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Artigo de periodico
Precise Installation of Diazo-Tagged Side-Chains on Proteins to Enable In Vitro and In-Cell Site-Specific Labeling (2020)
Bernardim, Barbara ; Dunsmore, Lavinia ; Li, He; Hocking, Brad; Nuñez-Franco, Reyes; Navo, Claudio D. ; Jiménez-Osés, Gonzalo ; Burtoloso, Antonio Carlos Bender ; Bernardes, Gonçalo J. L.
Source: Bioconjugate Chemistry. Unidade: IQSC
Subjects: SÍNTESE ORGÂNICA, REAGENTES, PROTEÍNAS, ANTICORPOS
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ABNT
BERNARDIM, Barbara et al. Precise Installation of Diazo-Tagged Side-Chains on Proteins to Enable In Vitro and In-Cell Site-Specific Labeling. Bioconjugate Chemistry, v. 31, n. 6, p. 1604-1610 June 2020, 2020Tradução . . Disponível em: https://doi.org/10.1021/acs.bioconjchem.0c00232. Acesso em: 09 out. 2025.
APA
Bernardim, B., Dunsmore, L., Li, H., Hocking, B., Nuñez-Franco, R., Navo, C. D., et al. (2020). Precise Installation of Diazo-Tagged Side-Chains on Proteins to Enable In Vitro and In-Cell Site-Specific Labeling. Bioconjugate Chemistry, 31( 6), 1604-1610 June 2020. doi:10.1021/acs.bioconjchem.0c00232
NLM
Bernardim B, Dunsmore L, Li H, Hocking B, Nuñez-Franco R, Navo CD, Jiménez-Osés G, Burtoloso ACB, Bernardes GJL. Precise Installation of Diazo-Tagged Side-Chains on Proteins to Enable In Vitro and In-Cell Site-Specific Labeling [Internet]. Bioconjugate Chemistry. 2020 ; 31( 6): 1604-1610 June 2020.[citado 2025 out. 09 ] Available from: https://doi.org/10.1021/acs.bioconjchem.0c00232
Vancouver
Bernardim B, Dunsmore L, Li H, Hocking B, Nuñez-Franco R, Navo CD, Jiménez-Osés G, Burtoloso ACB, Bernardes GJL. Precise Installation of Diazo-Tagged Side-Chains on Proteins to Enable In Vitro and In-Cell Site-Specific Labeling [Internet]. Bioconjugate Chemistry. 2020 ; 31( 6): 1604-1610 June 2020.[citado 2025 out. 09 ] Available from: https://doi.org/10.1021/acs.bioconjchem.0c00232
Artigo de periodico
Efficient and irreversible antibody–cysteine bioconjugation using carbonylacrylic reagents (2019)
Bernardim, Barbara; Matos, Maria J; Ferhati, Xhenti; Compañón, Ismael; Guerreiro, Ana; Akkapeddi, Padma; Burtoloso, Antonio Carlos Bender ; Jiménez-Osés, Gonzalo; Corzana, Francisco; Bernardes, Gonçalo J. L
Source: Nature Protocols. Unidade: IQSC
Subjects: QUÍMICA ORGÂNICA, SÍNTESE ORGÂNICA
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ABNT
BERNARDIM, Barbara et al. Efficient and irreversible antibody–cysteine bioconjugation using carbonylacrylic reagents. Nature Protocols, v. 14, n. Ja 2019, p. 86-99, 2019Tradução . . Disponível em: https://doi.org/10.1038/s41596-018-0083-9. Acesso em: 09 out. 2025.
