Activation of 1, 2??Keto Esters with Takemoto's Catalyst toward Michael Addition to Nitroalkenes

…, T Constantieux, D Bonne, J Rodriguez

Index: Raimondi, Wilfried; Basle, Olivier; Constantieux, Thierry; Bonne, Damien; Rodriguez, Jean Advanced Synthesis and Catalysis, 2012 , vol. 354, # 4 p. 563 - 568

Full Text: HTML

Citation Number: 20

Abstract

In continuation to our ongoing studies on conjugate additions to nitroolefins,8 we became interested in the challenging reactivity of α-keto esters as pronucleophiles in organocatalyzed Michael reactions since no example of such a transformation has been reported so far.9,10 Our own interest in the activation of 1,2-dicarbonyl compounds11 and the very recent report from Terada and co-workers on an unprecedented enantioselective organocatalyzed amination of α-keto ...

Related Articles:

Oxidation of. alpha.-ketoacyl derivatives. Rearrangement of pyruvates to malonates

[Rueppel,M.L.; Rapoport,H. Journal of the American Chemical Society, 1972 , vol. 94, p. 3877 - 3883]

More Articles...