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Artigo de periodico
Palladium-catalyzed Carbonylative cyclization of 1-Alkynyl-2-iodo-D-glucal (2024)
Hornink, Milene Macedo ; Figlino, Giuseppe E; Toledo, Mônica Franco Zannini Junqueira ; Pimenta, Daniel Carvalho ; Stefani, Hélio Alexandre
Fonte: Organic Letters. Unidade: FCF
Assuntos: COMPOSTOS AROMÁTICOS, PALÁDIO
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ABNT
HORNINK, Milene Macedo et al. Palladium-catalyzed Carbonylative cyclization of 1-Alkynyl-2-iodo-D-glucal. Organic Letters, v. 26, n. 40, p. 8621−8625, 2024Tradução . . Disponível em: https://dx.doi.org/10.1021/acs.orglett.4c03337. Acesso em: 02 dez. 2025.
APA
Hornink, M. M., Figlino, G. E., Toledo, M. F. Z. J., Pimenta, D. C., & Stefani, H. A. (2024). Palladium-catalyzed Carbonylative cyclization of 1-Alkynyl-2-iodo-D-glucal. Organic Letters, 26( 40), 8621−8625. doi:10.1021/acs.orglett.4c03337
NLM
Hornink MM, Figlino GE, Toledo MFZJ, Pimenta DC, Stefani HA. Palladium-catalyzed Carbonylative cyclization of 1-Alkynyl-2-iodo-D-glucal [Internet]. Organic Letters. 2024 ; 26( 40): 8621−8625.[citado 2025 dez. 02 ] Available from: https://dx.doi.org/10.1021/acs.orglett.4c03337
Vancouver
Hornink MM, Figlino GE, Toledo MFZJ, Pimenta DC, Stefani HA. Palladium-catalyzed Carbonylative cyclization of 1-Alkynyl-2-iodo-D-glucal [Internet]. Organic Letters. 2024 ; 26( 40): 8621−8625.[citado 2025 dez. 02 ] Available from: https://dx.doi.org/10.1021/acs.orglett.4c03337
Artigo de periodico
Synthesis of structural ADP-ribose analogues as inhibitors for SARS-CoV-2 Macrodomain 1 (2024)
Rijpkema, Koen J; Schuller, Marion; Veer, Miriam S. van der; Rieken, Sjoerd; Chang, Diego L. R; Balić, Pascal; Todorov, Alex; Minnee, Hugo; Wijngaarden, Sven; Matos, Isaac A; Hoch, Nicolas Carlos ; Codée, Jeroen D. C ; Ahel, Ivan; Filippov, Dmitri V
Fonte: Organic Letters. Unidade: IQ
Assuntos: COVID-19, ÁCIDOS NUCLEICOS, ADENOSINA TRIFOSFATO
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RIJPKEMA, Koen J et al. Synthesis of structural ADP-ribose analogues as inhibitors for SARS-CoV-2 Macrodomain 1. Organic Letters, v. 26, n. 27, p. 5700−5704, 2024Tradução . . Disponível em: https://dx.doi.org/10.1021/acs.orglett.4c01792. Acesso em: 02 dez. 2025.
APA
Rijpkema, K. J., Schuller, M., Veer, M. S. van der, Rieken, S., Chang, D. L. R., Balić, P., et al. (2024). Synthesis of structural ADP-ribose analogues as inhibitors for SARS-CoV-2 Macrodomain 1. Organic Letters, 26( 27), 5700−5704. doi:10.1021/acs.orglett.4c01792
NLM
Rijpkema KJ, Schuller M, Veer MS van der, Rieken S, Chang DLR, Balić P, Todorov A, Minnee H, Wijngaarden S, Matos IA, Hoch NC, Codée JDC, Ahel I, Filippov DV. Synthesis of structural ADP-ribose analogues as inhibitors for SARS-CoV-2 Macrodomain 1 [Internet]. Organic Letters. 2024 ; 26( 27): 5700−5704.[citado 2025 dez. 02 ] Available from: https://dx.doi.org/10.1021/acs.orglett.4c01792
Vancouver
Rijpkema KJ, Schuller M, Veer MS van der, Rieken S, Chang DLR, Balić P, Todorov A, Minnee H, Wijngaarden S, Matos IA, Hoch NC, Codée JDC, Ahel I, Filippov DV. Synthesis of structural ADP-ribose analogues as inhibitors for SARS-CoV-2 Macrodomain 1 [Internet]. Organic Letters. 2024 ; 26( 27): 5700−5704.[citado 2025 dez. 02 ] Available from: https://dx.doi.org/10.1021/acs.orglett.4c01792
Artigo de periodico
Unveiling a strategy for ring opening of epoxides: synthesis of 2-hydroxyindolinylidenes using α-ester sulfoxonium ylides (2024)
Câmara, Viktor Saraiva; Silva, Aislan Leme da; Luz, Lilian Camargo da; Rodembusch, Fabiano Severo ; Santiago, Pedro Henrique de Oliveira ; Ellena, Javier ; Burtoloso, Antonio Carlos Bender
Fonte: Organic Letters. Unidades: IFSC, IQSC
Assuntos: SOLUBILIDADE, ESPECTROSCOPIA, POLIMORFISMO
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CÂMARA, Viktor Saraiva et al. Unveiling a strategy for ring opening of epoxides: synthesis of 2-hydroxyindolinylidenes using α-ester sulfoxonium ylides. Organic Letters, v. 26, n. Ja 2024, p. 1034-1039 + supporting information: 1-61, 2024Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.3c04169. Acesso em: 02 dez. 2025.
