bohlmann-rahtz cyclodehydration of aminodienones to pyridines using n-iodosuccinimide
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bohlmann-rahtz cyclodehydration of aminodienones to pyridines using n-iodosuccinimide

;Mark C. Bagley;Christian Glover
Journal of ethnopharmacology 2010 Vol. 15 pp. 3211-3227
155
bagley2010moleculesbohlmann-rahtz

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.

Keywords

heterocycles pyridinesorganic chemistry

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DOI:
10.3390/molecules15053211
URL:
http://www.mdpi.com/1420-3049/15/5/3211/

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ID: 248559
Ref Key: bagley2010moleculesbohlmann-rahtz
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