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Highly Efficient and Regioselective Phosphorylation of Sphingolipids by Phase-Transfer Catalysis

机译:相转移催化高效鞘磷脂的区域选择性磷酸化

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摘要

Phosphorylation of D-erythro-sphingosine and its N-BOC or N-palmitoyl derivatives with trimethyl phosphite was carried out in 72-92% yield at room temperature for 20 min in a biphasic system comprised of dichloromethane/aqueous solutions of NaOH or K2CO3 using 1,2-dibromotetrachloroethane as a source of halogen and cetyl pyridinium bromide as a phase-transfer catalyst.These are the first reported examples of a highly selective O-and N-phosphorylation of sphingolipids by the phase-transfer catalysis.Our studies show that the developed phosphorylation protocol works as a modular process,in which the synthetic outcome is controlled by a type of the used base,catalyst and solvent system.
机译:在室温下,在由二氯甲烷/ NaOH或K2CO3水溶液组成的双相体系中,在室温下以72-92%的收率将D-赤型-鞘氨醇及其N-BOC或N-棕榈酰衍生物与亚磷酸三甲酯进行磷酸化20分钟。 1,2-二溴四氯乙烷是卤素的来源,而十六烷基溴化吡啶是相转移的催化剂,这是通过相转移催化对鞘脂进行高选择性O-和N-磷酸化的第一个报道实例。所开发的磷酸化方案是一个模块化过程,其中合成结果受所用碱,催化剂和溶剂系统类型的控制。

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