Bohlmann-Rahtz cyclodehydration of aminodienones to pyridines using N-iodosuccinimide

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Abstract

Cyclodehydration of Bohlmann-Rahtz aminodienone intermediates using N-iodosuccinimide as a Lewis acid proceeds at low temperature under very mild conditions to give the corresponding 2, 3,6-trisubstituted pyridines in high yield and with total regiocontrol. © 2010 by the authors.

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Bagley, M. C., & Glover, C. (2010). Bohlmann-Rahtz cyclodehydration of aminodienones to pyridines using N-iodosuccinimide. Molecules, 15(5), 3211–3227. https://doi.org/10.3390/molecules15053211

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