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三氯化铁作为一种高效的手性催化剂用于糖基叠氮化物的立体选择性合成,以及与 Cu(0) 作为共催化剂用于后续的点击化学反应。

Iron(III) chloride as an efficient catalyst for stereoselective synthesis of glycosyl azides and a cocatalyst with Cu(0) for the subsequent click chemistry.

机构信息

Department of Chemistry, National Taiwan Normal University, Taipei, Taiwan.

出版信息

Chem Commun (Camb). 2011 Oct 7;47(37):10440-2. doi: 10.1039/c1cc13370e. Epub 2011 Aug 15.

Abstract

A highly efficient and mild method for azido glycosylation of glycosyl β-peracetates to 1,2-trans glycosyl azides was developed by using inexpensive FeCl(3) as the catalyst. In addition, we demonstrated, for the first time, that FeCl(3) in combination with copper powder can promote 1,3-dipolar cycloaddition (click chemistry) of azido glycosides with terminal alkynes. Good to excellent yields were obtained with exclusive formation of a single isomer in both glycosyl azidation and subsequent cycloaddition processes.

摘要

一种高效温和的方法,通过使用廉价的三氯化铁作为催化剂,将糖基β-醋酸酯进行叠氮糖苷化,生成 1,2-反式糖基叠氮化物。此外,我们首次证明,三氯化铁与铜粉结合可以促进端炔与叠氮糖的 1,3-偶极环加成(点击化学)。在糖基叠氮化和随后的环加成过程中,均以单一异构体的形式得到了良好至优秀的产率。

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