Asymmetric intramolecular oxa-Michael addition of activated α,β-unsaturated ketones catalyzed by a chiral N,N′-dioxide nickel(II) complex: Highly enantioselective synthesis of flavanones

127Citations
Citations of this article
37Readers
Mendeley users who have this article in their library.
Get full text

Abstract

(Chemical Equation Presented) The title reaction provides a promising approach for the synthesis of chiral flavanones with broad substrate scope and is tolerant to air and moisture. Good to excellent enantioselectivities and high yields were achieved for most substrates under mild conditions. © 2008 Wiley-VCH Verlag GmbH & Co. KGaA.

Cite

CITATION STYLE

APA

Wang, L., Liu, X., Dong, Z., Fu, X., & Feng, X. (2008). Asymmetric intramolecular oxa-Michael addition of activated α,β-unsaturated ketones catalyzed by a chiral N,N′-dioxide nickel(II) complex: Highly enantioselective synthesis of flavanones. Angewandte Chemie - International Edition, 47(45), 8670–8673. https://doi.org/10.1002/anie.200803326

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