3543-42-8Relevant articles and documents
Highly enantioselective synthesis of optically active ketones by iridium-catalyzed asymmetric hydrogenation
Lu, Sheng-Mei,Bolm, Carsten
supporting information; experimental part, p. 8920 - 8923 (2009/05/30)
(Chemical Equation Presented) Close to perfect enantioselectivity (up to 99% ee, see scheme) is found for the formation of α-substituted ketones by the asymmetric hydrogenation of enones with an iridium-phosphinooxazoline catalyst. In an operationally simple process, both linear and cyclic substrates react well and afford the desired products in high yields. A wide variety of substituents are tolerated, thus making the method synthetically appealing.
Double Michael addition reactions of some new 1,5-diaryl-2-alkyl-1,4-pentadien-3-ones: Part II
Padmavathi,Ramana Reddy,Venugopal Reddy,Audisesha Reddy,Bhaskar Reddy
, p. 667 - 673 (2007/10/03)
The reactivity of unsymmetrical 1,5-diaryl-2-alkyl-l,4-pentadien-3-ones with active methylene compounds has been studied. The structures of the compounds have been established by spectral parameters.