ReP USP - Resultado da busca

Artigo de periodico
Synthesis, characterization and structural analysis of complexes from 2,2′:6′,2′′-terpyridine derivatives with transition metals (2024)
Perafan, Daniel Alexander Fajardo ; Arteaga, Danny ; Ellena, Javier ; Santiago, Pedro Henrique de Oliveira ; Arturo, Richard Fernando D'Vries ; Velasquez, Luis Alberto Lenis
Fonte: Acta Crystallographica C. Unidade: IFSC
Assuntos: CRISTALOGRAFIA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PERAFAN, Daniel Alexander Fajardo et al. Synthesis, characterization and structural analysis of complexes from 2,2′:6′,2′′-terpyridine derivatives with transition metals. Acta Crystallographica C, v. 80, n. 6, p. 200-211 + supporting information: s1-s27, 2024Tradução . . Disponível em: https://doi.org/10.1107/S2053229624004224. Acesso em: 28 ago. 2024.
APA
Perafan, D. A. F., Arteaga, D., Ellena, J., Santiago, P. H. de O., Arturo, R. F. D. 'V., & Velasquez, L. A. L. (2024). Synthesis, characterization and structural analysis of complexes from 2,2′:6′,2′′-terpyridine derivatives with transition metals. Acta Crystallographica C, 80( 6), 200-211 + supporting information: s1-s27. doi:10.1107/S2053229624004224
NLM
Perafan DAF, Arteaga D, Ellena J, Santiago PH de O, Arturo RFD'V, Velasquez LAL. Synthesis, characterization and structural analysis of complexes from 2,2′:6′,2′′-terpyridine derivatives with transition metals [Internet]. Acta Crystallographica C. 2024 ; 80( 6): 200-211 + supporting information: s1-s27.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1107/S2053229624004224
Vancouver
Perafan DAF, Arteaga D, Ellena J, Santiago PH de O, Arturo RFD'V, Velasquez LAL. Synthesis, characterization and structural analysis of complexes from 2,2′:6′,2′′-terpyridine derivatives with transition metals [Internet]. Acta Crystallographica C. 2024 ; 80( 6): 200-211 + supporting information: s1-s27.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1107/S2053229624004224
Artigo de periodico
Crystal structure of 1-(1,3-benzothiazol-2-yl)-3-(4-bromobenzoyl)thiourea (2024)
Sow, Salif; Thiam, Mariama; Odame, Felix; Thiam, Elhadj Ibrahima ; Diouf, Ousmane; Ellena, Javier ; Gaye, Mohamed ; Tshentu, Zenixole
Fonte: Acta Crystallographica E. Unidade: IFSC
Assuntos: CRISTALOGRAFIA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SOW, Salif et al. Crystal structure of 1-(1,3-benzothiazol-2-yl)-3-(4-bromobenzoyl)thiourea. Acta Crystallographica E, v. 80, p. 663-666 + supporting information, 2024Tradução . . Disponível em: https://doi.org/10.1107/S2056989024004742. Acesso em: 28 ago. 2024.
APA
Sow, S., Thiam, M., Odame, F., Thiam, E. I., Diouf, O., Ellena, J., et al. (2024). Crystal structure of 1-(1,3-benzothiazol-2-yl)-3-(4-bromobenzoyl)thiourea. Acta Crystallographica E, 80, 663-666 + supporting information. doi:10.1107/S2056989024004742
NLM
Sow S, Thiam M, Odame F, Thiam EI, Diouf O, Ellena J, Gaye M, Tshentu Z. Crystal structure of 1-(1,3-benzothiazol-2-yl)-3-(4-bromobenzoyl)thiourea [Internet]. Acta Crystallographica E. 2024 ; 80 663-666 + supporting information.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1107/S2056989024004742
Vancouver
Sow S, Thiam M, Odame F, Thiam EI, Diouf O, Ellena J, Gaye M, Tshentu Z. Crystal structure of 1-(1,3-benzothiazol-2-yl)-3-(4-bromobenzoyl)thiourea [Internet]. Acta Crystallographica E. 2024 ; 80 663-666 + supporting information.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1107/S2056989024004742
Artigo de periodico
X-ray diffraction and in vivo studies reveal the quinary structure of Trypanosoma cruzi nucleoside diphosphate kinase 1: a novel helical oligomer structure (2022)
Barroso, Juan Arturo Gomez ; Miranda, Mariana Reneé; Pereira, Claudio Alejandro; Garratt, Richard Charles ; Aguilar, Carlos Fernando
Fonte: Acta Crystallographica D. Unidade: IFSC
Assuntos: TRYPANOSOMA CRUZI, PLANEJAMENTO DE FÁRMACOS, CRISTALOGRAFIA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARROSO, Juan Arturo Gomez et al. X-ray diffraction and in vivo studies reveal the quinary structure of Trypanosoma cruzi nucleoside diphosphate kinase 1: a novel helical oligomer structure. Acta Crystallographica D, v. 78, n. Ja 2022, p. 30-42, 2022Tradução . . Disponível em: https://doi.org/10.1107/S2059798321011219. Acesso em: 28 ago. 2024.
APA
