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Synthesis 2018; 50(24): 4829-4836
DOI: 10.1055/s-0037-1610181
DOI: 10.1055/s-0037-1610181
paper
Divergent Reactivity of Indole-Tethered Ynones with Silver(I) and Gold(I) Catalysts: A Combined Synthetic and Computational Study
This work was conducted using funding from EPSRC (EP/M018601/01, J.T.R.L. and EP/R013748/1, A.K.C.), the University of York (J.A.R.-A., A.K.C., W.P.U.) and the Leverhulme Trust (Early Career Fellowship, ECF-2015-13, W.P.U.).
Further Information
Publication History
Received: 27 March 2018
Accepted after revision: 16 May 2018
Publication Date:
04 July 2018 (online)
Abstract
A combined synthetic and computational (DFT) study has been performed to account for the divergent reactivity of indole-tethered ynones when treated with Ag(I) and Au(I) catalysts. The two catalyst systems deliver spirocyclic indolenines and carbazoles, respectively, from the same precursors, with the reaction outcomes believed to be a result of differences in the rates of a key protodemetalation step. A ring-opening/ring-closing isomerisation process is proposed to enable the interconversion of spirocyclic and C-2 annulated indole intermediates, in contrast to the 1,2-migration mechanism tentatively proposed in previous studies.
Supporting Information
- Supporting information for this article is available online at https://doi.org/10.1055/s-0037-1610181. Included are details of the computational methods, energies, xyz coordinates and vibrational modes for calculated structures.
- Supporting Information
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For recent catalyst selective synthesis methods, see:
For examples from our groups, see:
For related papers on the cyclisation of electron-rich aromatics onto tethered alkynes from our groups, see:
For important contributions from other groups, see:
For related methods to prepare carbazoles, see:
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For reviews on gold catalysis, see:
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