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One‐Pot Synthesis of O‐Allylhydroxylamines through the Organocatalytic Oxidation of Tertiary Allylic Amines Followed by a [2,3]‐Meisenheimer Rearrangement
Authors:Alexis Theodorou  Dr. Dimitris Limnios  Prof. Dr. Christoforos G. Kokotos
Affiliation:Laboratory of Organic of Chemistry, Department of Chemistry, University of Athens, Panepistimiopolis 15771, Athens (Greece)
Abstract:A cheap, green, and highly efficient one‐pot method for the synthesis of O‐protected allylic alcohols is described. By utilizing 2,2,2‐trifluoroacetophenone as the organocatalyst and H2O2 as the oxidant, a variety of allylic amine N‐oxides were synthesized, which upon heating are converted to the final products through a [2,3]‐Meisenheimer rearrangement.
Keywords:alcohols  green chemistry  organocatalysis  oxidation  rearrangement
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