APA
Bernardim, B., Matos, M. J., Ferhati, X., Compañón, I., Guerreiro, A., Akkapeddi, P., et al. (2019). Efficient and irreversible antibody–cysteine bioconjugation using carbonylacrylic reagents. Nature Protocols, 14( Ja 2019), 86-99. doi:10.1038/s41596-018-0083-9
NLM
Bernardim B, Matos MJ, Ferhati X, Compañón I, Guerreiro A, Akkapeddi P, Burtoloso ACB, Jiménez-Osés G, Corzana F, Bernardes GJL. Efficient and irreversible antibody–cysteine bioconjugation using carbonylacrylic reagents [Internet]. Nature Protocols. 2019 ; 14( Ja 2019): 86-99.[citado 2025 out. 09 ] Available from: https://doi.org/10.1038/s41596-018-0083-9
Vancouver
Bernardim B, Matos MJ, Ferhati X, Compañón I, Guerreiro A, Akkapeddi P, Burtoloso ACB, Jiménez-Osés G, Corzana F, Bernardes GJL. Efficient and irreversible antibody–cysteine bioconjugation using carbonylacrylic reagents [Internet]. Nature Protocols. 2019 ; 14( Ja 2019): 86-99.[citado 2025 out. 09 ] Available from: https://doi.org/10.1038/s41596-018-0083-9
Trabalho de evento-resumo
Alfa, Beta-Unsaturated diazoketones as substrates for intramolecular [2+2] and [4+2] cycloadditions (2017)
Bernardim, Barbara; Burtoloso, Antonio Carlos Bender
Source: Proceedings. Conference titles: IUPAC General Assembly. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
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ABNT
BERNARDIM, Barbara e BURTOLOSO, Antonio Carlos Bender. Alfa, Beta-Unsaturated diazoketones as substrates for intramolecular [2+2] and [4+2] cycloadditions. 2017, Anais.. Durham: IUPAC, 2017. Disponível em: https://repositorio.usp.br/directbitstream/5acd0c96-4ed3-461e-9961-21a205154e56/P16980.pdf. Acesso em: 09 out. 2025.
APA
Bernardim, B., & Burtoloso, A. C. B. (2017). Alfa, Beta-Unsaturated diazoketones as substrates for intramolecular [2+2] and [4+2] cycloadditions. In Proceedings. Durham: IUPAC. Recuperado de https://repositorio.usp.br/directbitstream/5acd0c96-4ed3-461e-9961-21a205154e56/P16980.pdf
NLM
Bernardim B, Burtoloso ACB. Alfa, Beta-Unsaturated diazoketones as substrates for intramolecular [2+2] and [4+2] cycloadditions [Internet]. Proceedings. 2017 ;[citado 2025 out. 09 ] Available from: https://repositorio.usp.br/directbitstream/5acd0c96-4ed3-461e-9961-21a205154e56/P16980.pdf
Vancouver
Bernardim B, Burtoloso ACB. Alfa, Beta-Unsaturated diazoketones as substrates for intramolecular [2+2] and [4+2] cycloadditions [Internet]. Proceedings. 2017 ;[citado 2025 out. 09 ] Available from: https://repositorio.usp.br/directbitstream/5acd0c96-4ed3-461e-9961-21a205154e56/P16980.pdf
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.
Source: Nature Communications. Unidade: IQSC
Subjects: QUÍMICA ORGÂNICA, PROTEÍNAS
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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: 09 out. 2025.
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 2025 out. 09 ] 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 2025 out. 09 ] Available from: https://doi.org/10.1038/ncomms13128
Artigo de periodico
Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds (2016)
Bernardim, Barbara; Couch, Erica D.; Hardman-Baldwin, Andrea M; Burtoloso, Antonio Carlos Bender ; Mattson, Anitta E
Source: Synthesis. Unidade: IQSC
Subjects: SÍNTESE ORGÂNICA, UREIA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERNARDIM, Barbara et al. Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds. Synthesis, v. 48, n. 5, p. 677-686, 2016Tradução . . Disponível em: https://doi.org/10.1055/s-0035-1561061. Acesso em: 09 out. 2025.
