Abstract
We report herein the concise preparation of a range of functionalised aminoindoles via a new application of the Bartoli reaction. Scope and limitations of the methodology have been extensively studied to reveal the importance of protecting groups and substitution patterns. The use of amino substituted nitroanilines for the Bartoli reaction is to our knowledge unprecedented. Our work thus represents a novel entry into substituted aminoindoles which are relevant building blocks for both the fine chemical and pharmaceutical industry. © 2012 The Royal Society of Chemistry.
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CITATION STYLE
Wylie, L., Innocenti, P., Whelligan, D. K., & Hoelder, S. (2012). Synthesis of amino-substituted indoles using the Bartoli reaction. Organic and Biomolecular Chemistry, 10(22), 4441–4447. https://doi.org/10.1039/c2ob25256b
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