dc.creatorHarris, Maria Inês N. C.
dc.creatorBraga, Antonio C. H.
dc.date2004-12-01
dc.date2014-07-17T17:20:01Z
dc.date2015-11-26T11:46:56Z
dc.date2014-07-17T17:20:01Z
dc.date2015-11-26T11:46:56Z
dc.date.accessioned2018-03-28T20:50:36Z
dc.date.available2018-03-28T20:50:36Z
dc.identifierJournal of the Brazilian Chemical Society. Sociedade Brasileira de Química, v. 15, n. 6, p. 971-975, 2004.
dc.identifier0103-5053
dc.identifierS0103-50532004000600027
dc.identifier10.1590/S0103-50532004000600027
dc.identifierhttp://dx.doi.org/10.1590/S0103-50532004000600027
dc.identifierhttp://www.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532004000600027
dc.identifierhttp://www.repositorio.unicamp.br/jspui/handle/REPOSIP/25199
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/25199
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1236231
dc.descriptionReduction of beta-enamino ketones 2 with NaBH4 in glacial acetic acid gave gamma-amino alcohols 1 in 70% to 98% yield with diastereomeric excesses, preferentially the syn product, from 44% to 90%. The stereochemistry of these compounds was confirmed by analysis of their tetrahydro-1,3-oxazine derivatives 3.
dc.descriptionA redução de beta-enamino cetonas 2 com NaBH4 em ácido acético glacial produziu gama-amino álcoois 1 em 70% a 98% de rendimento, com excessos diastereoméricos, preferencialmente o produto syn, de 44% a 90%. A estereoquímica desses compostos foi confirmada pela análise de seus derivados tetraidro-1,3-oxazinas 3.
dc.description971
dc.description975
dc.languageen
dc.publisherSociedade Brasileira de Química
dc.relationJournal of the Brazilian Chemical Society
dc.rightsaberto
dc.sourceSciELO
dc.subjectamino alcohols
dc.subjectenamino ketones
dc.subjectoxazines
dc.subjectstereoselective reduction
dc.titleAn easy and efficient method to produce gamma-amino alcohols by reduction of beta-enamino ketones
dc.typeArtículos de revistas


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