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首页> 外文期刊>Journal of natural products >Efficient Synthesis of Cannabigerol, Grifolin, and Piperogalin via Alumina-Promoted Allylation
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Efficient Synthesis of Cannabigerol, Grifolin, and Piperogalin via Alumina-Promoted Allylation

机译:通过氧化铝 - 促进的烯丙基化高效合成Cannabigerol,Grifolin和Piperogalin

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摘要

The synthesis of three phenolic natural products has been accomplished with unprecedented efficiency using a new alumina-promoted regioselective aromatic allylation reaction. Cannabigerol and grifolin were prepared in one step from the inexpensive 5-alkyl-resorcinols olivetol and orcinol. Piperogalin was synthesized, for the first time, via two sequential allylations of orcinol with geraniol and prenol.
机译:使用新的氧化铝促进的区域选择性芳族烯丙基化反应来实现三种酚类天然产物的合成以前所未有的效率完成。 在从廉价的5-烷基 - 间苯醇olivetol和Orcinol中,在一步中制备Cannabigerol和Grifolin。 首次通过用Geraniol和Prenol的两种顺序烯醇合成哌啶醇素。

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