Barroso, J. A. G., Miranda, M. R., Pereira, C. A., Garratt, R. C., & Aguilar, C. F. (2022). X-ray diffraction and in vivo studies reveal the quinary structure of Trypanosoma cruzi nucleoside diphosphate kinase 1: a novel helical oligomer structure. Acta Crystallographica D, 78( Ja 2022), 30-42. doi:10.1107/S2059798321011219
NLM
Barroso JAG, Miranda MR, Pereira CA, Garratt RC, Aguilar CF. X-ray diffraction and in vivo studies reveal the quinary structure of Trypanosoma cruzi nucleoside diphosphate kinase 1: a novel helical oligomer structure [Internet]. Acta Crystallographica D. 2022 ; 78( Ja 2022): 30-42.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1107/S2059798321011219
Vancouver
Barroso JAG, Miranda MR, Pereira CA, Garratt RC, Aguilar CF. X-ray diffraction and in vivo studies reveal the quinary structure of Trypanosoma cruzi nucleoside diphosphate kinase 1: a novel helical oligomer structure [Internet]. Acta Crystallographica D. 2022 ; 78( Ja 2022): 30-42.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1107/S2059798321011219
Trabalho de evento-resumo periodico
Co-crystal structure of a dinuclear (Zn-Y) and a trinuclear (Zn-Y-Zn) complexes derived from a Schiff base ligand (2021)
Thiam, Ibrahima Elhadji; Gaye, Mohamed Lamine; Ellena, Javier ; Sarr, Mamour; Diop, Mayoro; Álvarez, Natalia; Barry, Aliou Hamady
Fonte: Acta Crystallographica A. Nome do evento: General Assembly and Congress of the International Union of Crystallography - IUCr. Unidade: IFSC
Assuntos: CRISTALOGRAFIA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
THIAM, Ibrahima Elhadji et al. Co-crystal structure of a dinuclear (Zn-Y) and a trinuclear (Zn-Y-Zn) complexes derived from a Schiff base ligand. Acta Crystallographica A. Chester: International Union of Crystallography - IUCr. Disponível em: https://doi.org/10.1107/S010876732108555X. Acesso em: 28 ago. 2024. , 2021
APA
Thiam, I. E., Gaye, M. L., Ellena, J., Sarr, M., Diop, M., Álvarez, N., & Barry, A. H. (2021). Co-crystal structure of a dinuclear (Zn-Y) and a trinuclear (Zn-Y-Zn) complexes derived from a Schiff base ligand. Acta Crystallographica A. Chester: International Union of Crystallography - IUCr. doi:10.1107/S010876732108555X
NLM
Thiam IE, Gaye ML, Ellena J, Sarr M, Diop M, Álvarez N, Barry AH. Co-crystal structure of a dinuclear (Zn-Y) and a trinuclear (Zn-Y-Zn) complexes derived from a Schiff base ligand [Internet]. Acta Crystallographica A. 2021 ; A77 C1152.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1107/S010876732108555X
Vancouver
Thiam IE, Gaye ML, Ellena J, Sarr M, Diop M, Álvarez N, Barry AH. Co-crystal structure of a dinuclear (Zn-Y) and a trinuclear (Zn-Y-Zn) complexes derived from a Schiff base ligand [Internet]. Acta Crystallographica A. 2021 ; A77 C1152.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1107/S010876732108555X
Artigo de periodico
Synthesis, spectroscopic (FT-IR and UV-Vis), crystallographic and theoretical studies, and a molecular docking simulation of an imatinib-like template (2019)
Moreno-Fuquen, Rodolfo; Arango-Daraviña, Kevin; Garcia, Esteban; Clavijo, Juan Carlos Tenorio; Ellena, Javier
Fonte: Acta Crystallographica C. Unidade: IFSC
Assuntos: CRISTALOGRAFIA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MORENO-FUQUEN, Rodolfo et al. Synthesis, spectroscopic (FT-IR and UV-Vis), crystallographic and theoretical studies, and a molecular docking simulation of an imatinib-like template. Acta Crystallographica C, v. 75, p. 1681-1689, 2019Tradução . . Disponível em: https://doi.org/10.1107/S2053229619015523. Acesso em: 28 ago. 2024.
APA
Moreno-Fuquen, R., Arango-Daraviña, K., Garcia, E., Clavijo, J. C. T., & Ellena, J. (2019). Synthesis, spectroscopic (FT-IR and UV-Vis), crystallographic and theoretical studies, and a molecular docking simulation of an imatinib-like template. Acta Crystallographica C, 75, 1681-1689. doi:10.1107/S2053229619015523
NLM
Moreno-Fuquen R, Arango-Daraviña K, Garcia E, Clavijo JCT, Ellena J. Synthesis, spectroscopic (FT-IR and UV-Vis), crystallographic and theoretical studies, and a molecular docking simulation of an imatinib-like template [Internet]. Acta Crystallographica C. 2019 ; 75 1681-1689.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1107/S2053229619015523
Vancouver
