A new chiral catalyst was synthesized and found that it could catalyzed the asymmetric Michael reaction of ketones with nitroolefins smoothly at room temperature, giving the desired adducts in 71 - 92% yields with excellent diastereoselectivities and high enantioselectivities (up to 95% ee).
CITATION STYLE
Wang, L. J., & Hu, F. F. (2010). Asymmetric Michael addition of ketones to nitroolefins catalyzed by a new chiral catalyst. Bulletin of the Korean Chemical Society, 31(5), 1280–1282. https://doi.org/10.5012/bkcs.2010.31.5.1280
Mendeley helps you to discover research relevant for your work.