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一条通往具有生物学意义的吡喃查耳酮天然产物的高效快速合成路线。

An efficient and rapid synthetic route to biologically interesting pyranochalcone natural products.

作者信息

Lee Yong Rok, Wang Xue, Xia Likai

机构信息

School of Chemical Engineering and Technology, Yeungnam University, Gyeongsan 712-749, Korea.

出版信息

Molecules. 2007 Jul 12;12(7):1420-9. doi: 10.3390/12071420.

DOI:10.3390/12071420
PMID:17909497
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6149329/
Abstract

An efficient and concise total synthesis of naturally occurring pyranochalcones was achieved from readily available 2,4-dihydroxyacetophenone and 2,4-dihydroxy-6-methoxyacetophenone. The key steps in the synthetic strategy were ethylenediamine diacetate-catalyzed benzopyran formation and aldol reactions.

摘要

以易得的2,4-二羟基苯乙酮和2,4-二羟基-6-甲氧基苯乙酮为原料,实现了天然存在的吡喃查耳酮的高效简洁全合成。合成策略中的关键步骤是乙二胺二乙酸酯催化的苯并吡喃形成反应和羟醛缩合反应。

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本文引用的文献

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Prenylated flavonoids from the heartwood of Artocarpus communis with inhibitory activity on lipopolysaccharide-induced nitric oxide production.来自面包树心材的异戊烯基黄酮对脂多糖诱导的一氧化氮产生具有抑制活性。
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A new 5-lipoxygenase selective inhibitor derived from Artocarpus communis strongly inhibits arachidonic acid-induced ear edema.一种源自面包树的新型5-脂氧合酶选择性抑制剂能强烈抑制花生四烯酸诱导的耳部水肿。
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