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dc.contributor.authorWynands, L.-
dc.contributor.authorDelacroix, S.-
dc.contributor.authorVan Nhien, A. N.-
dc.contributor.authorSoriano, Elena-
dc.contributor.authorMarco-Contelles, José-
dc.date.accessioned2014-10-22T10:22:54Z-
dc.date.available2014-10-22T10:22:54Z-
dc.date.issued2013-
dc.identifierdoi: 10.1016/j.tet.2013.04.043-
dc.identifierissn: 0040-4020-
dc.identifier.citationTetrahedron 69: 4899- 4907 (2013)-
dc.identifier.urihttp://hdl.handle.net/10261/103681-
dc.description.abstractDirect aldol reactions of acetone with aromatic aldehydes have been achieved in high yielding and enantioselective processes using glycosyl-α-aminotetrazoles as a new class of organocatalysts. Computational studies at DFT level have been performed to account for the experimental observations.-
dc.publisherElsevier-
dc.rightsclosedAccess-
dc.subjectCarbohydrate-
dc.subjecta-Aminotetrazole-
dc.subjectAldolisation-
dc.subjectDFT calculation-
dc.titleNew glycosyl-α-aminotetrazole-based catalysts for highly enantioselective aldol reactions-
dc.typeartículo-
dc.identifier.doi10.1016/j.tet.2013.04.043-
dc.date.updated2014-10-22T10:22:54Z-
dc.description.versionPeer Reviewed-
dc.language.rfc3066eng-
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