Synlett 2017; 28(02): 260-264
DOI: 10.1055/s-0036-1588335
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© Georg Thieme Verlag Stuttgart · New York

Lewis Acid Mediated Addition of Indoles and Alcohols to Tetronic Acid and Tetramic Acids

Fernando Banales Mejia
Department of Chemistry, Hobart and William Smith Colleges, Geneva, NY, 14456, USA   Email: pelkey@hws.edu
,
Megan M. Lafferty
Department of Chemistry, Hobart and William Smith Colleges, Geneva, NY, 14456, USA   Email: pelkey@hws.edu
,
Sophia J. Melvin
Department of Chemistry, Hobart and William Smith Colleges, Geneva, NY, 14456, USA   Email: pelkey@hws.edu
,
Nathanyal J. Truax
Department of Chemistry, Hobart and William Smith Colleges, Geneva, NY, 14456, USA   Email: pelkey@hws.edu
,
Maeve H. Kean
Department of Chemistry, Hobart and William Smith Colleges, Geneva, NY, 14456, USA   Email: pelkey@hws.edu
,
Erin T. Pelkey*
Department of Chemistry, Hobart and William Smith Colleges, Geneva, NY, 14456, USA   Email: pelkey@hws.edu
› Author Affiliations
Further Information

Publication History

Received: 09 August 2016

Accepted after revision: 22 September 2016

Publication Date:
13 October 2016 (online)


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Abstract

The electrophilic substitution of indoles with tetronic acid and N-acetyltetramic acid mediated by BF3·OEt2 was investigated. This strategy allowed for the preparation of nine indole-substituted furan-2-ones (indolyl-γ-lactones) and 3-pyrrolin-2-ones (indolyl-γ-lactams) and is more straightforward than previously reported synthetic methods. During the course of our investigation, we also discovered a facile synthesis of tetronates and a tetramate via a BF3-mediated addition of alcohols to tetronic acid and N-acetyltetramic acid, respectively.

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