APA
Bernardim, B., Couch, E. D., Hardman-Baldwin, A. M., Burtoloso, A. C. B., & Mattson, A. E. (2016). Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds. Synthesis, 48( 5), 677-686. doi:10.1055/s-0035-1561061
NLM
Bernardim B, Couch ED, Hardman-Baldwin AM, Burtoloso ACB, Mattson AE. Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds [Internet]. Synthesis. 2016 ; 48( 5): 677-686.[citado 2025 out. 09 ] Available from: https://doi.org/10.1055/s-0035-1561061
Vancouver
Bernardim B, Couch ED, Hardman-Baldwin AM, Burtoloso ACB, Mattson AE. Divergent roles of urea and phosphoric acid derived catalysts in reactions of diazo compounds [Internet]. Synthesis. 2016 ; 48( 5): 677-686.[citado 2025 out. 09 ] Available from: https://doi.org/10.1055/s-0035-1561061
Artigo de periodico
LED lighting as a simple, inexpensive, and sustainable alternative for Wolff rearrangements (2015)
Bernardim, Barbara; Hardman-Baldwin, Andrea M; Burtoloso, Antonio Carlos Bender
Source: RSC Advances. Unidade: IQSC
Assunto: QUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERNARDIM, Barbara e HARDMAN-BALDWIN, Andrea M e BURTOLOSO, Antonio Carlos Bender. LED lighting as a simple, inexpensive, and sustainable alternative for Wolff rearrangements. RSC Advances, v. 5, n. 18, p. 13311-13314, 2015Tradução . . Disponível em: https://doi.org/10.1039/c4ra15670f. Acesso em: 09 out. 2025.
APA
Bernardim, B., Hardman-Baldwin, A. M., & Burtoloso, A. C. B. (2015). LED lighting as a simple, inexpensive, and sustainable alternative for Wolff rearrangements. RSC Advances, 5( 18), 13311-13314. doi:10.1039/c4ra15670f
NLM
Bernardim B, Hardman-Baldwin AM, Burtoloso ACB. LED lighting as a simple, inexpensive, and sustainable alternative for Wolff rearrangements [Internet]. RSC Advances. 2015 ; 5( 18): 13311-13314.[citado 2025 out. 09 ] Available from: https://doi.org/10.1039/c4ra15670f
Vancouver
Bernardim B, Hardman-Baldwin AM, Burtoloso ACB. LED lighting as a simple, inexpensive, and sustainable alternative for Wolff rearrangements [Internet]. RSC Advances. 2015 ; 5( 18): 13311-13314.[citado 2025 out. 09 ] Available from: https://doi.org/10.1039/c4ra15670f
Artigo de periodico
Advances in the enantioselective metal-catalyzed N-H and O-H insertion reactions with diazocarbonyl compounds (2015)
Burtoloso, Antonio Carlos Bender ; Santiago, João V.; Bernardim, Barbara; Talero, Alexánder G.
Source: Current Organic Synthesis. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
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ABNT
BURTOLOSO, Antonio Carlos Bender et al. Advances in the enantioselective metal-catalyzed N-H and O-H insertion reactions with diazocarbonyl compounds. Current Organic Synthesis, v. 12, n. 5, p. 650-659, 2015Tradução . . Disponível em: https://doi.org/10.2174/157017941205150821153658. Acesso em: 09 out. 2025.
APA
Burtoloso, A. C. B., Santiago, J. V., Bernardim, B., & Talero, A. G. (2015). Advances in the enantioselective metal-catalyzed N-H and O-H insertion reactions with diazocarbonyl compounds. Current Organic Synthesis, 12( 5), 650-659. doi:10.2174/157017941205150821153658
NLM
Burtoloso ACB, Santiago JV, Bernardim B, Talero AG. Advances in the enantioselective metal-catalyzed N-H and O-H insertion reactions with diazocarbonyl compounds [Internet]. Current Organic Synthesis. 2015 ; 12( 5): 650-659.[citado 2025 out. 09 ] Available from: https://doi.org/10.2174/157017941205150821153658
Vancouver
Burtoloso ACB, Santiago JV, Bernardim B, Talero AG. Advances in the enantioselective metal-catalyzed N-H and O-H insertion reactions with diazocarbonyl compounds [Internet]. Current Organic Synthesis. 2015 ; 12( 5): 650-659.[citado 2025 out. 09 ] Available from: https://doi.org/10.2174/157017941205150821153658
Artigo de periodico
Alpha-beta-Unsaturated Diazoketones as Useful Platforms in the Synthesis of Nitrogen Heterocycles (2015)
Burtoloso, Antonio Carlos Bender ; Dias, Rafael Mafra de Paula; Bernardim, Barbara
Source: Accounts of Chemical Research. Unidade: IQSC
Assunto: SÍNTESE QUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BURTOLOSO, Antonio Carlos Bender e DIAS, Rafael Mafra de Paula e BERNARDIM, Barbara. Alpha-beta-Unsaturated Diazoketones as Useful Platforms in the Synthesis of Nitrogen Heterocycles. Accounts of Chemical Research, v. 48, n. 4, p. 921-934, 2015Tradução . . Disponível em: https://doi.org/10.1021/ar500433t. Acesso em: 09 out. 2025.
