RSS-Feed abonnieren
Bitte kopieren Sie die angezeigte URL und fügen sie dann in Ihren RSS-Reader ein.
https://www.thieme-connect.de/rss/thieme/de/10.1055-s-00000084.xml
Synthesis 1987; 1987(8): 741-742
DOI: 10.1055/s-1987-28071
DOI: 10.1055/s-1987-28071
communication
© 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.
Oxidation von sec, sec-1,2-Diolen zu 1,2-Diketonen unter Pfitzner-Moffatt-Bedingungen
Weitere Informationen
Publikationsverlauf
Publikationsdatum:
12. September 2002 (online)

Oxidation of sec, sec-1,2-Diols to 1,2-Diketones under Pfitzner-Moffatt-Conditions In contrast to many other oxidation methods, the "Pfitzner-Moffatt" technique converts sec, sec-1,2-diols 1 into 1,2-diketones 2 without any C - C bond cleavage. Other functional groups like oletinic double bonds or esters are not affected under the mild and almost neutral reaction conditions.