Synfacts 2008(7): 0731-0731  
DOI: 10.1055/s-2008-1078465
Metal-Catalyzed Asymmetric Synthesis and Stereoselective Reactions
© Georg Thieme Verlag Stuttgart · New York

Enantioselective Synthesis of Quaternary l-Valine Derivatives

Contributor(s): Mark Lautens, Praew Thansandote
M. Branca, D. Gori, R. Guillot, V. Alezra*, C. Kouklovsky*
Université Paris-Sud, France
Weitere Informationen

Publikationsverlauf

Publikationsdatum:
20. Juni 2008 (online)

Significance

The authors present an enantioselective synthesis of l-valine derivatives using the memory of chirality from tertiary aromatic amides incorporated onto l-valine. Alkylation of these derivatives is performed by using a strong base (KHMDS) and reactive electrophiles (such as triflates), though less reactive electrophiles can be used with DMPU as an additive. Reaction times are short to decrease racemization of the enolate and increase ee values. The ee values can be improved by recrystallization for all compounds.