Synlett 1993; 1993(7): 511-512
DOI: 10.1055/s-1993-22511
letter
© Georg Thieme Verlag, Rüdigerstr. 14, 70469 Stuttgart, Germany. All rights reserved. This journal, including all individual contributions and illustrations published therein, is legally protected by copyright for the duration of the copyright period. Any use, exploitation or commercialization outside the narrow limits set by copyright legislation, without the publisher's consent, is illegal and liable to criminal prosecution. This applies in particular to photostat reproduction, copying, cyclostyling, mimeographing or duplication of any kind, translating, preparation of microfilms, and electronic data processing and storage.

Synthesis of Unsymmetrical α-Diketones via Autooxidation of α-Hydroxy Imines

Masahiro Murakami* , Ichiro Komoto, Hajime Ito, Yoshihiko Ito
  • *Department of Synthetic Chemistry, Faculty of Engineering, Kyoto University, Yoshida, Kyoto 606-01, Japan
Further Information

Publication History

Publication Date:
19 March 2002 (online)

A new method for the synthesis of unsymmetrical αdiketones is developed. Autoxidation of α-hydroxy imines, prepared by samarium(II) iodide-mediated three-component coupling of an organic halide, 2,6-xylyl isocyanide, and a carbonyl compound, afforded the corresponding α-keto imines, which were hydrolyzed to α-diketones in high yield.

    >