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1H and 13C NMR signal assignments of a novel Baeyer–Villiger originated diterpene lactone

✍ Scribed by Henriete S. Vieira; Jacqueline A. Takahashi; A. A. Leslie Gunatilaka; Maria Amélia D. Boaventura

Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
127 KB
Volume
44
Category
Article
ISSN
0749-1581

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✦ Synopsis

A highly rearranged novel dilactone was the single product isolated from Baeyer-Villiger oxidation of a norketone prepared from grandiflorenic acid, a natural kaurane diterpene. The complete 1H and 13C NMR assignment is presented for this novel compound that showed discrete in vitro antibacterial activity.

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