International Journal of the Biology, Chemistry, Physics, and Technology of Wood
Editor-in-Chief: Faix, Oskar
Editorial Board: Daniel, Geoffrey / Militz, Holger / Rosenau, Thomas / Salmen, Lennart / Sixta, Herbert / Vuorinen, Tapani / Argyropoulos, Dimitris S. / Balakshin, Yu / Barnett, J. R. / Burgert, Ingo / Rio, Jose C. / Evans, Robert / Evtuguin, Dmitry V. / Frazier, Charles E. / Fukushima, Kazuhiko / Gindl-Altmutter, Wolfgang / Glasser, W. G. / Holmbom, Bjarne / Isogai, Akira / Kadla, John F. / Koch, Gerald / Lachenal, Dominique / Laine, Christiane / Mansfield, Shawn D. / Morrell, J.J. / Niemz, Peter / Potthast, Antje / Ragauskas, Arthur J. / Ralph, John / Rice, Robert W. / Salin, Jarl-Gunnar / Schmitt, Uwe / Schultz, Tor P. / Sipilä, Jussi / Takano, Toshiyuki / Tamminen, Tarja / Theliander, Hans / Welling, Johannes / Willför, Stefan / Yoshihara, Hiroshi
12 Issues per year
IMPACT FACTOR 2016: 1.868
5-year IMPACT FACTOR: 1.875
CiteScore 2016: 1.83
SCImago Journal Rank (SJR) 2015: 0.817
Source Normalized Impact per Paper (SNIP) 2015: 0.954
Synthesis of glucose esters from cellulose in ionic liquids
The transformation of cellulose into glucose ester α-d-glucose pentaacetate (GPAc) was carried out in ionic liquid 1-butyl-3-methylimidazolium chloride under mild reaction conditions. The reaction comprises two steps: the first involves a hydrolysis reaction, yielding α-d-glucose and glucose oligomers; and then only after some time, the acetylating reagent acetic anhydride is added. Under optimized conditions and with the acidic resin Amberlyst 15DRY as a hydrolysis catalyst, a 70% yield of GPAc was obtained. This product could be quantitatively isolated by simple liquid-liquid extraction, which allowed easy recycling of the ionic liquid and catalyst.
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