Expanding the chemical diversity of spirooxindoles via alkylative pyridine dearomatization

Abstract

A mild and practical synthesis of spirooxindole [1,3]oxazino derivatives from N-substituted isatins and 1,3-dicarbonyl compounds with pyridine derivatives is reported. The reactions provided good to excellent yields. Further exploration of the molecular diversity of these compounds is demonstrated through Diels–Alder reactions.

Keywords

• chemical diversity
• 1,3-dicarbonyl compounds
• Diels–Alder reaction
• molecular diversity
• pyridine dearomatization
• spirooxindole