Moreno-Fuquen R, Arango-Daraviña K, Garcia E, Clavijo JCT, Ellena J. Synthesis, spectroscopic (FT-IR and UV-Vis), crystallographic and theoretical studies, and a molecular docking simulation of an imatinib-like template [Internet]. Acta Crystallographica C. 2019 ; 75 1681-1689.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1107/S2053229619015523
Artigo de periodico
Crystal structures of two CuII compounds: catenapoly[[ chloridocopper(II)]-l-N-[ethoxy(pyridin-2- yl)methylidene]-N0-[oxido(pyridin-3-yl)methylidene] hydrazine-j4N,N0,O:N00] and di-l-chlorido- 1:4j2Cl:Cl-2:3j2Cl:Cl-dichlorido-2jCl,4jCl-bis- [l3-ethoxy(pyridin-2-yl)methanolato-1:2:3j3O:- N,O:O;1:3:4j3O:O:N,O]bis[l2-ethoxy(pyridin-2- yl)methanolato-1:2j3N,O:O;3:4j3N,O:O]tetracopper( II) (2019)
Sall, Ousmane; Tamboura, Farba Bouyagui; Sy, Adama; Barry, Aliou Hamady; Thiam, Elhadj Ibrahima; Mohamed, Gaye; Ellena, Javier
Fonte: Acta Crystallographica E. Unidade: IFSC
Assuntos: CRISTALOGRAFIA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SALL, Ousmane et al. Crystal structures of two CuII compounds: catenapoly[[ chloridocopper(II)]-l-N-[ethoxy(pyridin-2- yl)methylidene]-N0-[oxido(pyridin-3-yl)methylidene] hydrazine-j4N,N0,O:N00] and di-l-chlorido- 1:4j2Cl:Cl-2:3j2Cl:Cl-dichlorido-2jCl,4jCl-bis- [l3-ethoxy(pyridin-2-yl)methanolato-1:2:3j3O:- N,O:O;1:3:4j3O:O:N,O]bis[l2-ethoxy(pyridin-2- yl)methanolato-1:2j3N,O:O;3:4j3N,O:O]tetracopper( II). Acta Crystallographica E, v. 75, p. 1069-1075, 2019Tradução . . Disponível em: https://doi.org/10.1107/S2056989019008922. Acesso em: 28 ago. 2024.
APA
Sall, O., Tamboura, F. B., Sy, A., Barry, A. H., Thiam, E. I., Mohamed, G., & Ellena, J. (2019). Crystal structures of two CuII compounds: catenapoly[[ chloridocopper(II)]-l-N-[ethoxy(pyridin-2- yl)methylidene]-N0-[oxido(pyridin-3-yl)methylidene] hydrazine-j4N,N0,O:N00] and di-l-chlorido- 1:4j2Cl:Cl-2:3j2Cl:Cl-dichlorido-2jCl,4jCl-bis- [l3-ethoxy(pyridin-2-yl)methanolato-1:2:3j3O:- N,O:O;1:3:4j3O:O:N,O]bis[l2-ethoxy(pyridin-2- yl)methanolato-1:2j3N,O:O;3:4j3N,O:O]tetracopper( II). Acta Crystallographica E, 75, 1069-1075. doi:10.1107/S2056989019008922
NLM
Sall O, Tamboura FB, Sy A, Barry AH, Thiam EI, Mohamed G, Ellena J. Crystal structures of two CuII compounds: catenapoly[[ chloridocopper(II)]-l-N-[ethoxy(pyridin-2- yl)methylidene]-N0-[oxido(pyridin-3-yl)methylidene] hydrazine-j4N,N0,O:N00] and di-l-chlorido- 1:4j2Cl:Cl-2:3j2Cl:Cl-dichlorido-2jCl,4jCl-bis- [l3-ethoxy(pyridin-2-yl)methanolato-1:2:3j3O:- N,O:O;1:3:4j3O:O:N,O]bis[l2-ethoxy(pyridin-2- yl)methanolato-1:2j3N,O:O;3:4j3N,O:O]tetracopper( II) [Internet]. Acta Crystallographica E. 2019 ; 75 1069-1075.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1107/S2056989019008922
Vancouver
Sall O, Tamboura FB, Sy A, Barry AH, Thiam EI, Mohamed G, Ellena J. Crystal structures of two CuII compounds: catenapoly[[ chloridocopper(II)]-l-N-[ethoxy(pyridin-2- yl)methylidene]-N0-[oxido(pyridin-3-yl)methylidene] hydrazine-j4N,N0,O:N00] and di-l-chlorido- 1:4j2Cl:Cl-2:3j2Cl:Cl-dichlorido-2jCl,4jCl-bis- [l3-ethoxy(pyridin-2-yl)methanolato-1:2:3j3O:- N,O:O;1:3:4j3O:O:N,O]bis[l2-ethoxy(pyridin-2- yl)methanolato-1:2j3N,O:O;3:4j3N,O:O]tetracopper( II) [Internet]. Acta Crystallographica E. 2019 ; 75 1069-1075.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1107/S2056989019008922
Artigo de periodico
The preparation of benzyl esters using stoichiometric niobium (V) chloride versus niobium grafted SiO2 catalyst: A comparison study (2018)
Barbosa, Sandro L.; Lima, Camila D.; Almeida, Melina A. R.; Mourão, Larissa S.; Ottone, Myrlene; Nelson, David L.; Klein, Stanlei I.; Zanatta, Lucas D. ; Clososki, Giuliano Cesar ; Caires, Franco J. ; Nassar, Eduardo J.; Hurtado, Gabriela R.
Fonte: Heliyon. Unidades: FCFRP, FFCLRP
Assuntos: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, NIÓBIO, CARBONATOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BARBOSA, Sandro L. et al. The preparation of benzyl esters using stoichiometric niobium (V) chloride versus niobium grafted SiO2 catalyst: A comparison study. Heliyon, v. 4, n. 3, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.heliyon.2018.e00571. Acesso em: 28 ago. 2024.
APA
Barbosa, S. L., Lima, C. D., Almeida, M. A. R., Mourão, L. S., Ottone, M., Nelson, D. L., et al. (2018). The preparation of benzyl esters using stoichiometric niobium (V) chloride versus niobium grafted SiO2 catalyst: A comparison study. Heliyon, 4( 3). doi:10.1016/j.heliyon.2018.e00571
