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首页> 外文期刊>Tetrahedron letters: The International Journal for the Rapid Publication of Preliminary Communications in Organic Chemistry >A tethered aminohydroxylation route to L-arabino-[2R,3S,4R] and L-xylo-[2R,3S,4S]-C_(18)-phytosphingosines
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A tethered aminohydroxylation route to L-arabino-[2R,3S,4R] and L-xylo-[2R,3S,4S]-C_(18)-phytosphingosines

机译:L-阿拉伯糖-[2R,3S,4R]和L-木糖-[2R,3S,4S] -C_(18)-植物鞘氨醇的束缚氨基羟基化途径

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摘要

A concise and highly efficient synthesis of L-arabino-[2R,3S,4R] and L-xylo-[2R,3S,4S]-C_(18)-phytosphingo-sines has been achieved. The synthetic strategy features the Sharpless kinetic resolution and tethered aminohydroxylation as the key steps.
机译:L-阿拉伯糖-[2R,3S,4R]和L-木糖-[2R,3S,4S] -C_(18)-植物鞘氨醇的简明高效合成方法已实现。合成策略以Sharpless动力学拆分和束缚的氨基羟基化为关键步骤。

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