Conversion of glycals into vicinal-1,2-diazides and 1,2-(or 2,1)-azidoacetates using hypervalent iodine reagents and Me3SiN3. Application in the synthesis of: N -glycopeptides, pseudo-trisaccharides and an iminosugar

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Abstract

Glycals were found to react with a reagent system comprising of phenyliodine bis(trifluoroacetate) (PIFA) and Me3SiN3 in the presence of TMSOTf as a catalyst to form the corresponding vicinal 1,2-diazides. On the other hand, they reacted with another reagent system phenyliodine diacetate (PIDA) and Me3SiN3, also in the presence of TMSOTf as a catalyst, to lead to the corresponding vicinal 1,2-azidoacetates. These azido derivatives were converted into a number of 2-azido-N-glycopeptides, pseudotrisaccharides, and a piperidine triol derivative, an iminosugar.

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Chennaiah, A., Bhowmick, S., & Vankar, Y. D. (2017). Conversion of glycals into vicinal-1,2-diazides and 1,2-(or 2,1)-azidoacetates using hypervalent iodine reagents and Me3SiN3. Application in the synthesis of: N -glycopeptides, pseudo-trisaccharides and an iminosugar. RSC Advances, 7(66), 41755–41762. https://doi.org/10.1039/c7ra08637g

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