Synthesis of indolines via a SmI promoted domino nitro reduction-intramolecular aza-Michael reaction.

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Autor(es): dc.creatorRamos, Josierika Alexandra Ferreira-
Autor(es): dc.creatorAraujo, Carolina Soares-
Autor(es): dc.creatorNagem, Tanus Jorge-
Autor(es): dc.creatorTaylor, Jason Guy-
Data de aceite: dc.date.accessioned2025-08-21T15:42:20Z-
Data de disponibilização: dc.date.available2025-08-21T15:42:20Z-
Data de envio: dc.date.issued2017-06-20-
Data de envio: dc.date.issued2017-06-20-
Data de envio: dc.date.issued2015-
Fonte completa do material: dc.identifierhttp://www.repositorio.ufop.br/handle/123456789/8005-
Fonte completa do material: dc.identifierhttp://onlinelibrary.wiley.com/doi/10.1002/jhet.1982/abstract-
Fonte completa do material: dc.identifierhttps://doi.org/10.1002/jhet.1982-
Fonte: dc.identifier.urihttp://educapes.capes.gov.br/handle/capes/1022065-
Descrição: dc.descriptionA simple and straightforward synthesis of substituted indolines based on a domino nitro reduction intramolec-ular aza-Michael reaction is described. The reaction employs Samarium diiodide under mild conditions for theaddition of dibromoacetic acid to substituted 2-(2-nitrophenyl) acetaldehyde derivatives and their subsequent cycli-zation upon nitro group reduction to provide corresponding indoline heterocycles in good yields. This “one pot”strategy also permitted the expeditious synthesis of a 1,2,3,4-tetrahydroquinoline, whereas the seven-membered2,3,4,5-tetrahydrobenzoazepines compounds were not formed under these reaction conditions.-
Formato: dc.formatapplication/pdf-
Idioma: dc.languageen-
Direitos: dc.rightsrestrito-
Título: dc.titleSynthesis of indolines via a SmI promoted domino nitro reduction-intramolecular aza-Michael reaction.-
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