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Synlett 1992; 1992(8): 643-645
DOI: 10.1055/s-1992-21441
DOI: 10.1055/s-1992-21441
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.
The Direct Conversion of Olefins into Esters Through Ozonolysis
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Publikationsverlauf
Publikationsdatum:
14. Dezember 2005 (online)
Ozonolysis of mono-, di- and trisubstituted olefins in 2.5 M methanolic sodium hydroxide-dichloromethane leads directly to methyl esters in high yield. For example, 3-benzyloxy-1-nonene (5b) was converted into methyl 2-benzyloxyoctanoate (7b) in 78% yield.