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A direct synthetic approach to uracil anhydrothionucleoside derivatives

机译:尿嘧啶脱水硫代核苷衍生物的直接合成方法

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摘要

Direct conversion of peracylated N-1-(beta-D-glucopyranosyl)-2-thiouracil derivatives into the corresponding anhydrothionucleosides has been studied under various conditions including: gas-phase pyrolysis, heating without a solvent, and by heating in a solvent of high boiling point (DPE) in the presence of a base (DABCO) and reaction in a microwave reactor. Heating at 210-220 degrees C was found to give the best yield of a single isomer. The structures of the new anhydrothionucleosides were confirmed by NMR techniques
机译:已研究了在各种条件下将过酰化的N-1-(β-D-吡喃葡萄糖基)-2-硫尿嘧啶衍生物直接转化为相应的脱水硫核苷的方法,包括:气相热解,无溶剂加热以及在高溶剂中加热碱(DABCO)存在下的沸点(DPE),并在微波反应器中进行反应。发现在210-220℃加热可得到单一异构体的最佳产率。新的脱水硫代核苷的结构已通过NMR技术确认

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