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Synfacts 2010(8): 0950-0950
DOI: 10.1055/s-0030-1257799
DOI: 10.1055/s-0030-1257799
Organo- and Biocatalysis
© Georg Thieme Verlag
Stuttgart ˙ New York
Inversion of Enantioselectivity in Proline Catalysis by Basic Additives
D. G. Blackmond*, A. Moran, M. Hughes, A. Armstrong*
Imperial College London, UK
Further Information
Publication History
Publication Date:
22 July 2010 (online)

Significance
A study towards the influence of base additives in the secondary amine catalyzed α-amination of aldehydes is presented. In these experiments DBU proved to have a crucial role on the stereochemical outcome of the transformation. Whereas the reaction without additives furnished the corresponding products with (R)-configuration and high enantioselectivity, the addition of DBU inverts the new stereocenter, albeit resulting in only moderate optical purity. A mechanistic rationale, involving interactions of the base with the carboxylate catalyst moiety, is provided.