Asymmetric Michael addition of ketones to nitroolefins catalyzed by a new chiral catalyst

5Citations
Citations of this article
8Readers
Mendeley users who have this article in their library.

Abstract

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).

Cite

CITATION STYLE

APA

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

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free