Directing Group Assisted Nucleophilic Substitution of Propargylic Alcohols via <i>o</i>‑Quinone Methide Intermediates: Brønsted Acid Catalyzed, Highly Enantio- and Diastereoselective Synthesis of 7‑Alkynyl-12a-acetamido-Substituted Benzoxanthenes

BINOL-based, chiral phosphoric acids catalyze the substitution of 1-(o-hydroxyphenyl)­propargylic alcohols with enamides to furnish 7-alkynyl-12a-acetamido-substituted benzo­[c]­xanthenes and related heterocycles in a one-pot operation with excellent diastereo- and enantioselectivity. Ambient reaction temperature, operationally simple reaction conditions, low catalyst loading, high yields, and excellent stereocontrol are attractive features of this process and make it a highly practical and versatile transformation.