NLM
Barbosa SL, Lima CD, Almeida MAR, Mourão LS, Ottone M, Nelson DL, Klein SI, Zanatta LD, Clososki GC, Caires FJ, Nassar EJ, Hurtado GR. The preparation of benzyl esters using stoichiometric niobium (V) chloride versus niobium grafted SiO2 catalyst: A comparison study [Internet]. Heliyon. 2018 ; 4( 3):[citado 2024 ago. 28 ] Available from: https://doi.org/10.1016/j.heliyon.2018.e00571
Vancouver
Barbosa SL, Lima CD, Almeida MAR, Mourão LS, Ottone M, Nelson DL, Klein SI, Zanatta LD, Clososki GC, Caires FJ, Nassar EJ, Hurtado GR. The preparation of benzyl esters using stoichiometric niobium (V) chloride versus niobium grafted SiO2 catalyst: A comparison study [Internet]. Heliyon. 2018 ; 4( 3):[citado 2024 ago. 28 ] Available from: https://doi.org/10.1016/j.heliyon.2018.e00571
Artigo de periodico
Modulating the DNA cleavage ability of copper(II) Schiff bases through ternary complex formation (2018)
Viqueira, Joaquín; Durán, María L.; García-Vázquez, José A.; Castro, Jesús; Platas-Iglesias, Carlos; Esteban-Gómez, David; Alzuet-Piña, Gloria; Moldes, Angeles; Nascimento, Otaciro Rangel
Fonte: New Journal of Chemistry. Unidade: IFSC
Assuntos: QUÍMICA ORGÂNICA, DNA, NANOPARTÍCULAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VIQUEIRA, Joaquín et al. Modulating the DNA cleavage ability of copper(II) Schiff bases through ternary complex formation. New Journal of Chemistry, v. 42, n. 18, p. 15170-15183, 2018Tradução . . Disponível em: https://doi.org/10.1039/c8nj03292k. Acesso em: 28 ago. 2024.
APA
Viqueira, J., Durán, M. L., García-Vázquez, J. A., Castro, J., Platas-Iglesias, C., Esteban-Gómez, D., et al. (2018). Modulating the DNA cleavage ability of copper(II) Schiff bases through ternary complex formation. New Journal of Chemistry, 42( 18), 15170-15183. doi:10.1039/c8nj03292k
NLM
Viqueira J, Durán ML, García-Vázquez JA, Castro J, Platas-Iglesias C, Esteban-Gómez D, Alzuet-Piña G, Moldes A, Nascimento OR. Modulating the DNA cleavage ability of copper(II) Schiff bases through ternary complex formation [Internet]. New Journal of Chemistry. 2018 ; 42( 18): 15170-15183.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1039/c8nj03292k
Vancouver
Viqueira J, Durán ML, García-Vázquez JA, Castro J, Platas-Iglesias C, Esteban-Gómez D, Alzuet-Piña G, Moldes A, Nascimento OR. Modulating the DNA cleavage ability of copper(II) Schiff bases through ternary complex formation [Internet]. New Journal of Chemistry. 2018 ; 42( 18): 15170-15183.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1039/c8nj03292k
Artigo de periodico
{1-[1-(2-Hydroxyphenyl)ethylidene]-2-(pyridin-2-yl-kN)hydrazine-k2N′,O}{1-[1-(2-oxidophenyl)ethylidene]-2-(pyridin-2-yl-kN)hydrazine-k2N′,O}nickelate(II) nitrate hemihydrate (2018)
Mamour, Sarr; Mayoro, Diop; Ibrahima, Thiam Elhadj; Mohamed, Gaye; Hamady, Barry Aliou; Ellena, Javier
Fonte: Acta Crystallographica E. Unidade: IFSC
Assuntos: CRISTALOGRAFIA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MAMOUR, Sarr et al. {1-[1-(2-Hydroxyphenyl)ethylidene]-2-(pyridin-2-yl-kN)hydrazine-k2N′,O}{1-[1-(2-oxidophenyl)ethylidene]-2-(pyridin-2-yl-kN)hydrazine-k2N′,O}nickelate(II) nitrate hemihydrate. Acta Crystallographica E, v. 74, p. 642-645, 2018Tradução . . Disponível em: https://doi.org/10.1107/S2056989018005261. Acesso em: 28 ago. 2024.
APA
Mamour, S., Mayoro, D., Ibrahima, T. E., Mohamed, G., Hamady, B. A., & Ellena, J. (2018). {1-[1-(2-Hydroxyphenyl)ethylidene]-2-(pyridin-2-yl-kN)hydrazine-k2N′,O}{1-[1-(2-oxidophenyl)ethylidene]-2-(pyridin-2-yl-kN)hydrazine-k2N′,O}nickelate(II) nitrate hemihydrate. Acta Crystallographica E, 74, 642-645. doi:10.1107/S2056989018005261
NLM
Mamour S, Mayoro D, Ibrahima TE, Mohamed G, Hamady BA, Ellena J. {1-[1-(2-Hydroxyphenyl)ethylidene]-2-(pyridin-2-yl-kN)hydrazine-k2N′,O}{1-[1-(2-oxidophenyl)ethylidene]-2-(pyridin-2-yl-kN)hydrazine-k2N′,O}nickelate(II) nitrate hemihydrate [Internet]. Acta Crystallographica E. 2018 ; 74 642-645.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1107/S2056989018005261
Vancouver
