Efficient and selective azidation of per-O-acetylated sugars using ultrasound activation: application to the one-pot synthesis of 1,2,3-triazole glycosides-Reference-Cited by-同舟云学术

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

Published:2015 Issue:7 Volume:39 Page:5437-5444
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Marzag Hamid¹²³⁴⁵,Alaoui Soukaina⁵⁶⁷⁸⁹,Amdouni Hella¹²³⁴,Martin Anthony R.¹²³⁴,Bougrin Khalid⁵⁶⁷⁸⁹,Benhida Rachid¹²³⁴

Affiliation:

1. Institut de Chimie de Nice UMR UNS-CNRS 7272

2. Université Nice Sophia Antipolis

3. 06108 Nice Cedex 2

4. France

5. Laboratoire de Chimie des Plantes et de Synthèse Organique et Bioorganique

6. URAC23

7. Université Mohammed V

8. Faculté des Sciences

9. B.P. 1014 Rabat

Abstract

A new protocol was developed for the selective transformation of acetyl-sugars to triazolyl nucleosides using in situ generated SO₂(N₃)₂, iron/copper cocatalysis and ultrasound activation.

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2015/NJ/C5NJ00624D

Reference52 articles.

1. Recent advances in the synthesis of functionalized carbohydrate azides

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3. Organic Azides: An Exploding Diversity of a Unique Class of Compounds

4. Cu-Catalyzed Azide−Alkyne Cycloaddition

5. Sonochemistry: A Powerful Way of Enhancing the Efficiency of Carbohydrate Synthesis

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