Issue 37, 2011

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

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 FeCl3 as the catalyst. In addition, we demonstrated, for the first time, that FeCl3 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.

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

Supplementary files

Article information

Article type
Communication
Submitted
07 Jun 2011
Accepted
26 Jul 2011
First published
15 Aug 2011

Chem. Commun., 2011,47, 10440-10442

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

S. B. Salunke, N. S. Babu and C. Chen, Chem. Commun., 2011, 47, 10440 DOI: 10.1039/C1CC13370E

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