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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
Source: Organic Letters. Unidades: IFSC, IQSC
Subjects: SOLUBILIDADE, ESPECTROSCOPIA, POLIMORFISMO
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ABNT
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: 28 abr. 2024.
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 2024 abr. 28 ] 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 2024 abr. 28 ] 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.
Source: Organic Letters. Unidades: ESALQ, IQSC, ICMC
Subjects: ANTÚRIO, BIODIVERSIDADE, COMPOSIÇÃO QUÍMICA, FUNGOS FITOPATOGÊNICOS, METABÓLITOS SECUNDÁRIOS, METABOLÔMICA, MICRORGANISMOS ENDOFÍTICOS
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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: 28 abr. 2024.
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 2024 abr. 28 ] 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 2024 abr. 28 ] 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
Source: Organic Letters. Unidade: IQSC
Subjects: 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: 28 abr. 2024.
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 2024 abr. 28 ] 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 2024 abr. 28 ] 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
Source: Organic Letters. Unidade: IQSC
Subjects: 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: 28 abr. 2024.
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 2024 abr. 28 ] 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 2024 abr. 28 ] 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
Source: Organic Letters. Unidades: FFCLRP, FCFRP
Subjects: 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: 28 abr. 2024.
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 2024 abr. 28 ] 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 2024 abr. 28 ] 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
Source: Organic Letters. Unidade: IQ
Subjects: 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: 28 abr. 2024.
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 2024 abr. 28 ] 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 2024 abr. 28 ] 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
Source: Organic Letters. Unidade: FCFRP
Subjects: 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: 28 abr. 2024.
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 2024 abr. 28 ] 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 2024 abr. 28 ] 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
Source: Organic Letters. Unidade: FCFRP
Subjects: 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: 28 abr. 2024.
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 2024 abr. 28 ] 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 2024 abr. 28 ] 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
Source: Organic Letters. Unidade: IQ
Subjects: 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: 28 abr. 2024.
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 2024 abr. 28 ] 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 2024 abr. 28 ] 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
Source: Organic Letters. Unidades: IQSC, ESALQ
Subjects: 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: 28 abr. 2024.
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 2024 abr. 28 ] 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 2024 abr. 28 ] 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
Source: Organic Letters. Unidades: FFCLRP, FCFRP
Subjects: 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: 28 abr. 2024.
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 2024 abr. 28 ] 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 2024 abr. 28 ] 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
Source: Organic Letters. Unidade: IQ
Subjects: SOLVENTE, ESCHERICHIA COLI
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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: 28 abr. 2024.
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 2024 abr. 28 ] 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 2024 abr. 28 ] 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
Source: Organic Letters. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, REAÇÕES ORGÂNICAS
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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: 28 abr. 2024.
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 2024 abr. 28 ] 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 2024 abr. 28 ] 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
Source: Organic Letters. Unidade: IQSC
Subjects: SÍNTESE QUÍMICA, QUÍMICA ORGÂNICA
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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: 28 abr. 2024.
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 2024 abr. 28 ] 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 2024 abr. 28 ] 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
Source: Organic Letters. Unidade: IQ
Subjects: 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: 28 abr. 2024.
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 2024 abr. 28 ] 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 2024 abr. 28 ] 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
Source: Organic Letters. Unidade: IQ
Subjects: 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: 28 abr. 2024.
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 2024 abr. 28 ] 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 2024 abr. 28 ] 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
Source: Organic Letters. Unidade: FCF
Subjects: 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: 28 abr. 2024.
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 2024 abr. 28 ] 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 2024 abr. 28 ] 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
Source: Organic Letters. Unidade: IQ
Subjects: 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: 28 abr. 2024.
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 2024 abr. 28 ] 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 2024 abr. 28 ] Available from: http://pubs.acs.org/doi/pdf/10.1021/ol8023105
Artigo de periodico
Iodine(III)-promoted ring expansion of 1-vinylcycloalkanol derivatives: a metal-free approach toward seven-membered rings (2008)
Silva Jr., Luiz Fernando da; Vasconcelos, Ramon Sonedson; Nogueira, Mário Augusto
Source: Organic Letters. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, REAGENTES ORGÂNICOS
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA JR., Luiz Fernando da e VASCONCELOS, Ramon Sonedson e NOGUEIRA, Mário Augusto. Iodine(III)-promoted ring expansion of 1-vinylcycloalkanol derivatives: a metal-free approach toward seven-membered rings. Organic Letters, v. 10, n. 5, p. 1017-1020, 2008Tradução . . Acesso em: 28 abr. 2024.
APA
Silva Jr., L. F. da, Vasconcelos, R. S., & Nogueira, M. A. (2008). Iodine(III)-promoted ring expansion of 1-vinylcycloalkanol derivatives: a metal-free approach toward seven-membered rings. Organic Letters, 10( 5), 1017-1020.
NLM
Silva Jr. LF da, Vasconcelos RS, Nogueira MA. Iodine(III)-promoted ring expansion of 1-vinylcycloalkanol derivatives: a metal-free approach toward seven-membered rings. Organic Letters. 2008 ;10( 5): 1017-1020.[citado 2024 abr. 28 ]
Vancouver
Silva Jr. LF da, Vasconcelos RS, Nogueira MA. Iodine(III)-promoted ring expansion of 1-vinylcycloalkanol derivatives: a metal-free approach toward seven-membered rings. Organic Letters. 2008 ;10( 5): 1017-1020.[citado 2024 abr. 28 ]
Artigo de periodico
Iodine(III)-promoted ring contraction of 1,2-dihydronaphthalenes: a diastereoselective total synthesis of (+/-)-indatraline (2007)
Silva Junior, Luiz Fernando da; Siqueira, Fernanda Amaral de; Pedrozo, Eliane Correa; Vieira, Fabiana Yamasaki Martins; Doriguetto, Antonio Carlos
Source: Organic Letters. Unidade: IQ
Subjects: QUÍMICA ORGÂNICA, COCAÍNA, TÁLIO, REAGENTES
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
SILVA JUNIOR, Luiz Fernando da et al. Iodine(III)-promoted ring contraction of 1,2-dihydronaphthalenes: a diastereoselective total synthesis of (+/-)-indatraline. Organic Letters, v. 9, n. 8, p. 1433-1436, 2007Tradução . . Acesso em: 28 abr. 2024.
APA
Silva Junior, L. F. da, Siqueira, F. A. de, Pedrozo, E. C., Vieira, F. Y. M., & Doriguetto, A. C. (2007). Iodine(III)-promoted ring contraction of 1,2-dihydronaphthalenes: a diastereoselective total synthesis of (+/-)-indatraline. Organic Letters, 9( 8), 1433-1436.
NLM
Silva Junior LF da, Siqueira FA de, Pedrozo EC, Vieira FYM, Doriguetto AC. Iodine(III)-promoted ring contraction of 1,2-dihydronaphthalenes: a diastereoselective total synthesis of (+/-)-indatraline. Organic Letters. 2007 ; 9( 8): 1433-1436.[citado 2024 abr. 28 ]
Vancouver
Silva Junior LF da, Siqueira FA de, Pedrozo EC, Vieira FYM, Doriguetto AC. Iodine(III)-promoted ring contraction of 1,2-dihydronaphthalenes: a diastereoselective total synthesis of (+/-)-indatraline. Organic Letters. 2007 ; 9( 8): 1433-1436.[citado 2024 abr. 28 ]

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