Aluminum trichloride-promoted aminolysis of cyclic imides and oxazolidinones

Aluminum trichloride promotes the nucleophilic ring-opening reaction of cyclic imides and oxazolidinones with amines. ω-Functionalized amides and urea are obtained in good to excellent yield by ring-opening reactions of cyclic imides and oxazolidinones.

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Bibliographic Details
Published in:Tetrahedron letters 1996-02, Vol.37 (8), p.1217-1220
Main Authors: Bon, Eric, Réau, Régis, Bertrand, Guy, Bigg, Dennis C.H
Format: Article
Language:English
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Description
Summary:Aluminum trichloride promotes the nucleophilic ring-opening reaction of cyclic imides and oxazolidinones with amines. ω-Functionalized amides and urea are obtained in good to excellent yield by ring-opening reactions of cyclic imides and oxazolidinones.
ISSN:0040-4039
1873-3581
DOI:10.1016/0040-4039(96)00003-2