首页> 外文期刊>Indian Journal of Chemistry, Section B. Organic Including Medicinal >Solvent-free synthesis of 2',3',5'-tri-O-acetyl -2,6-dichloropurine nucleoside catalyzed by p-toluenesulfonic acid using microwave
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Solvent-free synthesis of 2',3',5'-tri-O-acetyl -2,6-dichloropurine nucleoside catalyzed by p-toluenesulfonic acid using microwave

机译:对甲苯磺酸微波催化无溶剂合成2',3',5'-三-O-乙酰基-2,6-二氯嘌呤核苷

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摘要

Starting from tetraacetylribofuranosc 1 and 2,6-dichloropurine 2,in the presence of p-toluenesulfonic acid (p-TsOH),2',3',5'-tri-O-acetyl-2,6-dichloropurine nucleoside 3 has been synthesized in microwave oven for the first time.On comparing(-> Comparing) with the conventional methods,this method has advantages such as shorter reaction time (4.5min),better yield (83.5%),simple(-> simpler) workup and environmental acceptability.
机译:在对甲苯磺酸(p-TsOH),2',3',5'-三-O-乙酰基-2,6-二氯嘌呤核苷3的存在下,从四乙酰基呋喃核糖1和2,6-二氯嘌呤2开始。与常规方法比较(->比较),该方法具有反应时间短(4.5min),收率高(83.5%),后处理简单(->更简单)和易于操作等优点。环境可接受性。

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