APA
Câmara, V. S., Silva, A. L. da, Luz, L. C. da, Rodembusch, F. S., Santiago, P. H. de O., Ellena, J., & Burtoloso, A. C. B. (2024). Unveiling a strategy for ring opening of epoxides: synthesis of 2-hydroxyindolinylidenes using α-ester sulfoxonium ylides. Organic Letters, 26( Ja 2024), 1034-1039 + supporting information: 1-61. doi:10.1021/acs.orglett.3c04169
NLM
Câmara VS, Silva AL da, Luz LC da, Rodembusch FS, Santiago PH de O, Ellena J, Burtoloso ACB. Unveiling a strategy for ring opening of epoxides: synthesis of 2-hydroxyindolinylidenes using α-ester sulfoxonium ylides [Internet]. Organic Letters. 2024 ; 26( Ja 2024): 1034-1039 + supporting information: 1-61.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.3c04169
Vancouver
Câmara VS, Silva AL da, Luz LC da, Rodembusch FS, Santiago PH de O, Ellena J, Burtoloso ACB. Unveiling a strategy for ring opening of epoxides: synthesis of 2-hydroxyindolinylidenes using α-ester sulfoxonium ylides [Internet]. Organic Letters. 2024 ; 26( Ja 2024): 1034-1039 + supporting information: 1-61.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.3c04169
Artigo de periodico
Metabolomics Reveals a 26-Membered Macrolactone Produced by Endophytic Colletotrichum spp. from Alcatrazes Island, Brazil (2022)
Takaki, Mirelle ; Williams, David E; Freire, Vitor F ; Sartori, Sérgio B; Lira, Simone Possedente de ; Bizarria, Rodolfo; Rodrigues, Andre; Costa, Danielle R. Gonçalves da; Amorim, Marcelo Rodrigues de ; Ferreira, Antonio G; Andersen, Raymond J.
Fonte: Organic Letters. Unidades: ESALQ, IQSC, ICMC
Assuntos: ANTÚRIO, BIODIVERSIDADE, COMPOSIÇÃO QUÍMICA, FUNGOS FITOPATOGÊNICOS, METABÓLITOS SECUNDÁRIOS, METABOLÔMICA, MICRORGANISMOS ENDOFÍTICOS
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ABNT
TAKAKI, Mirelle et al. Metabolomics Reveals a 26-Membered Macrolactone Produced by Endophytic Colletotrichum spp. from Alcatrazes Island, Brazil. Organic Letters, v. 24, n. 51, p. 9381-9385, 2022Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.2c03531. Acesso em: 02 dez. 2025.
APA
Takaki, M., Williams, D. E., Freire, V. F., Sartori, S. B., Lira, S. P. de, Bizarria, R., et al. (2022). Metabolomics Reveals a 26-Membered Macrolactone Produced by Endophytic Colletotrichum spp. from Alcatrazes Island, Brazil. Organic Letters, 24( 51), 9381-9385. doi:10.1021/acs.orglett.2c03531
NLM
Takaki M, Williams DE, Freire VF, Sartori SB, Lira SP de, Bizarria R, Rodrigues A, Costa DRG da, Amorim MR de, Ferreira AG, Andersen RJ. Metabolomics Reveals a 26-Membered Macrolactone Produced by Endophytic Colletotrichum spp. from Alcatrazes Island, Brazil [Internet]. Organic Letters. 2022 ; 24( 51): 9381-9385.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.2c03531
Vancouver
Takaki M, Williams DE, Freire VF, Sartori SB, Lira SP de, Bizarria R, Rodrigues A, Costa DRG da, Amorim MR de, Ferreira AG, Andersen RJ. Metabolomics Reveals a 26-Membered Macrolactone Produced by Endophytic Colletotrichum spp. from Alcatrazes Island, Brazil [Internet]. Organic Letters. 2022 ; 24( 51): 9381-9385.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.2c03531
Artigo de periodico
Visible-Light-Promoted Synthesis of 1,3-Dicarbonyl Sulfoxonium Ylides (2022)
Echemendía, Radell ; Oliveira, Kleber T. de; Burtoloso, Antonio Carlos Bender
Fonte: Organic Letters. Unidade: IQSC
Assuntos: QUÍMICA ORGÂNICA, LUZ, REAÇÕES QUÍMICAS
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ABNT
ECHEMENDÍA, Radell e OLIVEIRA, Kleber T. de e BURTOLOSO, Antonio Carlos Bender. Visible-Light-Promoted Synthesis of 1,3-Dicarbonyl Sulfoxonium Ylides. Organic Letters, v. 24, p. 6386−6390, 2022Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.2c02346. Acesso em: 02 dez. 2025.
