Mostrar registro simples

Diastereosseletividade na redução de enonas bicíclicas com hidretos volumosos

dc.contributor.authorCamozzato, Andreza Casanovapt_BR
dc.contributor.authorTenius, Beatriz Soares Machadopt_BR
dc.contributor.authorOliveira, Eduardo Rolim dept_BR
dc.contributor.authorViegas Junior, Claudiopt_BR
dc.contributor.authorVictor, Mauricio Moraespt_BR
dc.contributor.authorSilveira, Leandro Greff dapt_BR
dc.date.accessioned2013-07-02T01:43:16Zpt_BR
dc.date.issued2008pt_BR
dc.identifier.issn0100-4042pt_BR
dc.identifier.urihttp://hdl.handle.net/10183/72873pt_BR
dc.description.abstractReduction of five substituted octalones employing lithium tri-sec-butylborohydride (L-selectride®) in THF and ethyl ether led to allylic alcohols with moderate diastereoselectivity. The stereoselectivity of addition of bulky hydrides showed to be different from most examples in the literature and was strongly influenced by substitution on the octalone ring.en
dc.format.mimetypeapplication/pdfpt_BR
dc.language.isoporpt_BR
dc.relation.ispartofQuímica nova. São Paulo. Vol. 31, n. 4 (jun. 2008), p. 793-797pt_BR
dc.rightsOpen Accessen
dc.subjectOctalonesen
dc.subjectEnquadramento sindical : Brasilpt_BR
dc.subjectEnonas : Redução diastereosseletivapt_BR
dc.subjectReductionen
dc.subjectL-selectride®en
dc.subjectSíntese orgânicapt_BR
dc.titleDiastereosseletividade na redução de enonas bicíclicas com hidretos volumosospt_BR
dc.title.alternativeDiastereoselectivity in the reduction of bicyclic enones with hindered hydrides en
dc.typeArtigo de periódicopt_BR
dc.identifier.nrb000682593pt_BR
dc.type.originNacionalpt_BR


Thumbnail
Nome:
000682593.pdf
Tamanho:
289.7Kb
Formato:
PDF
Descrição:
Texto completo
Visualizar/abrir
   

Este item está licenciado na Creative Commons License

Mostrar registro simples