Tonon LAC, Moreira APB, Vidal L, Vieira VV, Otsuki K, Tschoeke DA, Swings J, Thompson FL, Thompson CC. Enterovibrio baiacu sp. nov. [Internet]. Current Microbiology. 2020 ; 77 154–157.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1007/s00284-019-01785-7
Vancouver
Azevedo GPR de, Mattsson HK, Appolinario LR, Calegario G, Leomil L, Walter JM, Campeão M, Tonon LAC, Moreira APB, Vidal L, Vieira VV, Otsuki K, Tschoeke DA, Swings J, Thompson FL, Thompson CC. Enterovibrio baiacu sp. nov. [Internet]. Current Microbiology. 2020 ; 77 154–157.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1007/s00284-019-01785-7
Artigo de periodico
Efficient and irreversible antibody–cysteine bioconjugation using carbonylacrylic reagents (2019)
Bernardim, Barbara; Matos, Maria J; Ferhati, Xhenti; Compañón, Ismael; Guerreiro, Ana; Akkapeddi, Padma; Burtoloso, Antonio Carlos Bender ; Jiménez-Osés, Gonzalo; Corzana, Francisco; Bernardes, Gonçalo J. L
Fonte: Nature Protocols. Unidade: IQSC
Assuntos: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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ABNT
BERNARDIM, Barbara et al. Efficient and irreversible antibody–cysteine bioconjugation using carbonylacrylic reagents. Nature Protocols, v. 14, n. Ja 2019, p. 86-99, 2019Tradução . . Disponível em: https://doi.org/10.1038/s41596-018-0083-9. Acesso em: 05 dez. 2025.
APA
Bernardim, B., Matos, M. J., Ferhati, X., Compañón, I., Guerreiro, A., Akkapeddi, P., et al. (2019). Efficient and irreversible antibody–cysteine bioconjugation using carbonylacrylic reagents. Nature Protocols, 14( Ja 2019), 86-99. doi:10.1038/s41596-018-0083-9
NLM
Bernardim B, Matos MJ, Ferhati X, Compañón I, Guerreiro A, Akkapeddi P, Burtoloso ACB, Jiménez-Osés G, Corzana F, Bernardes GJL. Efficient and irreversible antibody–cysteine bioconjugation using carbonylacrylic reagents [Internet]. Nature Protocols. 2019 ; 14( Ja 2019): 86-99.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1038/s41596-018-0083-9
Vancouver
Bernardim B, Matos MJ, Ferhati X, Compañón I, Guerreiro A, Akkapeddi P, Burtoloso ACB, Jiménez-Osés G, Corzana F, Bernardes GJL. Efficient and irreversible antibody–cysteine bioconjugation using carbonylacrylic reagents [Internet]. Nature Protocols. 2019 ; 14( Ja 2019): 86-99.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1038/s41596-018-0083-9
Artigo de periodico
Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity (2019)
Queiroz, Thayane M; Orozco, Erika Vanessa Meñaca ; Silva, Valdenizia; Santos, Luciano S.; Soares, Milena B.P.; Bezerra, Daniel P.; Porto, Andre Luiz Meleiro
Fonte: Heliyon. Unidade: IQSC
Assuntos: QUÍMICA ORGÂNICA, QUÍMICA FARMACÊUTICA, TOXICOLOGIA, CARCINOMA HEPATOCELULAR, ADENOCARCINOMA, MAMA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
QUEIROZ, Thayane M et al. Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity. Heliyon, v. 5, n. 9, 2019Tradução . . Disponível em: https://doi.org/10.1016/j.heliyon.2019.e02408. Acesso em: 05 dez. 2025.
APA
Queiroz, T. M., Orozco, E. V. M., Silva, V., Santos, L. S., Soares, M. B. P., Bezerra, D. P., & Porto, A. L. M. (2019). Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity. Heliyon, 5( 9). doi:10.1016/j.heliyon.2019.e02408
NLM
Queiroz TM, Orozco EVM, Silva V, Santos LS, Soares MBP, Bezerra DP, Porto ALM. Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity [Internet]. Heliyon. 2019 ; 5( 9):[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.heliyon.2019.e02408
Vancouver
Queiroz TM, Orozco EVM, Silva V, Santos LS, Soares MBP, Bezerra DP, Porto ALM. Semi-synthesis of β-keto-1,2,3-triazole derivatives from ethinylestradiol and evaluation of the cytotoxic activity [Internet]. Heliyon. 2019 ; 5( 9):[citado 2025 dez. 05 ] Available from: https://doi.org/10.1016/j.heliyon.2019.e02408
Artigo de periodico
Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides (2019)
Ahmad, Anees; Burtoloso, Antonio Carlos Bender
Fonte: Organic letters. Unidade: IQSC
Assunto: QUÍMICA ORGÂNICA
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ABNT
AHMAD, Anees e BURTOLOSO, Antonio Carlos Bender. Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides. Organic letters, v. 21, p. 6079-6083, 2019Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.9b02221. Acesso em: 05 dez. 2025.