APA
Echemendía, R., Oliveira, K. T. de, & Burtoloso, A. C. B. (2022). Visible-Light-Promoted Synthesis of 1,3-Dicarbonyl Sulfoxonium Ylides. Organic Letters, 24, 6386−6390. doi:10.1021/acs.orglett.2c02346
NLM
Echemendía R, Oliveira KT de, Burtoloso ACB. Visible-Light-Promoted Synthesis of 1,3-Dicarbonyl Sulfoxonium Ylides [Internet]. Organic Letters. 2022 ; 24 6386−6390.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.2c02346
Vancouver
Echemendía R, Oliveira KT de, Burtoloso ACB. Visible-Light-Promoted Synthesis of 1,3-Dicarbonyl Sulfoxonium Ylides [Internet]. Organic Letters. 2022 ; 24 6386−6390.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.2c02346
Artigo de periodico
Enantioselective Indole Insertion Reactions of α-Carbonyl Sulfoxonium Ylides (2021)
Leveille, Alexandria N. ; Echemendía, Radell ; Mattson, Anita E ; Burtoloso, Antonio Carlos Bender
Fonte: Organic Letters. Unidade: IQSC
Assuntos: QUÍMICA ORGÂNICA, CATÁLISE
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ABNT
LEVEILLE, Alexandria N. et al. Enantioselective Indole Insertion Reactions of α-Carbonyl Sulfoxonium Ylides. Organic Letters, v. 23, p. 9446−9450, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.1c03627. Acesso em: 02 dez. 2025.
APA
Leveille, A. N., Echemendía, R., Mattson, A. E., & Burtoloso, A. C. B. (2021). Enantioselective Indole Insertion Reactions of α-Carbonyl Sulfoxonium Ylides. Organic Letters, 23, 9446−9450. doi:10.1021/acs.orglett.1c03627
NLM
Leveille AN, Echemendía R, Mattson AE, Burtoloso ACB. Enantioselective Indole Insertion Reactions of α-Carbonyl Sulfoxonium Ylides [Internet]. Organic Letters. 2021 ; 23 9446−9450.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.1c03627
Vancouver
Leveille AN, Echemendía R, Mattson AE, Burtoloso ACB. Enantioselective Indole Insertion Reactions of α-Carbonyl Sulfoxonium Ylides [Internet]. Organic Letters. 2021 ; 23 9446−9450.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.1c03627
Artigo de periodico
Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases (2021)
Santos, Thiago dos ; Orenha, Henrique Pereira; Murie, Valter Eduardo ; Vessecchi, Ricardo ; Clososki, Giuliano Cesar
Fonte: Organic Letters. Unidades: FFCLRP, FCFRP
Assuntos: COMPOSTOS DE NITROGÊNIO, NITRILAS, QUÍMICA ORGÂNICA, COMPOSTOS HETEROCÍCLICOS
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ABNT
SANTOS, Thiago dos et al. Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases. Organic Letters, v. 23, n. 19, p. 7396-7400, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.1c02572. Acesso em: 02 dez. 2025.
