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多氟代碳水化合物的合成与糖苷化。

The Synthesis and Glycoside Formation of Polyfluorinated Carbohydrates.

机构信息

School of Chemistry, University of Southampton, Highfield, Southampton, SO17 1BJ, U.K.

Department of Organic and Macromolecular Chemistry, Ghent University, Campus Sterre, Krijgslaan 281-S4, Ghent, 9000, Belgium.

出版信息

Chem Rev. 2022 Oct 26;122(20):15503-15602. doi: 10.1021/acs.chemrev.2c00086. Epub 2022 May 25.

Abstract

Fluorinated carbohydrates have found many applications in the glycosciences. Typically, these contain fluorination at a single position. There are not many applications involving polyfluorinated carbohydrates, here defined as monosaccharides in which more than one carbon has at least one fluorine substituent directly attached to it, with the notable exception of their use as mechanism-based inhibitors. The increasing attention to carbohydrate physical properties, especially around lipophilicity, has resulted in a surge of interest for this class of compounds. This review covers the considerable body of work toward the synthesis of polyfluorinated hexoses, pentoses, ketosugars, and aminosugars including sialic acids and nucleosides. An overview of the current state of the art of their glycosidation is also provided.

摘要

氟化碳水化合物在糖科学中有着广泛的应用。通常,这些化合物在一个位置进行氟化。涉及多氟化碳水化合物的应用并不多,这里将其定义为一个或多个碳原子上直接连接有至少一个氟取代基的单糖,除了将其用作基于机制的抑制剂外,这种应用很少见。人们对碳水化合物物理性质的关注度不断提高,特别是脂溶性方面,这导致人们对这类化合物产生了浓厚的兴趣。这篇综述涵盖了大量关于合成多氟化己糖、戊糖、酮糖和氨基糖(包括唾液酸和核苷)的工作。同时还概述了它们糖苷化的最新技术现状。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7c60/9615045/cd39ebe4861a/cr2c00086_0001.jpg

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