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Esters of jasmorange oxime

Esters of jasmorange oxime The aldehyde jasmorange (1) was converted to the oxime (2), acylation of which by alkylcarboxylic acid anhydrides in the presence of HClO4 or by acid chlorides in the presence of pyridine synthesized esters of jasmorange oxime 3–24 in 82–91% yields. Refluxing 3–24 in hexane converted them quantitatively into nitrile 25. http://www.deepdyve.com/assets/images/DeepDyve-Logo-lg.png Chemistry of Natural Compounds Springer Journals

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References (2)

Publisher
Springer Journals
Copyright
Copyright © 2007 by Springer Science+Business Media, Inc.
Subject
Pharmacy; Pharmacy; Organic Chemistry; Plant Sciences
ISSN
0009-3130
eISSN
1573-8388
DOI
10.1007/s10600-007-0140-z
Publisher site
See Article on Publisher Site

Abstract

The aldehyde jasmorange (1) was converted to the oxime (2), acylation of which by alkylcarboxylic acid anhydrides in the presence of HClO4 or by acid chlorides in the presence of pyridine synthesized esters of jasmorange oxime 3–24 in 82–91% yields. Refluxing 3–24 in hexane converted them quantitatively into nitrile 25.

Journal

Chemistry of Natural CompoundsSpringer Journals

Published: Nov 9, 2007

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