APA
Santos, T. dos, Orenha, H. P., Murie, V. E., Vessecchi, R., & Clososki, G. C. (2021). Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases. Organic Letters, 23( 19), 7396-7400. doi:10.1021/acs.orglett.1c02572
NLM
Santos T dos, Orenha HP, Murie VE, Vessecchi R, Clososki GC. Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases [Internet]. Organic Letters. 2021 ; 23( 19): 7396-7400.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.1c02572
Vancouver
Santos T dos, Orenha HP, Murie VE, Vessecchi R, Clososki GC. Selective metalation and functionalization of fluorinated nitriles using 2,2,6,6-tetramethylpiperidyl bases [Internet]. Organic Letters. 2021 ; 23( 19): 7396-7400.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.1c02572
Artigo de periodico
Cascade reactions assisted by microwave irradiation: ultrafast construction of 2-Quinolinone-fused gamma-Lactones from N-(o-Ethynylaryl)acrylamides and formamide (2021)
Sacchelli, Bruce Alan Lobo ; Rocha, Bianca Campanile; Andrade, Leandro Helgueira
Fonte: Organic Letters. Unidade: IQ
Assuntos: PERÓXIDO DE HIDROGÊNIO, IRRADIAÇÃO, TECNOLOGIA DE MICRO-ONDAS
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ABNT
SACCHELLI, Bruce Alan Lobo e ROCHA, Bianca Campanile e ANDRADE, Leandro Helgueira. Cascade reactions assisted by microwave irradiation: ultrafast construction of 2-Quinolinone-fused gamma-Lactones from N-(o-Ethynylaryl)acrylamides and formamide. Organic Letters, v. 23, n. 13, p. 5071–5075, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.1c01606. Acesso em: 02 dez. 2025.
APA
Sacchelli, B. A. L., Rocha, B. C., & Andrade, L. H. (2021). Cascade reactions assisted by microwave irradiation: ultrafast construction of 2-Quinolinone-fused gamma-Lactones from N-(o-Ethynylaryl)acrylamides and formamide. Organic Letters, 23( 13), 5071–5075. doi:10.1021/acs.orglett.1c01606
NLM
Sacchelli BAL, Rocha BC, Andrade LH. Cascade reactions assisted by microwave irradiation: ultrafast construction of 2-Quinolinone-fused gamma-Lactones from N-(o-Ethynylaryl)acrylamides and formamide [Internet]. Organic Letters. 2021 ; 23( 13): 5071–5075.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.1c01606
Vancouver
Sacchelli BAL, Rocha BC, Andrade LH. Cascade reactions assisted by microwave irradiation: ultrafast construction of 2-Quinolinone-fused gamma-Lactones from N-(o-Ethynylaryl)acrylamides and formamide [Internet]. Organic Letters. 2021 ; 23( 13): 5071–5075.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.1c01606
Artigo de periodico
Chemical exchanges between multilateral symbionts (2021)
Bae, Munhyung; Mevers, Emily; Pishchany, Gleb; Whaley, Sarah G.; Rock, Charles O.; Andes, David R.; Currie, Cameron R.; Pupo, Monica Tallarico ; Clardy, Jon
Fonte: Organic Letters. Unidade: FCFRP
Assuntos: MOLÉCULA, ECOLOGIA QUÍMICA, FORMIGAS, FUNGOS, SIMBIOSE
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ABNT
BAE, Munhyung et al. Chemical exchanges between multilateral symbionts. Organic Letters, v. 23, n. 5, p. 1648-1652, 2021Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.1c00068. Acesso em: 02 dez. 2025.
APA
Bae, M., Mevers, E., Pishchany, G., Whaley, S. G., Rock, C. O., Andes, D. R., et al. (2021). Chemical exchanges between multilateral symbionts. Organic Letters, 23( 5), 1648-1652. doi:10.1021/acs.orglett.1c00068
NLM
Bae M, Mevers E, Pishchany G, Whaley SG, Rock CO, Andes DR, Currie CR, Pupo MT, Clardy J. Chemical exchanges between multilateral symbionts [Internet]. Organic Letters. 2021 ; 23( 5): 1648-1652.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.1c00068
Vancouver
Bae M, Mevers E, Pishchany G, Whaley SG, Rock CO, Andes DR, Currie CR, Pupo MT, Clardy J. Chemical exchanges between multilateral symbionts [Internet]. Organic Letters. 2021 ; 23( 5): 1648-1652.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.1c00068
Artigo de periodico
Copper reactivity can be tuned to catalyze the stereoselective synthesis of 2-deoxyglycosides from glycals (2020)
Palo-Nieto, Carlos; Sau, Abhijit; Jeanneret, Robin; Payard, Pierre-Adrien; Salamé, Aude; Teixeira, Maristela Braga; Carvalho, Ivone ; Grimaud, Laurence; Galan, M. Carmen
Fonte: Organic Letters. Unidade: FCFRP
Assuntos: COBRE, CATÁLISE, QUÍMICA ORGÂNICA, CARBOIDRATOS
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ABNT
PALO-NIETO, Carlos et al. Copper reactivity can be tuned to catalyze the stereoselective synthesis of 2-deoxyglycosides from glycals. Organic Letters, v. 22, n. 5, p. 1991-1996, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.9b04525. Acesso em: 02 dez. 2025.
