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Transformation of hex-2-enopyranosyl trichloroacetimidates - a correction
Authors:Ingolf Dyong  Hans Merten  Joachim Thiem
Affiliation:Organisch-Chemisches Institut der Universität Münster, Orléans-Ring 23, D-4400 Munster, Federal Republic of Germany
Abstract:Contrary to previous results hex-2-enopyranosyl trichloroacetimidates do not rearrange to amino-branched glycals but give N-acylated hex-2-enopyranosyl amines.
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