雪茄烟叶中的酮类化合物

IF 1.3 3区 医学 Q3 CHEMISTRY, APPLIED
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引用次数: 0

摘要

通过对雪茄烟叶进行植物化学研究,分离出了 18 种离子酮类化合物,其中包括以前未曾描述过的雪茄烟烷 E(1)和 F(2)。此外,还在烟叶中首次发现了醋酸 vomifoliol(3)、脱氢 vomifoliol(4)、8,9-二氢化雌甾-4,6-二烯-3-酮(5)、7α,8α-环氧布卢门醇 B(6)、3-oxoactinidol(12)和醋酸 loliolide(15)、4β-羟基二氢内酯(17)等化合物。通过严格的光谱分析,所有化合物的结构都得到了阐明。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Ionones from cigar tobacco leaves

Phytochemical studies on cigar tobacco leaves led to the isolation of 18 ionone-type compounds, including previously undescribed cigatobanes E (1) and F (2). Additionally, compounds vomifoliol acetate (3), dehydrovomifoliol (4), 8,9-dihydromegastigmane-4,6-diene-3-one (5), 7α,8α-epoxyblumenol B (6), 3-oxoactinidol (12), and loliolide acetate (15), 4β-hydroxy-dihydroactinidiolide (17), were found in tobacco leaves for the first time. The structural elucidation of all compounds was accomplished through rigorous spectral analysis.

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来源期刊
CiteScore
3.20
自引率
5.90%
发文量
47
审稿时长
2.3 months
期刊介绍: The Journal of Asian Natural Products Research (JANPR) publishes chemical and pharmaceutical studies in the English language in the field of natural product research on Asian ethnic medicine. The journal publishes work from scientists in Asian countries, e.g. China, Japan, Korea and India, including contributions from other countries concerning natural products of Asia. The journal is chemistry-orientated. Major fields covered are: isolation and structural elucidation of natural constituents (including those for non-medical uses), synthesis and transformation (including biosynthesis and biotransformation) of natural products, pharmacognosy, and allied topics. Biological evaluation of crude extracts are acceptable only as supporting data for pure isolates with well-characterized structures. All published research articles in this journal have undergone rigorous peer review, based on initial editor screening and anonymized refereeing by at least two expert referees.
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