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Bohlmann-Rahtz Cyclodehydration of Aminodienones to Pyridines Using N-iodosuccinimide

Overview
Journal Molecules
Publisher MDPI
Specialty Biology
Date 2010 Jul 27
PMID 20657473
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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.

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