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首页> 外文期刊>Carbohydrate research >Glycerol carbonate in Ferrier reaction: Access to new enantiopure building blocks to develop glycoglycerolipid analogues
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Glycerol carbonate in Ferrier reaction: Access to new enantiopure building blocks to develop glycoglycerolipid analogues

机译:Ferrier反应中的碳酸甘油酯:获得新的对映纯构件以开发甘油甘油脂类似物

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摘要

Glycerol carbonate and tri-O-acetyl-D-glucal were used for the synthesis of glycero-functionalized carbohydrates. Ferrier reaction between the two partners afforded the O-glucoside in 84% yield. Spontaneous crystallization yielded 28% of a pure diastereoisomer with the S configuration as determined by X-ray crystallography. Then, the azido-glycerosugar was prepared in two steps: ring opening of the cyclic carbonate with sodium azide and per-acetylation with an excellent yield of 94%. A library of glyco-conjugates were prepared using a 1,3-dipolar cycloaddition in yields ranging from 64 to 99%. (C) 2016 Elsevier Ltd. All rights reserved.
机译:碳酸甘油酯和三-O-乙酰基-D-葡糖醛被用于甘油官能化碳水化合物的合成。两种伙伴之间的加重反应以84%的产率提供了O-葡萄糖苷。通过X射线晶体学测定,自发结晶产生具有S构型的纯非对映异构体的28%。然后,分两步制备叠氮基-甘油糖:用叠氮化钠使环状碳酸酯开环和过乙酰化,产率高达94%。使用1,3-偶极环加成制备了糖缀合物库,产率为64%至99%。 (C)2016 Elsevier Ltd.保留所有权利。

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