Chiral phosphoramides prepared from (S)-proline were used to catalyze the allylation and crotylation of aromatic aldehydes with allylic trichlorosilanes in good enantioselective yields. Phosphoramides 44 and 4m gave chiral homoallylic alcohols and their enantiomers, respectively, with similar levels of enantioselectivity.
Mendeley helps you to discover research relevant for your work.
CITATION STYLE
Iseki, K., Kuroki, Y., Takahashi, M., Kishimoto, S., & Kobayashi, Y. (1997). Asymmetric allylation of aromatic aldehydes catalyzed by chiral phosphoramides prepared from (S)-proline. Tetrahedron, 53(10), 3513–3526. https://doi.org/10.1016/S0040-4020(97)00084-7