Mamour S, Mayoro D, Ibrahima TE, Mohamed G, Hamady BA, Ellena J. {1-[1-(2-Hydroxyphenyl)ethylidene]-2-(pyridin-2-yl-kN)hydrazine-k2N′,O}{1-[1-(2-oxidophenyl)ethylidene]-2-(pyridin-2-yl-kN)hydrazine-k2N′,O}nickelate(II) nitrate hemihydrate [Internet]. Acta Crystallographica E. 2018 ; 74 642-645.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1107/S2056989018005261
Artigo de periodico
Intramolecular radical cyclization approach to access highly substituted indolines and 2,3-dihydrobenzofurans under visible-light (2018)
Caiuby, Clarice A. D.; Ali, Akbar; Santana, Vinicius T.; Lucas, Francisco W. S.; Santos, Marilia S.; Corrêa, Arlene G.; Nascimento, Otaciro Rangel; Jiang, Hao; Paixão, Márcio W.
Fonte: RSC Advances. Unidade: IFSC
Assuntos: QUÍMICA ORGÂNICA, COMPOSTOS HETEROCÍCLICOS, RESSONÂNCIA PARAMAGNÉTICA ELETRÔNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CAIUBY, Clarice A. D. et al. Intramolecular radical cyclization approach to access highly substituted indolines and 2,3-dihydrobenzofurans under visible-light. RSC Advances, v. 8, n. 23, p. 12879-12886, 2018Tradução . . Disponível em: https://doi.org/10.1039/c8ra01787e. Acesso em: 28 ago. 2024.
APA
Caiuby, C. A. D., Ali, A., Santana, V. T., Lucas, F. W. S., Santos, M. S., Corrêa, A. G., et al. (2018). Intramolecular radical cyclization approach to access highly substituted indolines and 2,3-dihydrobenzofurans under visible-light. RSC Advances, 8( 23), 12879-12886. doi:10.1039/c8ra01787e
NLM
Caiuby CAD, Ali A, Santana VT, Lucas FWS, Santos MS, Corrêa AG, Nascimento OR, Jiang H, Paixão MW. Intramolecular radical cyclization approach to access highly substituted indolines and 2,3-dihydrobenzofurans under visible-light [Internet]. RSC Advances. 2018 ; 8( 23): 12879-12886.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1039/c8ra01787e
Vancouver
Caiuby CAD, Ali A, Santana VT, Lucas FWS, Santos MS, Corrêa AG, Nascimento OR, Jiang H, Paixão MW. Intramolecular radical cyclization approach to access highly substituted indolines and 2,3-dihydrobenzofurans under visible-light [Internet]. RSC Advances. 2018 ; 8( 23): 12879-12886.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1039/c8ra01787e
Artigo de periodico
Exploiting supramolecular interactions to produce bevacizumab-loaded nanoparticles for potential mucosal delivery (2018)
Ferreira, Leonardo M. B.; Alonso, Jovan D; Kiill, Charlene P; Ferreira, Natália N; Buzzá, Hilde Harb ; Godoi, Denis R. Martins de; Britto, Douglas de; Assis, Odílio Benedito Garrido de ; Seraphim, Thiago Vargas ; Borges, Julio Cesar ; Gremião, Maria Palmira Daflon
Fonte: European Polymer Journal. Unidade: IQSC
Assuntos: QUÍMICA ORGÂNICA, NANOPARTÍCULAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
FERREIRA, Leonardo M. B. et al. Exploiting supramolecular interactions to produce bevacizumab-loaded nanoparticles for potential mucosal delivery. European Polymer Journal, v. 103, p. 238-250, 2018Tradução . . Disponível em: https://doi.org/10.1016/j.eurpolymj.2018.04.013. Acesso em: 28 ago. 2024.
APA
Ferreira, L. M. B., Alonso, J. D., Kiill, C. P., Ferreira, N. N., Buzzá, H. H., Godoi, D. R. M. de, et al. (2018). Exploiting supramolecular interactions to produce bevacizumab-loaded nanoparticles for potential mucosal delivery. European Polymer Journal, 103, 238-250. doi:10.1016/j.eurpolymj.2018.04.013
NLM
Ferreira LMB, Alonso JD, Kiill CP, Ferreira NN, Buzzá HH, Godoi DRM de, Britto D de, Assis OBG de, Seraphim TV, Borges JC, Gremião MPD. Exploiting supramolecular interactions to produce bevacizumab-loaded nanoparticles for potential mucosal delivery [Internet]. European Polymer Journal. 2018 ; 103 238-250.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1016/j.eurpolymj.2018.04.013
Vancouver
Ferreira LMB, Alonso JD, Kiill CP, Ferreira NN, Buzzá HH, Godoi DRM de, Britto D de, Assis OBG de, Seraphim TV, Borges JC, Gremião MPD. Exploiting supramolecular interactions to produce bevacizumab-loaded nanoparticles for potential mucosal delivery [Internet]. European Polymer Journal. 2018 ; 103 238-250.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1016/j.eurpolymj.2018.04.013
Trabalho de evento-resumo
Electrophilic alkynylation using hypervalent iodine reagents (2017)
Teodoro, Bruno Vinicius Motta; Silva Junior, Luiz Fernando da
Fonte: Proceedings. Nome do evento: World Chemistry Congress. Unidade: IQ
Assuntos: REAGENTES ORGÂNICOS, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
