Approach to the enantioselective synthesis of achillifoline

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Antonio Rosales
Juan Muñoz Bascón
José Antonio Castilla Alcalá
Esther Roldán Molina
Santiago Olmedo
Janeth Proaño
J Enrique Oltra

Abstract

In this paper, an approximation biomimetic synthesis of achillifoline, a natural sesquiterpene lactone isolated from Achillea millefolium subsp. Millenium, is presented. Carbocationic cyclization of epoxy-costunolide is the key step of the synthetic sequence. This transannular cyclization, allows the formation of the skeleton of 1,4-epoxy-cyclodecane presents in achillifoline

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How to Cite
1.
Rosales A, Muñoz Bascón J, Castilla Alcalá JA, Roldán Molina E, Olmedo S, Proaño J, Oltra JE. Approach to the enantioselective synthesis of achillifoline. REMCB [Internet]. 2017Aug.15 [cited 2024Jul.3];35(1-2):41-0. Available from: https://remcb-puce.edu.ec/remcb/article/view/257
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Artículos Científicos