Metal-Free Brønsted Acid-Catalyzed Rearrangement of δ‑Hydroxyalkynones to 2,3-Dihydro‑4<i>H</i>‑pyran-4-ones: Total Synthesis of Obolactone and a Catechol Pyran Isolated from <i>Plectranthus sylvestris</i>

A metal-free, Brønsted acid, pTsOH-catalyzed intramolecular rearrangement of δ-hydroxyalkynones to substituted 2,3-dihydro-4H-pyran-4-ones was developed. The rearrangement occurs with high regioselectivity under mild and open-air conditions. The scope of work was illustrated by synthesizing an array of aliphatic and aromatic substituted 2,3-dihydro-4H-pyran-4-ones in up to 96% yield, 100% atom economy, and complete regioselectivity. Some of the dihydropyranones are utilized for vinylic halogenations and to complete the total synthesis of bioactive natural products, obolactone and a catechol pyran isolated from Plectranthus sylvestris (Labiatae).