TEODORO, Bruno Vinicius Motta e SILVA JUNIOR, Luiz Fernando da. Electrophilic alkynylation using hypervalent iodine reagents. 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 28 ago. 2024.
APA
Teodoro, B. V. M., & Silva Junior, L. F. da. (2017). Electrophilic alkynylation using hypervalent iodine reagents. In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Teodoro BVM, Silva Junior LF da. Electrophilic alkynylation using hypervalent iodine reagents [Internet]. Proceedings. 2017 ;[citado 2024 ago. 28 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Teodoro BVM, Silva Junior LF da. Electrophilic alkynylation using hypervalent iodine reagents [Internet]. Proceedings. 2017 ;[citado 2024 ago. 28 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Trabalho de evento-resumo
Cyclofunctionalizations using iodine/iodine(III) (2017)
Scarassati Filho, Paulo; Silva Junior, Luiz Fernando da
Fonte: Proceedings. Nome do evento: World Chemistry Congress. Unidade: IQ
Assuntos: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SCARASSATI FILHO, Paulo e SILVA JUNIOR, Luiz Fernando da. Cyclofunctionalizations using iodine/iodine(III). 2017, Anais.. Durham: International Union of Pure and Applied Chemistry (IUPAC), 2017. Disponível em: http://www.neopixdmi.com.br/@mci/iupac2017/. Acesso em: 28 ago. 2024.
APA
Scarassati Filho, P., & Silva Junior, L. F. da. (2017). Cyclofunctionalizations using iodine/iodine(III). In Proceedings. Durham: International Union of Pure and Applied Chemistry (IUPAC). Recuperado de http://www.neopixdmi.com.br/@mci/iupac2017/
NLM
Scarassati Filho P, Silva Junior LF da. Cyclofunctionalizations using iodine/iodine(III) [Internet]. Proceedings. 2017 ;[citado 2024 ago. 28 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Vancouver
Scarassati Filho P, Silva Junior LF da. Cyclofunctionalizations using iodine/iodine(III) [Internet]. Proceedings. 2017 ;[citado 2024 ago. 28 ] Available from: http://www.neopixdmi.com.br/@mci/iupac2017/
Artigo de periodico
Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl (2017)
Bozzini, Leandro A; Batista, João H. C.; Mello, Murilo B. M. de; Vessecchi, Ricardo; Clososki, Giuliano Cesar
Fonte: Tetrahedron Letters. Unidades: FFCLRP, FCFRP
Assuntos: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA, PRODUTOS NATURAIS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BOZZINI, Leandro A et al. Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl. Tetrahedron Letters, v. 58, p. 4186-4190, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2017.09.051. Acesso em: 28 ago. 2024.
APA
Bozzini, L. A., Batista, J. H. C., Mello, M. B. M. de, Vessecchi, R., & Clososki, G. C. (2017). Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl. Tetrahedron Letters, 58, 4186-4190. doi:10.1016/j.tetlet.2017.09.051
NLM
Bozzini LA, Batista JHC, Mello MBM de, Vessecchi R, Clososki GC. Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl [Internet]. Tetrahedron Letters. 2017 ; 58 4186-4190.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2017.09.051
Vancouver
Bozzini LA, Batista JHC, Mello MBM de, Vessecchi R, Clososki GC. Selective functionalization of cyano-phenyl-2-oxazolines using TMPMgCl.LiCl [Internet]. Tetrahedron Letters. 2017 ; 58 4186-4190.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2017.09.051
Artigo de periodico
Extractive biocatalysis in the asymmetric reduction of α-alkyl, β-aryl enones by Baker's yeast (2017)
Silva, Rafaela M.; Okano, Laura Tiemi; Rodrigues, J. Augusto R.; Clososki, Giuliano Cesar
Fonte: Tetrahedron : Asymmetry. Unidades: FCFRP, FFCLRP
Assuntos: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA, Rafaela M. et al. Extractive biocatalysis in the asymmetric reduction of α-alkyl, β-aryl enones by Baker's yeast. Tetrahedron : Asymmetry, v. 28, p. 939-944, 2017Tradução . . Disponível em: https://doi.org/10.1016/j.tetasy.2017.05.009. Acesso em: 28 ago. 2024.
APA
Silva, R. M., Okano, L. T., Rodrigues, J. A. R., & Clososki, G. C. (2017). Extractive biocatalysis in the asymmetric reduction of α-alkyl, β-aryl enones by Baker's yeast. Tetrahedron : Asymmetry, 28, 939-944. doi:10.1016/j.tetasy.2017.05.009
NLM
Silva RM, Okano LT, Rodrigues JAR, Clososki GC. Extractive biocatalysis in the asymmetric reduction of α-alkyl, β-aryl enones by Baker's yeast [Internet]. Tetrahedron : Asymmetry. 2017 ; 28 939-944.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1016/j.tetasy.2017.05.009
