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Tunable Electrocatalytic Annulations of <i>o-</i>Arylalkynylanilines: Green and Switchable Syntheses of Skeletally Diverse Indoles

Jie Zhang, Shaoqing Shi, Wen‐Juan Hao, Guo-Yun Dong, Shu‐Jiang Tu, Bo Jiang

2021The Journal of Organic Chemistry29 citationsDOI

Abstract

Tunable electrocatalytic annulation reactions of o-arylalkynylanilines have been established, leading to green and divergent syntheses of skeletally diverse indoles by adjusting the electrolytes and the solvents. The presence of ammonium halides as the electrolytes enabled the halogenation of o-arylalkynylanilines to give C3-halogenated indoles whereas naphtho[1′,2′:4,5]furo[3,2-b]indoles could be obtained by changing the electrolyte from ammonium halides to KI. Interestingly, by combining acetone as the solvent and both NH4I and NH4Cl as the electrolytes, the reaction worked through an intramolecular annulation and [5 + 1] cyclization cascade to form naphtho[1′,2′:5,6][1,3]oxazino[3,4-a]indoles.

Topics & Concepts

ChemistryCombinatorial chemistryRadical Photochemical ReactionsCatalytic C–H Functionalization MethodsSulfur-Based Synthesis Techniques
Tunable Electrocatalytic Annulations of <i>o-</i>Arylalkynylanilines: Green and Switchable Syntheses of Skeletally Diverse Indoles | Litcius