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Synthesis 2012; 44(24): 3743-3756
DOI: 10.1055/s-0032-1317691
DOI: 10.1055/s-0032-1317691
paper
Iron(III) Chloride Promoted Desulfitative C–C Coupling Reaction of α-Oxo Ketene Dithioacetals and Indoles: Highly Selective Synthesis of β,β-Bisindolyl and β-Indolyl α,β-Unsaturated Carbonyl Compounds
Further Information
Publication History
Received: 05 September 2012
Accepted after revision: 05 November 2012
Publication Date:
16 November 2012 (online)
Abstract
The iron(III) chloride promoted desulfitative C–C coupling of α-oxo ketene dithioacetals with indoles was developed for the synthesis of indole derivatives. In the presence of iron(III) chloride, α-oxo ketene dithioacetals reacted efficiently and highly selectively with C2-unsubstituted or C2-substituted indoles to afford excellent yields of β,β-bisindolyl or β-indolyl α,β-unsaturated carbonyl compounds, respectively.
Supporting Information
- for this article is available online at http://www.thieme-connect.com/ejournals/toc/synthesis.
- Supporting Information
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