Vancouver
Silva RM, Okano LT, Rodrigues JAR, Clososki GC. Extractive biocatalysis in the asymmetric reduction of α-alkyl, β-aryl enones by Baker's yeast [Internet]. Tetrahedron : Asymmetry. 2017 ; 28 939-944.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1016/j.tetasy.2017.05.009
Artigo de periodico
Fast synthesis of amides from ethyl salicylate under microwave radiation in a solvent-free system (2017)
Lima, Rafaely Nascimento; Silva, Valdenizia R.; Santos, Luciano de S.; Bezerra, Daniel P; Soares, Milena Botelho Pereira; Porto, Andre Luiz Meleiro
Fonte: RSC Advances. Unidade: IQSC
Assuntos: QUÍMICA ORGÂNICA, ESPECTROMETRIA DE MASSAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
LIMA, Rafaely Nascimento et al. Fast synthesis of amides from ethyl salicylate under microwave radiation in a solvent-free system. RSC Advances, v. 7, n. 89, p. 56566-56574, 2017Tradução . . Disponível em: https://doi.org/10.1039/c7ra11434f. Acesso em: 28 ago. 2024.
APA
Lima, R. N., Silva, V. R., Santos, L. de S., Bezerra, D. P., Soares, M. B. P., & Porto, A. L. M. (2017). Fast synthesis of amides from ethyl salicylate under microwave radiation in a solvent-free system. RSC Advances, 7( 89), 56566-56574. doi:10.1039/c7ra11434f
NLM
Lima RN, Silva VR, Santos L de S, Bezerra DP, Soares MBP, Porto ALM. Fast synthesis of amides from ethyl salicylate under microwave radiation in a solvent-free system [Internet]. RSC Advances. 2017 ; 7( 89): 56566-56574.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1039/c7ra11434f
Vancouver
Lima RN, Silva VR, Santos L de S, Bezerra DP, Soares MBP, Porto ALM. Fast synthesis of amides from ethyl salicylate under microwave radiation in a solvent-free system [Internet]. RSC Advances. 2017 ; 7( 89): 56566-56574.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1039/c7ra11434f
Artigo de periodico
Strain-induced spin crossover and spin-polarized currents in a prototype graphene nanoribbon (2016)
Caro, Rodrigo Castellanos; Santos, Maria Cristina dos
Fonte: PHYSICAL CHEMISTRY CHEMICAL PHYSICS. Unidade: IF
Assuntos: SPIN, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
CARO, Rodrigo Castellanos e SANTOS, Maria Cristina dos. Strain-induced spin crossover and spin-polarized currents in a prototype graphene nanoribbon. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, v. 18, n. ju 2016, p. 16451-16456, 2016Tradução . . Disponível em: http://pubs.rsc.org/en/Content/ArticleLanding/2016/CP/c6cp02000c#!divAbstract. Acesso em: 28 ago. 2024.
APA
Caro, R. C., & Santos, M. C. dos. (2016). Strain-induced spin crossover and spin-polarized currents in a prototype graphene nanoribbon. PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 18( ju 2016), 16451-16456. doi:10.1039/c6cp02000c
NLM
Caro RC, Santos MC dos. Strain-induced spin crossover and spin-polarized currents in a prototype graphene nanoribbon [Internet]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS. 2016 ; 18( ju 2016): 16451-16456.[citado 2024 ago. 28 ] Available from: http://pubs.rsc.org/en/Content/ArticleLanding/2016/CP/c6cp02000c#!divAbstract
Vancouver
Caro RC, Santos MC dos. Strain-induced spin crossover and spin-polarized currents in a prototype graphene nanoribbon [Internet]. PHYSICAL CHEMISTRY CHEMICAL PHYSICS. 2016 ; 18( ju 2016): 16451-16456.[citado 2024 ago. 28 ] Available from: http://pubs.rsc.org/en/Content/ArticleLanding/2016/CP/c6cp02000c#!divAbstract
Artigo de periodico
Sodium lignosulfonate as a renewable stabilizing agent for aqueous alumina suspensions (2016)
Megiatto Junior, Jackson Dirceu; Cerrutti, Bianca Machado; Frollini, Elisabete
Fonte: International Journal of Biological Macromolecules. Unidade: IQSC
Assunto: QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
MEGIATTO JUNIOR, Jackson Dirceu e CERRUTTI, Bianca Machado e FROLLINI, Elisabete. Sodium lignosulfonate as a renewable stabilizing agent for aqueous alumina suspensions. International Journal of Biological Macromolecules, v. 82, p. 927-932, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.ijbiomac.2015.11.004. Acesso em: 28 ago. 2024.
APA
