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-00000084.xml
Synthesis 1993; 1993(1): 72-74
DOI: 10.1055/s-1993-25798
DOI: 10.1055/s-1993-25798
short paper
© 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.
Acylation and Alkoxycarbonylation of Oximes Through an Enzymatic Oximolysis Reaction
Further Information
Publication History
Publication Date:
17 September 2002 (online)
Ketone or benzaldehyde O-acyloximes and O-(tert-butoxycarbonyl)oximes can be prepared by reaction of oximes with vinyl esters and di-tert-butyl dicarbonate, respectively, using lipases as biocatalysts.