APA
Palo-Nieto, C., Sau, A., Jeanneret, R., Payard, P. -A., Salamé, A., Teixeira, M. B., et al. (2020). Copper reactivity can be tuned to catalyze the stereoselective synthesis of 2-deoxyglycosides from glycals. Organic Letters, 22( 5), 1991-1996. doi:10.1021/acs.orglett.9b04525
NLM
Palo-Nieto C, Sau A, Jeanneret R, Payard P-A, Salamé A, Teixeira MB, Carvalho I, Grimaud L, Galan MC. Copper reactivity can be tuned to catalyze the stereoselective synthesis of 2-deoxyglycosides from glycals [Internet]. Organic Letters. 2020 ; 22( 5): 1991-1996.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.9b04525
Vancouver
Palo-Nieto C, Sau A, Jeanneret R, Payard P-A, Salamé A, Teixeira MB, Carvalho I, Grimaud L, Galan MC. Copper reactivity can be tuned to catalyze the stereoselective synthesis of 2-deoxyglycosides from glycals [Internet]. Organic Letters. 2020 ; 22( 5): 1991-1996.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.9b04525
Artigo de periodico
Iron-catalyzed synthesis of oxindoles: application to the preparation of pyrroloindolines (2017)
Correia, Valquírio G; Abreu, Juliana C; Barata, Caio A. E; Andrade, Leandro Helgueira
Fonte: Organic Letters. Unidade: IQ
Assuntos: SÍNTESE ORGÂNICA, ALCALOIDES DE PIRROLIZIDINA
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ABNT
CORREIA, Valquírio G et al. Iron-catalyzed synthesis of oxindoles: application to the preparation of pyrroloindolines. Organic Letters, v. 19, n. 5, p. 1060-1063, 2017Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.7b00078. Acesso em: 02 dez. 2025.
APA
Correia, V. G., Abreu, J. C., Barata, C. A. E., & Andrade, L. H. (2017). Iron-catalyzed synthesis of oxindoles: application to the preparation of pyrroloindolines. Organic Letters, 19( 5), 1060-1063. doi:10.1021/acs.orglett.7b00078
NLM
Correia VG, Abreu JC, Barata CAE, Andrade LH. Iron-catalyzed synthesis of oxindoles: application to the preparation of pyrroloindolines [Internet]. Organic Letters. 2017 ; 19( 5): 1060-1063.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.7b00078
Vancouver
Correia VG, Abreu JC, Barata CAE, Andrade LH. Iron-catalyzed synthesis of oxindoles: application to the preparation of pyrroloindolines [Internet]. Organic Letters. 2017 ; 19( 5): 1060-1063.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.7b00078
Artigo de periodico
Structure and biogenesis of Roussoellatide, a Dichlorinated polyketide from the marine-derived fungs Roussoella sp DLM33 (2015)
Ferreira, Ewerton Lucena F; Williams, David E; Ióca, Laura Pavan; Morais-Urano, Raquel P; Santos, Mario Ferreira Conceição; Patrick, Brian o; Elias, Luciana Mecatti; Lira, Simone P; Ferreira, Antonio Geraldo; Passarini, Michel Rodrigo Zambrano; Sette, Lara D; Andersen, Raymond J; Berlinck, Roberto Gomes de Souza
Fonte: Organic Letters. Unidades: IQSC, ESALQ
Assuntos: FUNGOS (ESTRUTURA), METABÓLITOS SECUNDÁRIOS
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ABNT
FERREIRA, Ewerton Lucena F et al. Structure and biogenesis of Roussoellatide, a Dichlorinated polyketide from the marine-derived fungs Roussoella sp DLM33. Organic Letters, v. 17, p. 5152-5155, 2015Tradução . . Disponível em: https://doi.org/10.1021/acs.orglett.5b02060. Acesso em: 02 dez. 2025.
