Abstract
Abstract The intermolecular Knoevenagel condensation of β-hemiacetyl ester proceeds by an in situ unmasking of a reactive ω-hydroxy-β-keto ester giving unsaturated ω-hydroxy-β-keto esters 6–12 which accommodate acetal formation.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have