Subscribe to RSS
Please copy the URL and add it into your RSS Feed Reader.
https://www.thieme-connect.de/rss/thieme/en/10.1055-s-00000083.xml
Synlett 1993; 1993(7): 511-512
DOI: 10.1055/s-1993-22511
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
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.