Iron-Catalyzed Stereoselective Nitrogen Atom Transfer for 1,2-cis-Selective Glycosylation.

IF 1.4 4区 化学 Q3 CHEMISTRY, ORGANIC
Synlett Pub Date : 2025-08-20 DOI:10.1055/a-2654-5609
Hao Xu, Dakang Zhang, Zixiang Jiang, Le Yin, Spencer I Clark, Pinzhi Wang, Jordan D Lamar, Adam M Cohen
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引用次数: 0

Abstract

This account highlights an iron-catalyzed exclusively 1,2-cis-selective glycosylation method for aminoglycoside synthesis. This selective nitrogen atom transfer reaction is effective for a broad range of glycosyl donors and acceptors, and it can be operated in a reiterative fashion and scaled up to the multi-gram scale. Mechanistic studies revealed a unique yet generally applicable glycosylation mechanism in which the iron catalyst activates a glycosyl acceptor and an oxidant when it facilitates the cooperative atom transfer of both moieties to a glycosyl donor in an exclusively cis-selective manner.

铁催化的1,2-顺式选择性糖基化的立体选择性氮原子转移。
这个帐户强调了铁催化的专门1,2-顺式选择性糖基化方法氨基糖苷合成。这种选择性氮原子转移反应对广泛的糖基供体和受体有效,并且可以以重复的方式操作,并按比例扩大到多克尺度。机制研究揭示了一种独特但普遍适用的糖基化机制,其中铁催化剂激活糖基受体和氧化剂,当它以完全顺式选择的方式促进两个部分的糖基供体的协同原子转移。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Synlett
Synlett 化学-有机化学
CiteScore
3.40
自引率
5.00%
发文量
369
审稿时长
1 months
期刊介绍: SYNLETT is an international journal reporting research results and current trends in chemical synthesis in short personalized reviews and preliminary communications. It covers all fields of scientific endeavor that involve organic synthesis, including catalysis, organometallic, medicinal, biological, and photochemistry, but also related disciplines and offers the possibility to publish scientific primary data.
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