Synthesis of 2-aryl- and 2,5-diarylfurans and thiophenes by Suzuki–Miyaura reactions using potassium trifluoroborate salts and heteroaryltellurides (2008)
- Authors:
- Autor USP: STEFANI, HELIO ALEXANDRE - FCF
- Unidade: FCF
- DOI: 10.1071/CH08255
- Subjects: SÍNTESE ORGÂNICA; POTÁSSIO
- Language: Inglês
- Imprenta:
- Source:
- Título: Austtralian Journal of Chemistry
- ISSN: 0004-9425
- Volume/Número/Paginação/Ano: v. 61, n. 11, p. 870-873, 2008
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
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ABNT
BOTTESELLE, Giancarlo Di Vaccari et al. Synthesis of 2-aryl- and 2,5-diarylfurans and thiophenes by Suzuki–Miyaura reactions using potassium trifluoroborate salts and heteroaryltellurides. Austtralian Journal of Chemistry, v. 61, n. 11, p. 870-873, 2008Tradução . . Disponível em: https://doi.org/10.1071/CH08255. Acesso em: 17 fev. 2026. -
APA
Botteselle, G. D. V., Hough, T. L. S., Venturoso, R. C., Cella, R., Vieira, A. S., & Stefani, H. A. (2008). Synthesis of 2-aryl- and 2,5-diarylfurans and thiophenes by Suzuki–Miyaura reactions using potassium trifluoroborate salts and heteroaryltellurides. Austtralian Journal of Chemistry, 61( 11), 870-873. doi:10.1071/CH08255 -
NLM
Botteselle GDV, Hough TLS, Venturoso RC, Cella R, Vieira AS, Stefani HA. Synthesis of 2-aryl- and 2,5-diarylfurans and thiophenes by Suzuki–Miyaura reactions using potassium trifluoroborate salts and heteroaryltellurides [Internet]. Austtralian Journal of Chemistry. 2008 ; 61( 11): 870-873.[citado 2026 fev. 17 ] Available from: https://doi.org/10.1071/CH08255 -
Vancouver
Botteselle GDV, Hough TLS, Venturoso RC, Cella R, Vieira AS, Stefani HA. Synthesis of 2-aryl- and 2,5-diarylfurans and thiophenes by Suzuki–Miyaura reactions using potassium trifluoroborate salts and heteroaryltellurides [Internet]. Austtralian Journal of Chemistry. 2008 ; 61( 11): 870-873.[citado 2026 fev. 17 ] Available from: https://doi.org/10.1071/CH08255 - Synthesis of symmetrical 1,3-diynes via homocoupling reaction of n-butyl alkynyltellurides
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Informações sobre o DOI: 10.1071/CH08255 (Fonte: oaDOI API)
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