A benzyne route to indoles from o- or m-bromoaryl ketones
- 1 January 1979
- journal article
- research article
- Published by Royal Society of Chemistry (RSC) in Journal of the Chemical Society, Perkin Transactions 1
- p. 827-828
- https://doi.org/10.1039/p19790000827
Abstract
Indoles (11) or (14) are formed directly when 2-amino-1-o-(or m-)bromoaryl-ethanols (8) or (13) are treated with potassamide in liquid ammonia.Keywords
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