Diastereoselective Synthesis of Tetrabenzohydrofuran Spirooxindoles via Diethyl Phosphite-Mediated Coupling of Isatins with -Quinone Methides.

Diethyl phosphite-initiated coupling of isatins with -quinone methides (-QMs) is reported. This reaction involves a cascade transformation initiated by base-promoted addition of phosphite to isatins, followed by [1,2]-phospha-Brook rearrangement. This generates α-phosphonyloxy enolates that are subsequently intercepted by -QMs and finally intramolecular ring closure. This protocol was used to diastereoselectively synthesize a range of -tetrabenzohydrofuran spirooxindoles in moderate to good yields with moderate to excellent diastereoselectivities.