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

被引:1
作者
dos Santos, Carlos Henrique Totini [1 ]
Petrica, Edith Eunice Arthur [1 ]
de Luca Batista, Andrea Nastri [2 ]
Rodrigues, Edilene Delphino [1 ]
Garcez, Walmir Silva [1 ]
de Albuquerque, Ana Carolina Ferreira [2 ]
dos Santos Jr, Fernando Martins [2 ]
Batista Jr, Joao Marcos [3 ]
Garcez, Fernanda Rodrigues [1 ]
机构
[1] Univ Fed Mato Grosso do Sul, Inst Chem, BR-79074460 Campo Grande, MS, Brazil
[2] Fluminense Fed Univ, Inst Chem, BR-24020141 Niteroi, RJ, Brazil
[3] Univ Fed Sao Paulo, Inst Sci & Technol, BR-12231280 Sao Jose Dos Campos, SP, Brazil
来源
JOURNAL OF NATURAL PRODUCTS | 2024年 / 87卷 / 03期
基金
巴西圣保罗研究基金会;
关键词
BRAZILIAN LAURACEAE; NATURAL-PRODUCTS; CHEMISTRY; OCOBULLENONE; LEAVES;
D O I
10.1021/acs.jnatprod.3c01013
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
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.
引用
收藏
页码:456 / 469
页数:14
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