Click Reactions as a Key Step for an Efficient and Selective Synthesis of D-Xylose-Based ILs

Nadège Ferlin; Sylvain Gatard; Albert Nguyen van Nhien; Matthieu Courty; Sandrine Bouquillon

doi:10.3390/molecules180911512

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Click Reactions as a Key Step for an Efficient and Selective Synthesis of D-Xylose-Based ILs

Journal article

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Click Reactions as a Key Step for an Efficient and Selective Synthesis of D-Xylose-Based ILs

Nadège Ferlin, Sylvain Gatard, Albert Nguyen van Nhien, Matthieu Courty and Sandrine Bouquillon

Molecules, Vol.18(9), pp.11512-11525

2013

DOI: https://doi.org/10.3390/molecules180911512

PMCID: PMC6270402

Abstract

ionic liquids

D-xylose

click chemistry

D-Xylose-based ionic liquids have been prepared from D-xylose following a five steps reaction sequence, the key step being a click cycloaddition. These ionic liquids (ILs) have been characterized through classical analytical methods (IR, NMR, mass spectroscopy, elemental analysis) and their stability constants, Tg and Tdec, were also determined. Considering their properties and their hydrophilicity, these compounds could be alternative solvents for chemical applications under mild conditions.

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Title: Click Reactions as a Key Step for an Efficient and Selective Synthesis of D-Xylose-Based ILs
Creators - without role: Nadège Ferlin - Institut de Chimie Moléculaire de Reims
Sylvain Gatard - Centre National de la Recherche Scientifique
Albert Nguyen van Nhien - Laboratoire des Glucides
Matthieu Courty - Université de Picardie Jules Verne
Sandrine Bouquillon - Université de Reims Champagne-Ardenne
Publication Details: Molecules, Vol.18(9), pp.11512-11525
Identifiers: 9940879909311
Academic Unit: Université de Montpellier
Language: English
Resource Type: Journal article
Local Fields: hal-02540468