一种高效合成羊角苷的新方法

IF 1.8 3区 化学 Q3 CHEMISTRY, ORGANIC
Wenpei Zhang (Data curation Investigation Methodology Writing – original draft Writing – review & editing) , Xinyue Pan (Investigation) , Jie He (Supervision) , Yirong Lin (Visualization) , Fengyang Zhang (Validation) , Li Guo (Validation) , Jieqing Liu (Conceptualization Funding acquisition Project administration Resources)
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引用次数: 0

摘要

Erianin是一种在石斛中发现的天然联苯化合物,具有显著的抗肿瘤和抗炎作用。本文报道了一种以纯香草酸和3,4,5-三甲氧基苯甲醛为原料,三步合成Erianin的新方法。我们的方法集成了羟基醛缩合、微波辅助脱羧和温和的双键还原,总收率为45.3%,比以前的方法提高了47.7%。开发的方案为获得Erianin提供了一种具有成本效益和可扩展的方法,为治疗研究和药物开发提供了巨大潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A novel strategy for the efficient synthesis of Erianin
Erianin, a natural biphenyl compound found in Dendrobium, exhibits significant pharmacological effects, including anti-tumor and anti-inflammatory properties. Here, we report a novel and efficient three-step synthetic route for Erianin, utilizing homovanillic acid and 3,4,5-trimethoxybenzaldehyde as starting materials. Our method integrates hydroxyaldehyde condensation, microwave-assisted decarboxylation, and mild double bond reduction, achieving a total yield of 45.3%—a 47.7% improvement over prior approaches. The developed protocol provides a cost-effective and scalable approach to access Erianin, offering significant potential for therapeutic research and drug development.
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来源期刊
Synthetic Communications
Synthetic Communications 化学-有机化学
CiteScore
4.40
自引率
4.80%
发文量
156
审稿时长
4.3 months
期刊介绍: Synthetic Communications presents communications describing new methods, reagents, and other synthetic work pertaining to organic chemistry with sufficient experimental detail to permit reported reactions to be repeated by a chemist reasonably skilled in the art. In addition, the Journal features short, focused review articles discussing topics within its remit of synthetic organic chemistry.
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