Abstract
By modifying the conditions from those in Larock's reported synthesis of 3-(2-hydroxyaryl)pyridines from benzynes, and pyridine N-oxides, we altered the regioselectivity of the reaction toward an efficient synthesis of 2-substituted pyridines. The presence of ethyl propiolate altered the regioselectivity to afford 3-substituted pyridine products instead. We conducted appropriate control experiments that enable a full understanding of the mechanism. © 2012 The Royal Society of Chemistry.
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CITATION STYLE
Shaibu, B. S., Kawade, R. K., & Liu, R. S. (2012). Regioselective synthesis of 2-(2-hydroxyaryl)pyridines from the reactions of benzynes with pyridine N-oxides. Organic and Biomolecular Chemistry, 10(34), 6834–6839. https://doi.org/10.1039/c2ob26130h
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