An enantioselective synthesis of isoquinuclidines from 3-substituted chiral pyridinium salts.

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dc.contributor.authorSantos, Daniela Cristina dos
dc.contributor.authorGil, Rossimiriam Pereira de Freitas
dc.contributor.authorGil, Laurent Frédéric
dc.contributor.authorMarazano, Christian
dc.date.accessioned2015-04-17T15:31:53Z
dc.date.available2015-04-17T15:31:53Z
dc.date.issued2001
dc.description.abstractA new enantioselective approach to chiral isoquinuclidines, such as 15, 18 and 21, is reported. The key step of these syntheses is a cycloaddition between chiral dihydropyridines 14 or 20, now readily available from tetrahydropyridinium salts 6 or 11, and achiral dienophiles. The reaction proceeds with a very good endo-selectivity and moderate d.e.pt_BR
dc.identifier.citationSANTOS, D. C. dos et al. An enantioselective synthesis of isoquinuclidines from 3-substituted chiral pyridinium salts. Tetrahedron Letters, v. 42, p. 6109-6111, 2001. Disponível em: <http://www.sciencedirect.com/science/article/pii/S0040403901011947>. Acesso em: 02 fev. 2015.pt_BR
dc.identifier.doihttps://doi.org/10.1016/S0040-4039(01)01194-7
dc.identifier.issn0040-4039
dc.identifier.urihttp://www.repositorio.ufop.br/handle/123456789/5124
dc.language.isoen_USpt_BR
dc.rights.licenseO periódico Tetrahedron Letters concede permissão para depósito deste artigo no Repositório Institucional da UFOP. Número da licença: 3581981445773.pt_BR
dc.titleAn enantioselective synthesis of isoquinuclidines from 3-substituted chiral pyridinium salts.pt_BR
dc.typeArtigo publicado em periodicopt_BR
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