首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Synthesis of (-)-N-Acetylslaframine by C-1, C-5 Bis-hydroxyalkylation of (S)-2-(N,N-Dibenzylamino)-1,5-pentanediol via Highly Diastereoselective Lithiation of the Dicarbamate
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Synthesis of (-)-N-Acetylslaframine by C-1, C-5 Bis-hydroxyalkylation of (S)-2-(N,N-Dibenzylamino)-1,5-pentanediol via Highly Diastereoselective Lithiation of the Dicarbamate

机译:(S)-2-(N,N-二苄氨基)-1,5-戊二醇的C-1,C-5双羟基烷基化反应通过二氨基甲酸酯的高度非对映选择性合成来合成(-)-N-乙酰基草胺

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摘要

(-)-N-Acetylslaframine, a stable form of the indolizidine alkaloid (-)-slaframine, has been synthesised by a new strategy. Applying highly stereoselective lithiation and substitution reactions, C-2, C-3 and C-8 of the bicyclic skeleton were introduced to an l-glutamic acid derived diol dicarbamate.
机译:(-)-N-乙酰基草胺,一种稳定形式的吲哚并立生物碱(-)-草酸胺,已通过一种新策略合成。通过进行高度立体选择性的锂化和取代反应,将双环骨架的C-2,C-3和C-8引入L-谷氨酸衍生的二醇二氨基甲酸酯。

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