Synthesis of Δ1-pyrrolines via formal (3 + 2)-cycloaddition of 2H-azirines with enones promoted by visible light under continuous flow (2025)
- Authors:
- USP affiliated authors: ELLENA, JAVIER ALCIDES - IFSC ; SANTIAGO, PEDRO HENRIQUE DE OLIVEIRA - IFSC
- Unidade: IFSC
- DOI: 10.1021/acsomega.5c01416
- Subjects: DINÂMICA DOS FLUÍDOS; FOTOCATÁLISE; SOLVENTE
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Publisher place: Washington, DC
- Date published: 2025
- Source:
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
MARTELLI, Lorena Suelen Ribeiro et al. Synthesis of Δ1-pyrrolines via formal (3 + 2)-cycloaddition of 2H-azirines with enones promoted by visible light under continuous flow. ACS Omega, v. 10, n. 17, p. 18017-18028 + supporting information, 2025Tradução . . Disponível em: https://doi.org/10.1021/acsomega.5c01416. Acesso em: 28 fev. 2026. -
APA
Martelli, L. S. R., Furniel, L. G., Santiago, P. H. de O., Ellena, J., & Corrêa, A. G. (2025). Synthesis of Δ1-pyrrolines via formal (3 + 2)-cycloaddition of 2H-azirines with enones promoted by visible light under continuous flow. ACS Omega, 10( 17), 18017-18028 + supporting information. doi:10.1021/acsomega.5c01416 -
NLM
Martelli LSR, Furniel LG, Santiago PH de O, Ellena J, Corrêa AG. Synthesis of Δ1-pyrrolines via formal (3 + 2)-cycloaddition of 2H-azirines with enones promoted by visible light under continuous flow [Internet]. ACS Omega. 2025 ; 10( 17): 18017-18028 + supporting information.[citado 2026 fev. 28 ] Available from: https://doi.org/10.1021/acsomega.5c01416 -
Vancouver
Martelli LSR, Furniel LG, Santiago PH de O, Ellena J, Corrêa AG. Synthesis of Δ1-pyrrolines via formal (3 + 2)-cycloaddition of 2H-azirines with enones promoted by visible light under continuous flow [Internet]. ACS Omega. 2025 ; 10( 17): 18017-18028 + supporting information.[citado 2026 fev. 28 ] Available from: https://doi.org/10.1021/acsomega.5c01416 - Structural study of asymmetric imidazoles as coordination platforms
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Informações sobre o DOI: 10.1021/acsomega.5c01416 (Fonte: oaDOI API)
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