Electrosynthesis of Dihydropyrano[4, 3‐b]indoles Based on a Double Oxidative [3+3] Cycloaddition. (18th May 2020)

• Record Type: Journal Article
• Authors: Choi, Subin; Park, Jinhwi; Yu, Eunsoo; Sim, Jeongwoo; Park, Cheol‐Min
• Is Part Of: Angewandte Chemie. Volume 132:Number 29(2020)
• Page Start: 11984
• Page End: 11989
• Publication Date: 2020-05-18
• Subjects: [3+3] cycloaddition -- electrochemistry -- hydrogen atom transfer -- indoles -- radical chemistry; Chemistry -- Periodicals; 540
• DOI: 10.1002/ange.202003364
• Languages: English
• ISSNs: 0044-8249

Abstract

Abstract: Oxidative [3+3] cycloadditions offer an efficient route for six‐membered‐ring formation. This approach has been realized based on an electrochemical oxidative coupling of indoles/enamines with active methylene compounds followed by tandem 6π‐electrocyclization leading to the synthesis of dihydropyrano[4, 3‐ b ]indoles and 2, 3‐dihydrofurans. The radical–radical cross‐coupling of the radical species generated by anodic oxidation combined with the cathodic generation of the base from O2 allows for mild reaction conditions for the synthesis of structurally complex heterocycles. Abstract : Oxidative [3+3] cycloadditions constitute an efficient approach for the generation of six‐membered rings. Such a strategy was realized through an electrochemical oxidative coupling of indoles/enamines with active methylene compounds followed by tandem cyclization to generate dihydropyrano[4, 3‐ b ]indoles and 2, 3‐dihydrofurans.