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Synthetic Studies toward the Natural Product Tripartin, the First Natural Histone Lysine Demethylase Inhibitor

机译:对天然产物Tripartin(第一种天然组蛋白赖氨酸脱甲基酶抑制剂)的合成研究

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An efficient synthesis of dimethyl tripartin as a synthetic precursor of natural product tripartin, the first natural specific inhibitor of histone H3 lysine 9 demethylase KDM4, is described. The synthesis of dimethyl tripartin was achieved in a six-step longest linear sequence starting from commercially available 3,5-dimethoxy benzaldehyde with 21% overall yield, using ClTi(OiPr)3-mediated dichloromethine insertion as the key step.
机译:描述了作为天然产物三甲酚(一种组蛋白H3赖氨酸9脱甲基酶KDM4的第一种天然特异性抑制剂)的合成前体的二甲三甲酚的有效合成。以ClTi(OiPr)3介导的二氯次甲基插入为关键步骤,从市售3,5-二甲氧基苯甲醛开始,以六步最长的线性顺序合成了二甲基三方丁酸酯,总产率为21%。

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