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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Revisiting the Intermolecular Fujiwara Hydroarylation of Alkynes

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Author(s):
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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.
Total Authors: 11
Document type: Journal article
Source: EUROPEAN JOURNAL OF ORGANIC CHEMISTRY; v. 2017, n. 13, p. 1794-1803, APR 3 2017.
Web of Science Citations: 9
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. (AU)

FAPESP's process: 10/00257-3 - Mechanistic Studies of Catalytic Direct Arylation Reactions of Heteroaromatics using Mass Spectrometry.
Grantee:Marla Narciso Godoi
Support type: Scholarships in Brazil - Post-Doctorate
FAPESP's process: 08/00122-0 - Synthetic Applications of the Petasis Reactions of N-acyliminium Ions. Use of enecarbamates in organocatalysis and in the synthesis of sphingosines analogues.
Grantee:Pablo David Grigol Martinez
Support type: Scholarships in Brazil - Doctorate
FAPESP's process: 10/11068-7 - C-H activations catalysed by Pd(II) and Rh(III): methodological and mechanistic studies to the synthesis of diarylethane and congeners and evaluations of its biological activity
Grantee:Francisco de Azambuja
Support type: Scholarships in Brazil - Doctorate
FAPESP's process: 11/23832-6 - New methodological and mechanistic studies related to the Heck arylations employing arenediazonium salts and synthetic applications
Grantee:Carlos Roque Duarte Correia
Support type: Regular Research Grants