A Highly Efficient Solvent-Free Asymmetric Direct Aldol Reaction Organocatalyzed by Recoverable (S)-Binam-l-Prolinamides. ESI-MS Evidence of the Enamine−Iminium Formation
Guillena, Gabriela, Hita, Maria del Carmen, Nájera, Carmen, Viózquez, Santiago F
Published in Journal of organic chemistry (01.08.2008)
Published in Journal of organic chemistry (01.08.2008)
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BINAM-prolinamides as recoverable catalysts in the direct aldol condensation
Guillena, Gabriela, del Carmen Hita, María, Nájera, Carmen
Published in Tetrahedron: asymmetry (06.03.2006)
Published in Tetrahedron: asymmetry (06.03.2006)
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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]
Guillena, Gabriela, del Carmen Hita, María, Nájera, Carmen
Published in Tetrahedron: asymmetry (16.05.2007)
Published in Tetrahedron: asymmetry (16.05.2007)
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Corrigendum to “High acceleration of the direct aldol reaction cocatalysed by BINAM-prolinamides and benzoic acid in aqueous media”: [Tetrahedron: Asymmetry 17 (2006) 1493]
Guillena, Gabriela, del Carmen Hita, María, Nájera, Carmen
Published in Tetrahedron: asymmetry (16.05.2007)
Published in Tetrahedron: asymmetry (16.05.2007)
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ChemInform Abstract: A Highly Efficient Solvent-Free Asymmetric Direct Aldol Reaction Organocatalyzed by Recoverable (S)-Binam-L-prolinamides. ESI-MS Evidence of the Enamine-Iminium Formation
Guillena, Gabriela, Hita, Maria del Carmen, Najera, Carmen, Viozguez, Santiago F.
Published in ChemInform (23.12.2008)
Published in ChemInform (23.12.2008)
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