APA
Ahmad, A., & Burtoloso, A. C. B. (2019). Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides. Organic letters, 21, 6079-6083. doi:10.1021/acs.orglett.9b02221
NLM
Ahmad A, Burtoloso ACB. Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides [Internet]. Organic letters. 2019 ;21 6079-6083.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/acs.orglett.9b02221
Vancouver
Ahmad A, Burtoloso ACB. Total Synthesis of (±)-Brussonol and (±)-Komaroviquinone via a Regioselective Cross-Electrophile Coupling of Aryl Bromides and Epoxides [Internet]. Organic letters. 2019 ;21 6079-6083.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1021/acs.orglett.9b02221
Artigo de periodico
Synthesis of 'alfa' chroacetophenones with NH4Cl/Oxone® in situ followed by bioreduction with whole cells of marine-derived fungi (2018)
Morais, Aline Teixeira do Brasil; Ferreira , Irlon Maciel; Jimenez, David Esteban Quintero; Porto, Andre Luiz Meleiro
Fonte: Biocatalysis and Agricultural Biotechnology. Unidade: IQSC
Assuntos: IRRADIAÇÃO, QUÍMICA ORGÂNICA
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ABNT
MORAIS, Aline Teixeira do Brasil et al. Synthesis of 'alfa' chroacetophenones with NH4Cl/Oxone® in situ followed by bioreduction with whole cells of marine-derived fungi. Biocatalysis and Agricultural Biotechnology, v. 16. p.314-319, 2018Tradução . . Disponível em: https://ac-els-cdn.ez67.periodicos.capes.gov.br/S1878818117304899/1-s2.0-S1878818117304899-main.pdf?_tid=0782d2f5-b272-4a6a-8ced-41606d54c061&acdnat=1537275142_0e6188642a295e58e17c682ba94934dd. Acesso em: 05 dez. 2025.
APA
Morais, A. T. do B., Ferreira , I. M., Jimenez, D. E. Q., & Porto, A. L. M. (2018). Synthesis of 'alfa' chroacetophenones with NH4Cl/Oxone® in situ followed by bioreduction with whole cells of marine-derived fungi. Biocatalysis and Agricultural Biotechnology, 16. p.314-319. doi:10.1016/j.bcab.2018.08.003
NLM
Morais AT do B, Ferreira IM, Jimenez DEQ, Porto ALM. Synthesis of 'alfa' chroacetophenones with NH4Cl/Oxone® in situ followed by bioreduction with whole cells of marine-derived fungi [Internet]. Biocatalysis and Agricultural Biotechnology. 2018 ;16. p.314-319[citado 2025 dez. 05 ] Available from: https://ac-els-cdn.ez67.periodicos.capes.gov.br/S1878818117304899/1-s2.0-S1878818117304899-main.pdf?_tid=0782d2f5-b272-4a6a-8ced-41606d54c061&acdnat=1537275142_0e6188642a295e58e17c682ba94934dd
Vancouver
Morais AT do B, Ferreira IM, Jimenez DEQ, Porto ALM. Synthesis of 'alfa' chroacetophenones with NH4Cl/Oxone® in situ followed by bioreduction with whole cells of marine-derived fungi [Internet]. Biocatalysis and Agricultural Biotechnology. 2018 ;16. p.314-319[citado 2025 dez. 05 ] Available from: https://ac-els-cdn.ez67.periodicos.capes.gov.br/S1878818117304899/1-s2.0-S1878818117304899-main.pdf?_tid=0782d2f5-b272-4a6a-8ced-41606d54c061&acdnat=1537275142_0e6188642a295e58e17c682ba94934dd
Artigo de periodico
How does the total charge and isomerism influence the Ru–NO ammine complexes? (2018)
Orenha, Renato Pereira ; Tfouni, Elia ; Galembeck, Sérgio Emanuel
Fonte: Physical Chemistry Chemical Physics. Unidade: FFCLRP
Assuntos: QUÍMICA ORGÂNICA, RUTÊNIO, ÓXIDO NÍTRICO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ORENHA, Renato Pereira e TFOUNI, Elia e GALEMBECK, Sérgio Emanuel. How does the total charge and isomerism influence the Ru–NO ammine complexes?. Physical Chemistry Chemical Physics, v. 20, n. 19, p. 13348-13356, 2018Tradução . . Disponível em: https://doi.org/10.1039/c8cp00865e. Acesso em: 05 dez. 2025.
APA
Orenha, R. P., Tfouni, E., & Galembeck, S. E. (2018). How does the total charge and isomerism influence the Ru–NO ammine complexes? Physical Chemistry Chemical Physics, 20( 19), 13348-13356. doi:10.1039/c8cp00865e
NLM
Orenha RP, Tfouni E, Galembeck SE. How does the total charge and isomerism influence the Ru–NO ammine complexes? [Internet]. Physical Chemistry Chemical Physics. 2018 ; 20( 19): 13348-13356.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1039/c8cp00865e
Vancouver
Orenha RP, Tfouni E, Galembeck SE. How does the total charge and isomerism influence the Ru–NO ammine complexes? [Internet]. Physical Chemistry Chemical Physics. 2018 ; 20( 19): 13348-13356.[citado 2025 dez. 05 ] Available from: https://doi.org/10.1039/c8cp00865e

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