Please use this identifier to cite or link to this item: http://repositorio.unicamp.br/jspui/handle/REPOSIP/328419
Type: Artigo
Title: Revisiting The Intermolecular Fujiwara Hydroarylation Of Alkynes
Author: Godoi
Marla N.; de Azambuja
Francisco; Martinez
Pablo David G.; Morgon
Nelson H.; Santos
Vanessa G.; Regiani
Thais; Lesage
Denis; Dossmann
Heloise; Cole
Richard B.; Eberlin
Marcos N.; Correia
Carlos Roque D.
Abstract: The Fujiwara hydroarylation of alkynes was reinvestigated using the addition of indole to methyl or ethyl phenyl-propiolate catalyzed by Pd(OAc)(2) as a model reaction. Reactions were monitored by both H-1 NMR spectroscopy and electrospray ionization mass spectrometry (ESI/MS), and also through reactions carried out in the gas phase using MS/MS experiments. Contrary to the original suggestion for exclusive heteroarene activation, the data supports the coexistence of both heteroarene activation (C-H activation) and alkyne activation (Friedel-Crafts- type pathway). Under the reaction conditions used in this work, intermediates for both mechanisms were detected by NMR spectroscopy and MS, but alkyne activation seems to be predominant according to H-1 NMR spectroscopic studies and theoretical predictions. Alkyne activation is promoted by the coordination of an electrophilic palladium species to the C-C triple bond, followed by nucleophilic attack of the heteroaryl counterpart. Two previously undetected equilibria in this reaction involving the vinylpalladium intermediates and the final products were also found to be critical to the stereoselectivity of the reaction.
Subject: Fujiwara Reaction
Hydroheteroarylation
Alkynes
Indoles
Cross-coupling
Editor: Wiley-V C H Verlag GMBH
Weinhem
Citation: European Journal Of Organic Chemistry. Wiley-v C H Verlag Gmbh, p. 1794 - 1803, 2017.
Rights: fechado
Identifier DOI: 10.1002/ejoc.201700033
Address: http://onlinelibrary.wiley.com/doi/10.1002/ejoc.201700033/abstract
Date Issue: 2017
Appears in Collections:Unicamp - Artigos e Outros Documentos

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