CARMEN NAJERA DOMINGO-rekin lankidetzan egindako argitalpenak (10)

2008

  1. A highly efficient solvent-free asymmetric direct aldol reaction organocatalyzed by recoverable (S)-binam-L-prolinamides. ESI-MS evidence of the enamine-iminium formation

    Journal of Organic Chemistry, Vol. 73, Núm. 15, pp. 5933-5943

2007

  1. Corrigendum to "High acceleration of the direct aldol reaction cocatalysed by BINAM-prolinamides and benzoic acid in aqueous media". [Tetrahedron: Asymmetry 17 (2006) 1493] (DOI:10.1016/j.tetasy.2006.05.026)

    Tetrahedron Asymmetry

  2. Corrigendum to "Organocatalyzed direct aldol condensation using l-proline and BINAM-prolinamides: regio-, diastereo-, and enantioselective controlled synthesis of 1,2-diols". [Tetrahedron: Asymmetry 17 (2006) 1027] (DOI:10.1016/j.tetasy.2006.03.023)

    Tetrahedron Asymmetry

  3. Erratum: Highly selective direct aldol reaction organocatalyzed by (S)-BINAM-L-prolinamide and benzoic acid using α-chalcogen-substituted ketones as donors (ARKIVOC (2007) iv, (260-269))

    Arkivoc

  4. Highly selective direct aldol reaction organocatalyzed by (S)-BINAM-L-prolinamide and benzoic acid using α-chalcogen-substituted ketones as donors

    Arkivoc, Vol. 2007, Núm. 4, pp. 260-269

  5. Solvent-free asymmetric direct aldol reactions organocatalysed by recoverable (Sa)-binam-l-prolinamide

    Tetrahedron Asymmetry, Vol. 18, Núm. 19, pp. 2300-2304

  6. α-Chloroacetone as a donor in the BINAM-l-prolinamide organocatalyzed aldol reaction: application to the enantioselective synthesis of α,β-epoxy ketones

    Tetrahedron Asymmetry, Vol. 18, Núm. 11, pp. 1272-1277

2006

  1. BINAM-prolinamides as recoverable catalysts in the direct aldol condensation

    Tetrahedron Asymmetry, Vol. 17, Núm. 5, pp. 729-733

  2. High acceleration of the direct aldol reaction cocatalyzed by BINAM-prolinamides and benzoic acid in aqueous media

    Tetrahedron Asymmetry, Vol. 17, Núm. 10, pp. 1493-1497

  3. Organocatalyzed direct aldol condensation using l-proline and BINAM-prolinamides: regio-, diastereo-, and enantioselective controlled synthesis of 1,2-diols

    Tetrahedron Asymmetry, Vol. 17, Núm. 7, pp. 1027-1031