Efficient and selective azidation of per-O-acetylated sugars using ultrasound activation: application to the one-pot synthesis of 1,2,3-triazole glycosides

Hamid Marzag; Soukaina Alaoui; Hella Amdouni; Anthony Martin; Khalid Bougrin; Rachid Benhida

doi:10.1039/C5NJ00624D

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Efficient and selective azidation of per-O-acetylated sugars using ultrasound activation: application to the one-pot synthesis of 1,2,3-triazole glycosides

Journal article

Peer reviewed

Efficient and selective azidation of per-O-acetylated sugars using ultrasound activation: application to the one-pot synthesis of 1,2,3-triazole glycosides

Hamid Marzag, Soukaina Alaoui, Hella Amdouni, Anthony Martin, Khalid Bougrin and Rachid Benhida

New Journal of Chemistry, Vol.39(7), pp.5437-5444

2015

DOI: https://doi.org/10.1039/C5NJ00624D

Abstract

A new protocol was developed for the selective transformation of acetyl-sugars to triazolyl nucleosides using in situ generated SO 2 (N 3 ) 2 , iron/copper cocatalysis and ultrasound activation.

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Title: Efficient and selective azidation of per-O-acetylated sugars using ultrasound activation: application to the one-pot synthesis of 1,2,3-triazole glycosides
Creators - without role: Hamid Marzag - Institut de Chimie de Nice
Soukaina Alaoui - Mohammed V University
Hella Amdouni - Université Côte d'Azur
Anthony Martin - Université de Montpellier, Institut des Biomolécules Max Mousseron - IBMM
Khalid Bougrin - Mohammed V University
Rachid Benhida - Institut de Chimie de Nice
Publication Details: New Journal of Chemistry, Vol.39(7), pp.5437-5444
Identifiers: 9946768809311
Academic Unit: Institut des Biomolécules Max Mousseron - IBMM
Language: English
Resource Type: Journal article
Local Fields: hal-04599376