Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones (2019)
- Authors:
- USP affiliated authors: STEFANI, HELIO ALEXANDRE - FCF ; SHAMIM, ANWAR - IQSC
- Unidades: FCF; IQSC
- DOI: 10.1002/adsc.201900564
- Subjects: ALDEÍDOS; ESTEREOQUÍMICA
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título: Advanced Synthesis & Catalysis
- ISSN: 1615-4169
- Volume/Número/Paginação/Ano: v. 361, p. 4243-4254, 2019
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
VASCONCELOS, Stanley Nunes Siqueira et al. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones. Advanced Synthesis & Catalysis, v. 361, p. 4243-4254, 2019Tradução . . Disponível em: https://doi.org/10.1002/adsc.201900564. Acesso em: 13 fev. 2026. -
APA
Vasconcelos, S. N. S., Oliveira, I. M. de, Shamim, A., Zukerman-Schpector, J., Pimenta, D. C., & Stefani, H. A. (2019). Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones. Advanced Synthesis & Catalysis, 361, 4243-4254. doi:10.1002/adsc.201900564 -
NLM
Vasconcelos SNS, Oliveira IM de, Shamim A, Zukerman-Schpector J, Pimenta DC, Stefani HA. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones [Internet]. Advanced Synthesis & Catalysis. 2019 ; 361 4243-4254.[citado 2026 fev. 13 ] Available from: https://doi.org/10.1002/adsc.201900564 -
Vancouver
Vasconcelos SNS, Oliveira IM de, Shamim A, Zukerman-Schpector J, Pimenta DC, Stefani HA. Stereoselective oxa‐Michael addition of tyrosine to propargyl aldehyde/esters: formation of benzofurans and flavones [Internet]. Advanced Synthesis & Catalysis. 2019 ; 361 4243-4254.[citado 2026 fev. 13 ] Available from: https://doi.org/10.1002/adsc.201900564 - Antioxidant and anti-sickling activity of glucal-based triazoles compounds – an in vitro and in silico study
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Informações sobre o DOI: 10.1002/adsc.201900564 (Fonte: oaDOI API)
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