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Studies toward Synthesis of Arteminolides: Intramolecular [5+2] Oxidopyrylium Ion Cycloaddition Reactions with Silicon Tether

机译:合成蒿甲内酯的研究:分子内[5 + 2]氧吡啶鎓离子与硅系链的环加成反应

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摘要

Arteminolides A-D (1-4) are sesquiterpene lactones isolated from the leaves of Artemisia sylvatica Maxim and have been reported to be the strongest inhibitors of farnesyltransferase (FTase) with good selectivity from natural sources. While the biological profile and structural complexity of these natural products are intriguing, there has been no report on the synthesis of these natural products since their first isolation in 1998.
机译:青蒿内酯A-D(1-4)是从青蒿(Artemisia sylvatica Maxim)的叶子中分离得到的倍半萜内酯,据报道是对法呢基转移酶(FTase)的最强抑制剂,具有很好的天然来源选择性。尽管这些天然产物的生物学特性和结构复杂性令人着迷,但自1998年首次分离以来,没有关于这些天然产物合成的报道。

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