Abstract
We disclose herein our results concerning a study aiming at the synthesis of the highly substituted carbon skeleton of alkaloids isolated from plants of the Amaryllidaceae family. The total synthesis of the functionalized dihydroisoquinolin-5(6H)-one core, which is the bottom part of the structure of alkaloids isolated from this botanic family, is described, using Morita-Baylis-Hillman adducts as substrate. This compound should be a useful and valuable intermediate for the total synthesis of alkaloids isolated from Amaryllidaceae. ©2007 Sociedade Brasileira de Química.
Author supplied keywords
Cite
CITATION STYLE
Lopes, E. C. S., & Coelho, F. (2007). Studies toward the synthesis of Amaryllidaceae alkaloids from Morita-Baylis-Hillman adducts. A straightforward synthesis of functionalized dihydroisoquinolin-5(6H)-one core. Journal of the Brazilian Chemical Society, 18(7), 1415–1438. https://doi.org/10.1590/S0103-50532007000700019
Register to see more suggestions
Mendeley helps you to discover research relevant for your work.