APA
Burtoloso, A. C. B., Dias, R. M. de P., & Bernardim, B. (2015). Alpha-beta-Unsaturated Diazoketones as Useful Platforms in the Synthesis of Nitrogen Heterocycles. Accounts of Chemical Research, 48( 4), 921-934. doi:10.1021/ar500433t
NLM
Burtoloso ACB, Dias RM de P, Bernardim B. Alpha-beta-Unsaturated Diazoketones as Useful Platforms in the Synthesis of Nitrogen Heterocycles [Internet]. Accounts of Chemical Research. 2015 ; 48( 4): 921-934.[citado 2025 out. 09 ] Available from: https://doi.org/10.1021/ar500433t
Vancouver
Burtoloso ACB, Dias RM de P, Bernardim B. Alpha-beta-Unsaturated Diazoketones as Useful Platforms in the Synthesis of Nitrogen Heterocycles [Internet]. Accounts of Chemical Research. 2015 ; 48( 4): 921-934.[citado 2025 out. 09 ] Available from: https://doi.org/10.1021/ar500433t
Artigo de periodico
A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal (2014)
Bernardim, Barbara; Burtoloso, Antonio Carlos Bender
Source: Tetrahedron. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERNARDIM, Barbara e BURTOLOSO, Antonio Carlos Bender. A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal. Tetrahedron, v. 70, p. 3291-3296, 2014Tradução . . Disponível em: https://doi.org/10.1016/j.tet.2013.10.059. Acesso em: 09 out. 2025.
APA
Bernardim, B., & Burtoloso, A. C. B. (2014). A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal. Tetrahedron, 70, 3291-3296. doi:10.1016/j.tet.2013.10.059
NLM
Bernardim B, Burtoloso ACB. A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal [Internet]. Tetrahedron. 2014 ; 70 3291-3296.[citado 2025 out. 09 ] Available from: https://doi.org/10.1016/j.tet.2013.10.059
Vancouver
Bernardim B, Burtoloso ACB. A two-step synthesis of the bioprotective agent JP4-039 from N-Boc- L-leucinal [Internet]. Tetrahedron. 2014 ; 70 3291-3296.[citado 2025 out. 09 ] Available from: https://doi.org/10.1016/j.tet.2013.10.059
Trabalho de evento-resumo
Diazocetonas α,β-insaturadas como precursoras de alcaloides piperidínicos e quinolizidínicos hidroxilados (2013)
Lordello, Leonardo D; Bernardim, Barbara; Burtoloso, Antonio Carlos Bender
Source: Programa e Resumos. Conference titles: Reunião Anual da Sociedade Brasileira de Química - SBQ. Unidade: IQSC
Assunto: ALCALOIDES
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ABNT
LORDELLO, Leonardo D e BERNARDIM, Barbara e BURTOLOSO, Antonio Carlos Bender. Diazocetonas α,β-insaturadas como precursoras de alcaloides piperidínicos e quinolizidínicos hidroxilados. 2013, Anais.. São Paulo: Sociedade Brasileira de Química - SBQ, 2013. Disponível em: http://www.eventoexpress.com.br/cd-36rasbq/resumos/T0534-1.pdf. Acesso em: 09 out. 2025.
