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Terminal oxazolinyloxiranes: synthesis, reaction with amines and regioselective b-lithiation

Academic Article
Publication Date:
2009
abstract:
The synthesis of terminal oxazolinyloxiranes, even in enantioenriched form, has been performed by Darzens-type reaction of lithiated chloroalkyloxazolines with benzotriazolylmethanol (BtCH(2)OH) or by chloromethylation of 2-acyl-2-oxazolines. The synthetic utility of such oxiranes based on their ability to act either as electrophiles, undergoing ring-opening reactions with nucleophiles, or as nucleophiles in form of the oxiranyl anions, generated by stereoselective beta-deprotonation, has been investigated. (C) 2009 Elsevier Ltd. All rights reserved
Iris type:
01.01 Articolo in rivista
List of contributors:
Cuocci, Corrado
Authors of the University:
CUOCCI CORRADO
Handle:
https://iris.cnr.it/handle/20.500.14243/160990
Published in:
TETRAHEDRON (OXF., PRINT)
Journal
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