Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives (2016)
- Authors:
- Autor USP: EMERY, FLAVIO DA SILVA - FCFRP
- Unidade: FCFRP
- DOI: 10.1021/acs.joc.6b01329
- Subjects: QUÍMICA ORGÂNICA; REAÇÕES ORGÂNICAS
- Language: Inglês
- Imprenta:
- Source:
- Título: The Journal of Organic Chemistry
- ISSN: 0022-3263
- Volume/Número/Paginação/Ano: v. 81, n. 21, p. 10339-10347, 2016
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
FUMAGALLI, Fernando e EMERY, Flavio da Silva. Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives. The Journal of Organic Chemistry, v. 81, n. 21, p. 10339-10347, 2016Tradução . . Disponível em: https://doi.org/10.1021/acs.joc.6b01329. Acesso em: 11 jan. 2026. -
APA
Fumagalli, F., & Emery, F. da S. (2016). Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives. The Journal of Organic Chemistry, 81( 21), 10339-10347. doi:10.1021/acs.joc.6b01329 -
NLM
Fumagalli F, Emery F da S. Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives [Internet]. The Journal of Organic Chemistry. 2016 ; 81( 21): 10339-10347.[citado 2026 jan. 11 ] Available from: https://doi.org/10.1021/acs.joc.6b01329 -
Vancouver
Fumagalli F, Emery F da S. Charting the chemical reactivity space of 2,3-substituted furo[2,3-b]pyridines synthesized via the heterocyclization of pyridine-N-oxide derivatives [Internet]. The Journal of Organic Chemistry. 2016 ; 81( 21): 10339-10347.[citado 2026 jan. 11 ] Available from: https://doi.org/10.1021/acs.joc.6b01329 - Pd(II)-mediated cyclodehydrogenation of formyldiarylamines-total synthesis of natural carbazoles clauraila A, clausenal and 6-methoxymurrayanine
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Informações sobre o DOI: 10.1021/acs.joc.6b01329 (Fonte: oaDOI API)
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