APA
Lordello, L. D., Bernardim, B., & Burtoloso, A. C. B. (2013). Diazocetonas α,β-insaturadas como precursoras de alcaloides piperidínicos e quinolizidínicos hidroxilados. In Programa e Resumos. São Paulo: Sociedade Brasileira de Química - SBQ. Recuperado de http://www.eventoexpress.com.br/cd-36rasbq/resumos/T0534-1.pdf
NLM
Lordello LD, Bernardim B, Burtoloso ACB. Diazocetonas α,β-insaturadas como precursoras de alcaloides piperidínicos e quinolizidínicos hidroxilados [Internet]. Programa e Resumos. 2013 ;[citado 2025 out. 09 ] Available from: http://www.eventoexpress.com.br/cd-36rasbq/resumos/T0534-1.pdf
Vancouver
Lordello LD, Bernardim B, Burtoloso ACB. Diazocetonas α,β-insaturadas como precursoras de alcaloides piperidínicos e quinolizidínicos hidroxilados [Internet]. Programa e Resumos. 2013 ;[citado 2025 out. 09 ] Available from: http://www.eventoexpress.com.br/cd-36rasbq/resumos/T0534-1.pdf
Artigo de periodico
Alpha, beta-unsaturated diazoketones as versatile building blocks for the synthesis of hydroxylated piperidines, indolizidines and quinolizidines (2013)
Bernardim, Barbara; Lordello, Leonardo D; Burtoloso, Antonio Carlos Bender
Source: Current Topics in Medicinal Chemistry. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERNARDIM, Barbara e LORDELLO, Leonardo D e BURTOLOSO, Antonio Carlos Bender. Alpha, beta-unsaturated diazoketones as versatile building blocks for the synthesis of hydroxylated piperidines, indolizidines and quinolizidines. Current Topics in Medicinal Chemistry, v. 13, n. 17, p. 2099-2103, 2013Tradução . . Disponível em: https://repositorio.usp.br/directbitstream/d9c604a4-0d21-4ec7-ad1a-9fbe1606a01b/P14671.pdf. Acesso em: 09 out. 2025.
APA
Bernardim, B., Lordello, L. D., & Burtoloso, A. C. B. (2013). Alpha, beta-unsaturated diazoketones as versatile building blocks for the synthesis of hydroxylated piperidines, indolizidines and quinolizidines. Current Topics in Medicinal Chemistry, 13( 17), 2099-2103. Recuperado de https://repositorio.usp.br/directbitstream/d9c604a4-0d21-4ec7-ad1a-9fbe1606a01b/P14671.pdf
NLM
Bernardim B, Lordello LD, Burtoloso ACB. Alpha, beta-unsaturated diazoketones as versatile building blocks for the synthesis of hydroxylated piperidines, indolizidines and quinolizidines [Internet]. Current Topics in Medicinal Chemistry. 2013 ; 13( 17): 2099-2103.[citado 2025 out. 09 ] Available from: https://repositorio.usp.br/directbitstream/d9c604a4-0d21-4ec7-ad1a-9fbe1606a01b/P14671.pdf
Vancouver
Bernardim B, Lordello LD, Burtoloso ACB. Alpha, beta-unsaturated diazoketones as versatile building blocks for the synthesis of hydroxylated piperidines, indolizidines and quinolizidines [Internet]. Current Topics in Medicinal Chemistry. 2013 ; 13( 17): 2099-2103.[citado 2025 out. 09 ] Available from: https://repositorio.usp.br/directbitstream/d9c604a4-0d21-4ec7-ad1a-9fbe1606a01b/P14671.pdf
Trabalho de evento-resumo
Estudos visando a síntese de alcaloides indolizidínicos poliidroxilados a partir de diazocetonas α,β-insaturadas (2012)
Bernardim, Barbara; Burtoloso, Antonio Carlos Bender
Source: Programas e resumos. Conference titles: Reunião Anual da Sociedade Brasileira de Química - SBQ. Unidade: IQSC
Assunto: SÍNTESE QUÍMICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERNARDIM, Barbara e BURTOLOSO, Antonio Carlos Bender. Estudos visando a síntese de alcaloides indolizidínicos poliidroxilados a partir de diazocetonas α,β-insaturadas. 2012, Anais.. São Paulo: Sociedade Brasileira de Química, 2012. Disponível em: http://adaltech.com.br/testes/sbq/resumos/T1816-1.pdf. Acesso em: 09 out. 2025.
