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Ascorbic Acid as an Aryl Radical Inducer in the Gold-Mediated Arylation of Indoles with Aryldiazonium Chlorides
Authors:Ignacio Medina-Mercado  Eric Omar Asomoza-Solís  Dr Eduardo Martínez-González  Dr Victor Manuel Ugalde-Saldívar  Lydia Gabriela Ledesma-Olvera  Dr José Enrique Barquera-Lozada  Virginia Gómez-Vidales  Dr Joaquín Barroso-Flores  Dr Bernardo A Frontana-Uribe  Dr Susana Porcel
Institution:1. Instituto de Química, Universidad Nacional Autónoma de México, Circuito Exterior s/n, Ciudad Universitaria, Cd. Mx., 04510 México;2. Facultad de Química, Universidad Nacional Autónoma de México, Av. Universidad 3000, Coyoacán, Cd. Mx., 04510 México;3. Instituto de Química, Universidad Nacional Autónoma de México, Circuito Exterior s/n, Ciudad Universitaria, Cd. Mx., 04510 México

Centro Conjunto de Investigación en Química Sustentable, UAEM-UNAM, Carretera Toluca-Atlacomulco Km 14.5, C.P. 50200 Toluca, Estado de México, México

Abstract:In recent years interest in the development of protocols that facilitate the oxidative addition of gold to access mild cross-coupling processes mediated by this metal has increased. In this context, we report herein that ascorbic acid, a natural and readily accessible antioxidant, can be used to accelerate the oxidative addition of aryldiazonium chlorides onto AuI. The aryl–AuIII species generated in this way, has been used to prepare 3-arylindoles in a one-pot protocol starting from anilines and para-, meta-, and ortho- substituted aryldiazonium chlorides. The mechanism underlying the oxidative addition has been examined in detail based on EPR analyses, cyclic voltammetry, and DFT calculations. Interestingly, we have found that in this protocol, the chloride atom induces the AuII/AuIII oxidation step.
Keywords:antioxidants  diazo compounds  gold  indoles  oxidation
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