Calcium‐Catalyzed Synthesis of Polysubstituted 2‐Alkenylfurans from β‐Keto Esters Tethered to Propargyl Alcohols

as a catalytic mixture is described. It is based on the cycloelimination of readily available propargyl alcohols tethered to β-keto esters under dry conditions to avoid competitive Meyer-Schuster rearrangement. The furan can be further functionalized in situ by a calcium-catalyzed Friedel-Crafts-type reaction with secondary and tertiary alcohols. The title reaction allows for the high-yielding preparation of di-, tri-, and tetrasubstituted 2-alkenylfurans, which are important subunits of bioactive compounds.