Abstract
Enantioselective intramolecular conjugate addition reactions of short-lived C-O axially chiral enolates have been developed. The reactions proceeded with inversion of the configuration and provided dihydrobenzofurans with contiguous tetra- and trisubstituted carbon centers in up to 96% enantiomeric excess (ee).
Author supplied keywords
Cite
CITATION STYLE
Tomohara, K., Kasamatsu, K., Yoshimura, T., Furuta, T., & Kawabata, T. (2016). Asymmetric synthesis of multisubstituted dihydrobenzofurans by intramolecular conjugate addition of short-lived C-O axially chiral enolates. Chemical and Pharmaceutical Bulletin, 64(7), 899–906. https://doi.org/10.1248/cpb.c16-00272
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.