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Structure assignment by 1H and 13C NMR of two epimers derived from glycyrrhetic acid

✍ Scribed by Alessandro Bongini; Michele Contento; Mario Orena; Giorgio Pifferi; Roberto Erba


Publisher
John Wiley and Sons
Year
1984
Tongue
English
Weight
153 KB
Volume
22
Category
Article
ISSN
0749-1581

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✦ Synopsis


A full assignment of the 13C signals of four pentacyclic triterpenes confirms the results obtained by 'H NMR analysis of steroidal methyls, resolving the stereochemistry of the oxidation product of 3-~-acetoxyolean-12-en-30-oic acid methyl ester.


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