Application of the Suzuki-Miyaura reaction in the synthesis of flavonoids.

Application of the Suzuki-Miyaura reaction in the synthesis of flavonoids.
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铃木 - 米洛拉反应在类黄酮的合成中的应用。

DOI:
10.3390/molecules18044739
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发表时间:
2013-04-22
期刊:
Molecules (Basel, Switzerland)
影响因子:
--
通讯作者:
Van Heerden FR
Van Heerden FR
中科院分区:
其他
文献类型:
--
作者:
Selepe MA;Van Heerden FR

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综述了Suzuki-Miyaura反应在天然产物黄酮类化合物合成中的应用。该反应不仅被用于提供类黄酮核的通路,而且还被应用于二聚类黄酮的合成和用于生物活性研究的类黄酮衍生物库的合成。类黄酮的讨论是查耳酮,黄酮,异黄酮,奈替尼酮,双黄酮和衍生物的类黄酮通过C-C键形成通过铃木-宫浦反应。
The application of the Suzuki-Miyaura reaction in the synthesis of flavonoids, an important class of natural products, is reviewed. This reaction has not only been employed to provide access to flavonoid nuclei, but has also been applied to the synthesis of dimeric flavonoids and in the synthesis of libraries of flavonoid derivatives for biological activity studies. The classes of flavonoids that are discussed are the chalcones, flavones, isoflavones, neoflavones, biflavones and derivatives of flavonoids obtained by C-C bond formation via the Suzuki-Miyaura reaction.
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发表时间: 1996-11-07
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