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首页> 外文期刊>Heterocycles: An International Journal for Reviews and Communications in Heterocyclic Chemistry >IMPROVED SYNTHESES OF D-RIBO- AND 2-DEOXY-D-RIBOFURANOSE PHOSPHO SUGARS FROM METHYL P-D-RIBOPYRANOSIDE
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IMPROVED SYNTHESES OF D-RIBO- AND 2-DEOXY-D-RIBOFURANOSE PHOSPHO SUGARS FROM METHYL P-D-RIBOPYRANOSIDE

机译:由甲基对-D-核糖吡喃糖苷合成D-核糖和2-脱氧-D-核糖呋喃糖磷酸糖

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摘要

Methyl 4-deoxy-4-dimethoxyphosphinoyl-2,3-O-isopropylidene-beta-D-ribopyranoside (12a) and methyl 2,4-dideoxy-4-dimethoxyphosphinoyl-beta-D-erythro-pentopyranoside (20) were efficiently prepared respectively from methyl 2,3-O-isopropylidene-beta-D-ribopyranoside (7a) and its 3,4-O-isopropylidene isomer (7b) in appreciably improved total yields compared with those via previously reported routes.Compounds (12a,20) were led to D-ribofuranose and 2-deoxy-D-ribofuranose phospho sugars (4,5).
机译:有效地制备了4-脱氧-4-二甲氧基膦酰基-2,3-O-异亚丙基-β-D-核吡喃糖苷(12a)和2,4-二脱氧-4-二甲氧基膦酰基-β-D-赤型-戊吡喃糖苷(20)。分别来自甲基2,3-O-异亚丙基-β-D-核吡喃糖苷(7a)及其3,4-O-异亚丙基异构体(7b)的总收率与先前报道的路线相比明显提高。化合物(12a,20 )产生D-核呋喃糖和2-脱氧-D-呋喃糖磷酸糖(4,5)。

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