María del Carmen Hita

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

G. Guillena, C. Nájera, María del Carmen Hita, 2008, The Journal of organic chemistry.

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

G. Guillena, C. Nájera, María del Carmen Hita, 2006 .

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

G. Guillena, C. Nájera, María del Carmen Hita, 2006 .

BINAM-prolinamides as recoverable catalysts in the direct aldol condensation

G. Guillena, C. Nájera, María del Carmen Hita, 2006 .

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

G. Guillena, C. Nájera, María del Carmen Hita, 2007 .

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

G. Guillena, C. Nájera, María del Carmen Hita, 2007 .

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]

G. Guillena, C. Nájera, María del Carmen Hita, 2007 .

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

G. Guillena, C. Nájera, María del Carmen Hita, 2007 .