Research output: Contribution to conference - Without ISBN/ISSN › Abstract › peer-review
Research output: Contribution to conference - Without ISBN/ISSN › Abstract › peer-review
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TY - CONF
T1 - Mechanistic studies on the dehydration of glucose to 5-hydroxymethylfurfural and xylose to furfural
AU - Akien, Geoffrey
AU - Qi, Long
AU - Horvath, Istvan T.
PY - 2013/4/10
Y1 - 2013/4/10
N2 - Glucose, the monomer of cellulose, co-monomer of hemi-cellulose, and one of the components of sucrose, is one of the most important monosaccharides in the acid-catalyzed valorization of carbohydrates. Several pathways have been proposed for its conversion to 5-hydroxymethyl-furfural involving the isomerization of glucose to fructose, the transient formation of 3-deoxy-ᴅ-erythro-hexos-2-ulose or levoglucosenone, and the dehydration at the C-2 position followed by a ring contraction. Isotope labeling experiments have been used to establish the mechanism under specific reaction conditions. Similar mechanisms are operating for the conversion of xylose to furfural.
AB - Glucose, the monomer of cellulose, co-monomer of hemi-cellulose, and one of the components of sucrose, is one of the most important monosaccharides in the acid-catalyzed valorization of carbohydrates. Several pathways have been proposed for its conversion to 5-hydroxymethyl-furfural involving the isomerization of glucose to fructose, the transient formation of 3-deoxy-ᴅ-erythro-hexos-2-ulose or levoglucosenone, and the dehydration at the C-2 position followed by a ring contraction. Isotope labeling experiments have been used to establish the mechanism under specific reaction conditions. Similar mechanisms are operating for the conversion of xylose to furfural.
M3 - Abstract
T2 - 245th ACS National Meeting
Y2 - 7 April 2013 through 12 April 2013
ER -