APA
Bernardim, B., & Burtoloso, A. C. B. (2012). Estudos visando a síntese de alcaloides indolizidínicos poliidroxilados a partir de diazocetonas α,β-insaturadas. In Programas e resumos. São Paulo: Sociedade Brasileira de Química. Recuperado de http://adaltech.com.br/testes/sbq/resumos/T1816-1.pdf
NLM
Bernardim B, Burtoloso ACB. Estudos visando a síntese de alcaloides indolizidínicos poliidroxilados a partir de diazocetonas α,β-insaturadas [Internet]. Programas e resumos. 2012 ;[citado 2025 out. 09 ] Available from: http://adaltech.com.br/testes/sbq/resumos/T1816-1.pdf
Vancouver
Bernardim B, Burtoloso ACB. Estudos visando a síntese de alcaloides indolizidínicos poliidroxilados a partir de diazocetonas α,β-insaturadas [Internet]. Programas e resumos. 2012 ;[citado 2025 out. 09 ] Available from: http://adaltech.com.br/testes/sbq/resumos/T1816-1.pdf
Artigo de periodico
Alpha, beta-unsaturated diazoketones as platforms in the asymmetric synthesis of hydroxylated alkaloids: total synthesis of 1-Deoxy-8,8a-diepicastanospermine and 1,6-dideoxypicastanospermine and formal synthesis of plumiliotoxin 251D (2012)
Bernardim, Barbara; Pinho, Vagner D; Burtoloso, Antonio Carlos Bender
Source: Journal Organic Chemistry. Unidade: IQSC
Assunto: SÍNTESE ORGÂNICA
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
ABNT
BERNARDIM, Barbara e PINHO, Vagner D e BURTOLOSO, Antonio Carlos Bender. Alpha, beta-unsaturated diazoketones as platforms in the asymmetric synthesis of hydroxylated alkaloids: total synthesis of 1-Deoxy-8,8a-diepicastanospermine and 1,6-dideoxypicastanospermine and formal synthesis of plumiliotoxin 251D. Journal Organic Chemistry, v. 77, n. 21, p. 9926-9931, 2012Tradução . . Disponível em: https://doi.org/10.1021/jo301967w. Acesso em: 09 out. 2025.
APA
Bernardim, B., Pinho, V. D., & Burtoloso, A. C. B. (2012). Alpha, beta-unsaturated diazoketones as platforms in the asymmetric synthesis of hydroxylated alkaloids: total synthesis of 1-Deoxy-8,8a-diepicastanospermine and 1,6-dideoxypicastanospermine and formal synthesis of plumiliotoxin 251D. Journal Organic Chemistry, 77( 21), 9926-9931. doi:10.1021/jo301967w
NLM
Bernardim B, Pinho VD, Burtoloso ACB. Alpha, beta-unsaturated diazoketones as platforms in the asymmetric synthesis of hydroxylated alkaloids: total synthesis of 1-Deoxy-8,8a-diepicastanospermine and 1,6-dideoxypicastanospermine and formal synthesis of plumiliotoxin 251D [Internet]. Journal Organic Chemistry. 2012 ; 77( 21): 9926-9931.[citado 2025 out. 09 ] Available from: https://doi.org/10.1021/jo301967w
Vancouver
Bernardim B, Pinho VD, Burtoloso ACB. Alpha, beta-unsaturated diazoketones as platforms in the asymmetric synthesis of hydroxylated alkaloids: total synthesis of 1-Deoxy-8,8a-diepicastanospermine and 1,6-dideoxypicastanospermine and formal synthesis of plumiliotoxin 251D [Internet]. Journal Organic Chemistry. 2012 ; 77( 21): 9926-9931.[citado 2025 out. 09 ] Available from: https://doi.org/10.1021/jo301967w

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