APA
Ferreira, E. L. F., Williams, D. E., Ióca, L. P., Morais-Urano, R. P., Santos, M. F. C., Patrick, B. o, et al. (2015). Structure and biogenesis of Roussoellatide, a Dichlorinated polyketide from the marine-derived fungs Roussoella sp DLM33. Organic Letters, 17, 5152-5155. doi:10.1021/acs.orglett.5b02060
NLM
Ferreira ELF, Williams DE, Ióca LP, Morais-Urano RP, Santos MFC, Patrick B o, Elias LM, Lira SP, Ferreira AG, Passarini MRZ, Sette LD, Andersen RJ, Berlinck RG de S. Structure and biogenesis of Roussoellatide, a Dichlorinated polyketide from the marine-derived fungs Roussoella sp DLM33 [Internet]. Organic Letters. 2015 ; 17 5152-5155.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.5b02060
Vancouver
Ferreira ELF, Williams DE, Ióca LP, Morais-Urano RP, Santos MFC, Patrick B o, Elias LM, Lira SP, Ferreira AG, Passarini MRZ, Sette LD, Andersen RJ, Berlinck RG de S. Structure and biogenesis of Roussoellatide, a Dichlorinated polyketide from the marine-derived fungs Roussoella sp DLM33 [Internet]. Organic Letters. 2015 ; 17 5152-5155.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/acs.orglett.5b02060
Artigo de periodico
Directed metalation of 1-ester-substituted indolizines: base/electrophile-controlled regioselective functionalization (2015)
Amaral, Mônica F. Z. J.; Baumgartner, Amanda A.; Vessecchi, Ricardo; Clososki, Giuliano Cesar
Fonte: Organic Letters. Unidades: FFCLRP, FCFRP
Assuntos: SÍNTESE ORGÂNICA, QUÍMICA ORGÂNICA
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ABNT
AMARAL, Mônica F. Z. J. et al. Directed metalation of 1-ester-substituted indolizines: base/electrophile-controlled regioselective functionalization. Organic Letters, v. 17, n. 2, p. 238–241, 2015Tradução . . Disponível em: https://doi.org/10.1021/ol503288e. Acesso em: 02 dez. 2025.
APA
Amaral, M. F. Z. J., Baumgartner, A. A., Vessecchi, R., & Clososki, G. C. (2015). Directed metalation of 1-ester-substituted indolizines: base/electrophile-controlled regioselective functionalization. Organic Letters, 17( 2), 238–241. doi:10.1021/ol503288e
NLM
Amaral MFZJ, Baumgartner AA, Vessecchi R, Clososki GC. Directed metalation of 1-ester-substituted indolizines: base/electrophile-controlled regioselective functionalization [Internet]. Organic Letters. 2015 ; 17( 2): 238–241.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/ol503288e
Vancouver
Amaral MFZJ, Baumgartner AA, Vessecchi R, Clososki GC. Directed metalation of 1-ester-substituted indolizines: base/electrophile-controlled regioselective functionalization [Internet]. Organic Letters. 2015 ; 17( 2): 238–241.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/ol503288e
Artigo de periodico
Continuous flow synthesis of chiral amines in organic solvents: immobilization of E. coli cells containing both ω-transaminase and PLP (2014)
Andrade, Leandro Helgueira ; Kroutil, Wolgang; Jamison, Timothy F
Fonte: Organic Letters. Unidade: IQ
Assuntos: SOLVENTE, ESCHERICHIA COLI
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ANDRADE, Leandro Helgueira e KROUTIL, Wolgang e JAMISON, Timothy F. Continuous flow synthesis of chiral amines in organic solvents: immobilization of E. coli cells containing both ω-transaminase and PLP. Organic Letters, v. 16, n. 23, p. 6092-6095, 2014Tradução . . Disponível em: https://doi.org/10.1021/ol502712v. Acesso em: 02 dez. 2025.
APA
Andrade, L. H., Kroutil, W., & Jamison, T. F. (2014). Continuous flow synthesis of chiral amines in organic solvents: immobilization of E. coli cells containing both ω-transaminase and PLP. Organic Letters, 16( 23), 6092-6095. doi:10.1021/ol502712v
NLM
Andrade LH, Kroutil W, Jamison TF. Continuous flow synthesis of chiral amines in organic solvents: immobilization of E. coli cells containing both ω-transaminase and PLP [Internet]. Organic Letters. 2014 ; 16( 23): 6092-6095.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/ol502712v
Vancouver
Andrade LH, Kroutil W, Jamison TF. Continuous flow synthesis of chiral amines in organic solvents: immobilization of E. coli cells containing both ω-transaminase and PLP [Internet]. Organic Letters. 2014 ; 16( 23): 6092-6095.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/ol502712v
Artigo de periodico
Synthesis and diels-alder reactions of a benzo[5]radialene derivative (2014)
Richthofen, Andreas Albert Von; Marzorati, Liliana ; Ducati, Lucas Colucci ; Di Vitta, Cláudio
Fonte: Organic Letters. Unidade: IQ
Assuntos: QUÍMICA ORGÂNICA, REAÇÕES ORGÂNICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
RICHTHOFEN, Andreas Albert Von et al. Synthesis and diels-alder reactions of a benzo[5]radialene derivative. Organic Letters, v. 16, n. 15, p. 4020-4023, 2014Tradução . . Disponível em: https://doi.org/10.1021/ol5018432. Acesso em: 02 dez. 2025.
