7.1',8.3'- and 7.3',8.5'-Connected Bicyclo[3.2.1]octanoids and Oxabicyclo[3.2.2]nonane-Type Neolignans from Ocotea aciphylla : Structures and Absolute Configurations.
Carlos Henrique Totini Dos SantosEdith Eunice Arthur PetricaAndrea N L BatistaEdilene Delphino RodriguesWalmir Silva GarcezAna Carolina Ferreira de AlbuquerqueFernando Martins Dos Santos JuniorJoão Marcos BatistaFernanda Rodrigues GarcezPublished in: Journal of natural products (2024)
The phytochemical investigation of the leaves and trunk bark of a specimen of Ocotea aciphylla collected in the southern portion of the Amazon forest led to the isolation of an oxabicyclo[3.2.2]nonane-type neolignan and 15 bicyclo[3.2.1]octanoid neolignans, 14 of which are unreported compounds ( 2 - 15 ), including one with an unusual oxidation pattern of the side chain at C-1' and two rare 7.1',8.3'-connected bicyclo[3.2.1]octanoid derivatives. Their structures and relative configurations were determined by extensive spectrometric analysis based on 1D- and 2D-NMR spectroscopy and HRESIMS data, while their absolute configurations were unambiguously assigned using electronic and vibrational circular dichroism data assisted by density functional theory calculations. Additionally, known sesquiterpenes, phenylpropanoids, and phytosterols were also isolated.
Keyphrases
- density functional theory
- molecular dynamics
- electronic health record
- high resolution
- big data
- climate change
- molecular dynamics simulations
- hydrogen peroxide
- liquid chromatography
- machine learning
- mass spectrometry
- nitric oxide
- high performance liquid chromatography
- gas chromatography
- structure activity relationship
- essential oil