Diastereoselective Synthesis of Chromeno[3,2‑d]isoxazoles via Brønsted Acid Catalyzed Tandem 1,6-Addition/Double Annulations of o‑Hydroxyl Propargylic Alcohols

A Brønsted acid catalyzed tandem process to access densely functionalized chromeno­[3,2-d]­isoxazoles with good to excellent yields and diastereoselectivities was disclosed. The procedure is proposed to involve a 1,6-conjugate addition/electrophilic addition/double annulations process of alkynyl o-quinone methides (o-AQMs) in situ generated from o-hydroxyl propargylic alcohols with nitrones. Mild conditions, good functional group compatibility, easy scale-up of the reaction, and further product transformation demonstrated its potential application.