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Recent trends in the synthesis of O-glycosides of 2-amino-2-deoxysugars

机译:2-氨基-2-脱氧糖的O-糖苷合成的最新趋势

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摘要

The discovery of new methods for stereoselective glycoside synthesis and convergent oligosaccharide assembly has been critical for the area of glycosciences. At the heart of this account is the discussion of the approaches for stereoselective synthesis of glycosides of 2-amino-2-deoxysugars that have emerged during the past two decades. The introductory part provides general background information and describes the key features and challenges for the synthesis of this class of compounds. Subsequently, major approaches to the synthesis of 2-amino-2-deoxyglycosides are categorized and discussed. Each subsection elaborates on the introduction (or protection) of the amino functionality, synthesis of glycosyl donors by introduction of a suitable leaving group, and glycosidation. Wherever applicable, the deprotection of a temporary amino group substituent and the conversion onto the natural acetamido functionality is described. The conclusions part evaluates the current standing in the field and provides a perspective for future developments. (c) 2006 Elsevier Ltd. All rights reserved.
机译:立体选择性糖苷合成和聚合寡糖组装新方法的发现对于糖科学领域至关重要。该论述的核心是对过去二十年来出现的2-氨基-2-脱氧糖糖苷的立体选择性合成方法的讨论。引言部分提供了一般的背景信息,并描述了此类化合物合成的关键特征和挑战。随后,归纳和讨论了合成2-氨基-2-脱氧糖苷的主要方法。每个小节详细介绍了氨基官能团的引入(或保护),通过引入合适的离去基团进行糖基供体的合成以及糖基化。在适当的地方,描述了临时氨基取代基的脱保护和天然乙酰胺官能团的转化。结论部分评估了该领域的现状,并为未来的发展提供了前景。 (c)2006 Elsevier Ltd.保留所有权利。

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