Megiatto Junior, J. D., Cerrutti, B. M., & Frollini, E. (2016). Sodium lignosulfonate as a renewable stabilizing agent for aqueous alumina suspensions. International Journal of Biological Macromolecules, 82, 927-932. doi:10.1016/j.ijbiomac.2015.11.004
NLM
Megiatto Junior JD, Cerrutti BM, Frollini E. Sodium lignosulfonate as a renewable stabilizing agent for aqueous alumina suspensions [Internet]. International Journal of Biological Macromolecules. 2016 ; 82 927-932.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1016/j.ijbiomac.2015.11.004
Vancouver
Megiatto Junior JD, Cerrutti BM, Frollini E. Sodium lignosulfonate as a renewable stabilizing agent for aqueous alumina suspensions [Internet]. International Journal of Biological Macromolecules. 2016 ; 82 927-932.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1016/j.ijbiomac.2015.11.004
Artigo de periodico
On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds (2016)
Avila, Thais C; Reginato, Marcelo M; Di Vitta, Cláudio ; Ducati, Lucas Colucci ; Andrade, Leandro Helgueira ; Marzorati, Liliana
Fonte: Tetrahedrom Letters. Unidade: IQ
Assuntos: QUÍMICA ORGÂNICA, COMPOSTOS ORGÂNICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
AVILA, Thais C et al. On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds. Tetrahedrom Letters, v. 57, p. 2152-2157, 2016Tradução . . Disponível em: https://doi.org/10.1016/j.tetlet.2016.03.109. Acesso em: 28 ago. 2024.
APA
Avila, T. C., Reginato, M. M., Di Vitta, C., Ducati, L. C., Andrade, L. H., & Marzorati, L. (2016). On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds. Tetrahedrom Letters, 57, 2152-2157. doi:10.1016/j.tetlet.2016.03.109
NLM
Avila TC, Reginato MM, Di Vitta C, Ducati LC, Andrade LH, Marzorati L. On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds [Internet]. Tetrahedrom Letters. 2016 ; 57 2152-2157.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2016.03.109
Vancouver
Avila TC, Reginato MM, Di Vitta C, Ducati LC, Andrade LH, Marzorati L. On the intermolecular interaction of N-benzylquininium chloride or quinine with some carbonyl group containing compounds [Internet]. Tetrahedrom Letters. 2016 ; 57 2152-2157.[citado 2024 ago. 28 ] Available from: https://doi.org/10.1016/j.tetlet.2016.03.109
Artigo de periodico
Stoichiometric and irreversible cysteine-selective protein modification using carbonylacrylic reagents (2016)
Bernardim, Barbara; Cal, Pedro M. S. D.; Matos, Maria J.; Oliveira, Bruno L.; Martínez-Sáez, Nuria; Albuquerque, Inês S; Perkins, Elizabeth; Corzana, Francisco; Burtoloso, Antonio Carlos Bender ; Jiménez-Osés, Gonzalo; Bernardes, Gonçalo L. L.
Fonte: Nature Communications. Unidade: IQSC
Assuntos: QUÍMICA ORGÂNICA, PROTEÍNAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERNARDIM, Barbara et al. Stoichiometric and irreversible cysteine-selective protein modification using carbonylacrylic reagents. Nature Communications, 2016Tradução . . Disponível em: https://doi.org/10.1038/ncomms13128. Acesso em: 28 ago. 2024.
APA
Bernardim, B., Cal, P. M. S. D., Matos, M. J., Oliveira, B. L., Martínez-Sáez, N., Albuquerque, I. S., et al. (2016). Stoichiometric and irreversible cysteine-selective protein modification using carbonylacrylic reagents. Nature Communications. doi:10.1038/ncomms13128
NLM
Bernardim B, Cal PMSD, Matos MJ, Oliveira BL, Martínez-Sáez N, Albuquerque IS, Perkins E, Corzana F, Burtoloso ACB, Jiménez-Osés G, Bernardes GLL. Stoichiometric and irreversible cysteine-selective protein modification using carbonylacrylic reagents [Internet]. Nature Communications. 2016 ;[citado 2024 ago. 28 ] Available from: https://doi.org/10.1038/ncomms13128
Vancouver
Bernardim B, Cal PMSD, Matos MJ, Oliveira BL, Martínez-Sáez N, Albuquerque IS, Perkins E, Corzana F, Burtoloso ACB, Jiménez-Osés G, Bernardes GLL. Stoichiometric and irreversible cysteine-selective protein modification using carbonylacrylic reagents [Internet]. Nature Communications. 2016 ;[citado 2024 ago. 28 ] Available from: https://doi.org/10.1038/ncomms13128

Unidades USP

ReP

Filtros

Tipo de material

Unidades USP

Departamento

Autores

Autores USP

Ano de publicação

Assuntos

Título da fonte

Editora

Nome do evento

Grupo de pesquisa

Agência de fomento

Indexado em

Afiliação dos autores externos normalizada

Afiliação dos autores externos não normalizada

País das instituições de afiliação dos autores externos