APA
Richthofen, A. A. V., Marzorati, L., Ducati, L. C., & Di Vitta, C. (2014). Synthesis and diels-alder reactions of a benzo[5]radialene derivative. Organic Letters, 16( 15), 4020-4023. doi:10.1021/ol5018432
NLM
Richthofen AAV, Marzorati L, Ducati LC, Di Vitta C. Synthesis and diels-alder reactions of a benzo[5]radialene derivative [Internet]. Organic Letters. 2014 ; 16( 15): 4020-4023.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/ol5018432
Vancouver
Richthofen AAV, Marzorati L, Ducati LC, Di Vitta C. Synthesis and diels-alder reactions of a benzo[5]radialene derivative [Internet]. Organic Letters. 2014 ; 16( 15): 4020-4023.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/ol5018432
Artigo de periodico
SmI2‑mediated couplings of a‑amino acid derivatives: formal synthesis of (-)-pumiliotoxin 251D and (+/-)-epiquinamide (2013)
Pinho, Vagner Dantas; Procter, David J.; Burtoloso, Antonio Carlos Bender
Fonte: Organic Letters. Unidade: IQSC
Assuntos: SÍNTESE QUÍMICA, QUÍMICA ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
PINHO, Vagner Dantas e PROCTER, David J. e BURTOLOSO, Antonio Carlos Bender. SmI2‑mediated couplings of a‑amino acid derivatives: formal synthesis of (-)-pumiliotoxin 251D and (+/-)-epiquinamide. Organic Letters, v. 15, n. 10, p. 2434-2437, 2013Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/ol400903n. Acesso em: 02 dez. 2025.
APA
Pinho, V. D., Procter, D. J., & Burtoloso, A. C. B. (2013). SmI2‑mediated couplings of a‑amino acid derivatives: formal synthesis of (-)-pumiliotoxin 251D and (+/-)-epiquinamide. Organic Letters, 15( 10), 2434-2437. doi:10.1021/ol400903n
NLM
Pinho VD, Procter DJ, Burtoloso ACB. SmI2‑mediated couplings of a‑amino acid derivatives: formal synthesis of (-)-pumiliotoxin 251D and (+/-)-epiquinamide [Internet]. Organic Letters. 2013 ; 15( 10): 2434-2437.[citado 2025 dez. 02 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/ol400903n
Vancouver
Pinho VD, Procter DJ, Burtoloso ACB. SmI2‑mediated couplings of a‑amino acid derivatives: formal synthesis of (-)-pumiliotoxin 251D and (+/-)-epiquinamide [Internet]. Organic Letters. 2013 ; 15( 10): 2434-2437.[citado 2025 dez. 02 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/ol400903n
Artigo de periodico
Room temperature, metal-free synthesis of diaryl ethers with use of diaryliodonium salts (2011)
Jalalian, Nazli; Ishikawa, Eloisa Erika; Silva Junior, Luiz Fernando da; Olofsson, Berit
Fonte: Organic Letters. Unidade: IQ
Assuntos: PRODUTOS NATURAIS, QUÍMICA ORGÂNICA, IODO
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
JALALIAN, Nazli et al. Room temperature, metal-free synthesis of diaryl ethers with use of diaryliodonium salts. Organic Letters, v. 13, n. 6, p. 1552-1555, 2011Tradução . . Disponível em: https://doi.org/10.1021/ol200265t. Acesso em: 02 dez. 2025.
APA
Jalalian, N., Ishikawa, E. E., Silva Junior, L. F. da, & Olofsson, B. (2011). Room temperature, metal-free synthesis of diaryl ethers with use of diaryliodonium salts. Organic Letters, 13( 6), 1552-1555. doi:10.1021/ol200265t
NLM
Jalalian N, Ishikawa EE, Silva Junior LF da, Olofsson B. Room temperature, metal-free synthesis of diaryl ethers with use of diaryliodonium salts [Internet]. Organic Letters. 2011 ; 13( 6): 1552-1555.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/ol200265t
Vancouver
Jalalian N, Ishikawa EE, Silva Junior LF da, Olofsson B. Room temperature, metal-free synthesis of diaryl ethers with use of diaryliodonium salts [Internet]. Organic Letters. 2011 ; 13( 6): 1552-1555.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/ol200265t
Artigo de periodico
Lipase-catalyzed highly enantioselective kinetic resolution of boron-containing chiral alcohols (2009)
Andrade, Leandro Helgueira ; Barcellos, Thiago
Fonte: Organic Letters. Unidade: IQ
Assuntos: LIPASE, REAÇÕES ORGÂNICAS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
ANDRADE, Leandro Helgueira e BARCELLOS, Thiago. Lipase-catalyzed highly enantioselective kinetic resolution of boron-containing chiral alcohols. Organic Letters, v. 11, n. 14, p. 3052-3055, 2009Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/ol901091f. Acesso em: 02 dez. 2025.
