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Issue 7, 2006
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Organocatalytic C3-selective Friedel–Crafts alkylations of indoles with α,β-unsaturated ketones

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Abstract

The use of an equimolar amount of pyrrolidine and HClO4 (30 mol%) was found to be effective in promoting the conjugate addition of indoles to (E)-α,β-unsaturated ketones, affording the corresponding β-indolyl ketones in excellent yields.

Graphical abstract: Organocatalytic C3-selective Friedel–Crafts alkylations of indoles with α,β-unsaturated ketones

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Publication details

The article was received on 17 Oct 2005, accepted on 10 Jan 2006 and first published on 19 Jan 2006


Article type: Communication
DOI: 10.1039/B514648H
Citation: Chem. Commun., 2006, 799-801
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    Organocatalytic C3-selective Friedel–Crafts alkylations of indoles with α,β-unsaturated ketones

    D. Li, Y. Guo, Y. Ding and W. Xiao, Chem. Commun., 2006, 799
    DOI: 10.1039/B514648H

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