首页> 外文期刊>Australian Journal of Chemistry: A Journal for the Publication of Original Research in All Branches of Chemistry >Septanose carbohydrates. VII. Preparation of mono-O-isopropylidene derivatives of methyl #beta#-D-glucoseptanoside and preparation of methyl #alpha#- L-idoseptanoside and its derivatives
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Septanose carbohydrates. VII. Preparation of mono-O-isopropylidene derivatives of methyl #beta#-D-glucoseptanoside and preparation of methyl #alpha#- L-idoseptanoside and its derivatives

机译:琼脂糖碳水化合物。七。甲基#β#-D-葡庚糖苷的单-O-异亚丙基衍生物的制备和甲基#α#-L-异庚糖苷及其衍生物的制备

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摘要

Three mono-O-isopropylidene derivatives of methyl #beta#-D-glucoseptanoside have been prepared by acid-catalysed hydrolysis of methyl 2,3:4,5-di-O-isopropylidene-#beta#-D-glucoseptanoside or by acetonation of methyl #beta#-D-glucoseptanoside. Two of these derivatives have been used for the preparation of methyl 2,3-O-isopropylidene-#alpha#-L-idoseptanoside (8a) and methyl 3,4-O-isopropylidene-#alpha#-L-idoseptanoside (10a). Hydrolysis of (10a) yielded methyl #alpha#-L-idoseptanoside (12a) and acetonation of (8a) and (12a) yielded methyl 2,3:4,5-di-O-isopropylidene-#alpha#-L-idoseptanoside. Possible conformations of these compounds are discussed.
机译:通过酸催化甲基2,3:4,5-二-O-异亚丙基-#β#-D-葡糖庚糖苷的水解或通过丙酮化制备了甲基#beta#-D-葡糖苷的三种单-O-异亚丙基衍生物甲基#β#-D-葡萄糖苷。这些衍生物中的两种已用于制备甲基2,3-O-异亚丙基-#alpha#-L-异庚糖苷(8a)和甲基3,4-O-异亚丙基-#alpha#-L-异庚糖苷(10a) 。 (10a)的水解产生甲基#α#-L-异庚糖苷(12a),并且丙酮化(8a)和(12a)产生甲基2,3:4,5-二-O-异亚丙基-#alpha#-L-异庚糖苷。讨论了这些化合物的可能构象。

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