APA
Andrade, L. H., & Barcellos, T. (2009). Lipase-catalyzed highly enantioselective kinetic resolution of boron-containing chiral alcohols. Organic Letters, 11( 14), 3052-3055. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/ol901091f
NLM
Andrade LH, Barcellos T. Lipase-catalyzed highly enantioselective kinetic resolution of boron-containing chiral alcohols [Internet]. Organic Letters. 2009 ; 11( 14): 3052-3055.[citado 2025 dez. 02 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/ol901091f
Vancouver
Andrade LH, Barcellos T. Lipase-catalyzed highly enantioselective kinetic resolution of boron-containing chiral alcohols [Internet]. Organic Letters. 2009 ; 11( 14): 3052-3055.[citado 2025 dez. 02 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/ol901091f
Artigo de periodico
Nucleophilic addition of potassium alkynyltrifluoroborates to d-glucal mediated by B'F IND. 3´`PONTO´O`Et IND. 2´: Highly stereoselective synthesis of α-C-glycosides (2008)
Vieira, Adriano Siqueira; Fiorante, Pedro de Freitas; Hough, Thomas L. S; Ferreira, Fernando P; Lüdtke, Diogo, Seibert; Stefani, Hélio Alexandre
Fonte: Organic Letters. Unidade: FCF
Assuntos: POTÁSSIO, SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
VIEIRA, Adriano Siqueira et al. Nucleophilic addition of potassium alkynyltrifluoroborates to d-glucal mediated by B'F IND. 3´`PONTO´O`Et IND. 2´: Highly stereoselective synthesis of α-C-glycosides. Organic Letters, v. 10, n. 22, p. 5215-5218, 2008Tradução . . Disponível em: https://doi.org/10.1021/ol8022177. Acesso em: 02 dez. 2025.
APA
Vieira, A. S., Fiorante, P. de F., Hough, T. L. S., Ferreira, F. P., Lüdtke, D., & Stefani, H. A. (2008). Nucleophilic addition of potassium alkynyltrifluoroborates to d-glucal mediated by B'F IND. 3´`PONTO´O`Et IND. 2´: Highly stereoselective synthesis of α-C-glycosides. Organic Letters, 10( 22), 5215-5218. doi:10.1021/ol8022177
NLM
Vieira AS, Fiorante P de F, Hough TLS, Ferreira FP, Lüdtke D, Stefani HA. Nucleophilic addition of potassium alkynyltrifluoroborates to d-glucal mediated by B'F IND. 3´`PONTO´O`Et IND. 2´: Highly stereoselective synthesis of α-C-glycosides [Internet]. Organic Letters. 2008 ; 10( 22): 5215-5218.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/ol8022177
Vancouver
Vieira AS, Fiorante P de F, Hough TLS, Ferreira FP, Lüdtke D, Stefani HA. Nucleophilic addition of potassium alkynyltrifluoroborates to d-glucal mediated by B'F IND. 3´`PONTO´O`Et IND. 2´: Highly stereoselective synthesis of α-C-glycosides [Internet]. Organic Letters. 2008 ; 10( 22): 5215-5218.[citado 2025 dez. 02 ] Available from: https://doi.org/10.1021/ol8022177
Artigo de periodico
A diastereoselective total synthesis of trans-trikentrin A: a ring contraction approach (2008)
Silva Jr., Luiz Fernando da; Craveiro, Marcus Vinicius
Fonte: Organic Letters. Unidade: IQ
Assuntos: TÁLIO, REAGENTES ORGÂNICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA JR., Luiz Fernando da e CRAVEIRO, Marcus Vinicius. A diastereoselective total synthesis of trans-trikentrin A: a ring contraction approach. Organic Letters, v. 10, n. 23, p. 5417-5420, 2008Tradução . . Disponível em: http://pubs.acs.org/doi/pdf/10.1021/ol8023105. Acesso em: 02 dez. 2025.
APA
Silva Jr., L. F. da, & Craveiro, M. V. (2008). A diastereoselective total synthesis of trans-trikentrin A: a ring contraction approach. Organic Letters, 10( 23), 5417-5420. Recuperado de http://pubs.acs.org/doi/pdf/10.1021/ol8023105
NLM
Silva Jr. LF da, Craveiro MV. A diastereoselective total synthesis of trans-trikentrin A: a ring contraction approach [Internet]. Organic Letters. 2008 ; 10( 23): 5417-5420.[citado 2025 dez. 02 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/ol8023105
Vancouver
Silva Jr. LF da, Craveiro MV. A diastereoselective total synthesis of trans-trikentrin A: a ring contraction approach [Internet]. Organic Letters. 2008 ; 10( 23): 5417-5420.[citado 2025 dez. 02 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/ol8023105

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