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Isolation and absolute configuration determination of alkaloids from Pandanus amaryllifolius

机译:Pandanus Amaryllifolius的分离和绝对构型测定生物碱的测定

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Seven new alkaloids belonging to three typical classes, isolated from an ethanolic extract of Pandanus amaryllifolius, were applied to establish the models in structural elucidation. The first type [pandanusines A and B (1 and 2)] was applied to alkaloids with a diazaspirocyclic ring system. The absolute stereo chemistry of aminal carbon is determined by analysis off-based configuration analysis and circular dichroism spectroscopy, which has never been revealed before. The second type [pandalizines C-E (3-5)], the stereochemistry of unusual indolizinone with chiral hydroxyl substitutions were determined by circular dichroism spectroscopy and vibrational circular dichroism experiments. The last type [norpandamarilactonines C and D (6 and 7)], a comparing model in determination of diastereomers of pyrrolidinyl alpha,beta-unsaturated I-lactone alkaloids was established. Our study provides solutions for a challenging subject in stereochemistry determination for three different types of Pandanus alkaloids. (C) 2017 Elsevier Ltd. All rights reserved.
机译:七种属于三种典型类的新生物碱,应用于与平原牛肉薄膜的乙醇提取物分离,以建立结构阐明的模型。第一种类型[Pandanisines A和B(1和2)]用具有DiazaspIriCyclic环系统的生物碱应用。芳链碳的绝对立体化学通过分析基于外部的配置分析和圆形二色性光谱来决定,从未透露过。通过圆形二色性光谱和振动圆形二色二倍态实验测定了第二种类型[熊甲嗪C-e(3-5)],异常吲哚啉酮的立体化学,具有手性羟基取代。最后一型[NoRPandamariLidonines C和D(6和7)],确定吡咯烷基亚α的非对映异构体的比较模型,建立了β-不饱和的I-内酯生物碱。我们的研究为三种不同类型的熊本生物碱进行了立体化学测定的具有挑战性的主体。 (c)2017 Elsevier Ltd.保留所有权利。

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