| Literature DB >> 16358289 |
Henriete S Vieira1, Jacqueline A Takahashi, A A Leslie Gunatilaka, Maria Amélia D Boaventura.
Abstract
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. Copyright 2005 John Wiley & Sons, Ltd.Entities:
Mesh：
Substances：
Year: 2006 PMID： 16358289 DOI： 10.1002/mrc.1738
Source DB: PubMed Journal: Magn Reson Chem ISSN： 0749-1581 Impact factor: 2.447