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Hydrothermolysis of Flavonoids in Relation to Steaming of Japanese Larch Wood
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W. Ohmura
Published/Copyright:
June 1, 2005
Summary
Four flavonoid compounds, ((+)-taxifolin, (+)-aromadendrin, quercetin and (−)-naringenin), from Japanese larch (Larix leptolepis) wood were heated at 170 ℃C for 60 min at pH=3.46 (hydrothermolysis treatment). Alphitonin, four taxifolin steric isomers and quercetin were recovered from the treatment of (+)-taxifolin, and maesopsin, four aromadendrin steric isomers and kaempferol from (+)-aromadendrin. The reaction products from (−)-naringenin were found to be a mixture with (+)-naringenin. Quercetin was not changed by the treatment. Possible pathways for the formation of these products are discussed.
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Published Online: 2005-06-01
Published in Print: 2002-08-26
Copyright © 2002 by Walter de Gruyter GmbH & Co. KG
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Articles in the same Issue
- Effect of Growth Rate on Fibre Characteristics in Norway Spruce (Picea abies (L.) Karst.)
- Techniques for Measuring Growth Stress on the Xylem Surface Using Strain and Dial Gauges
- Use of Soft Rot Cavities to Determine Microfibril Angles in Wood; Advantages, Disadvantages and Possibilities
- Surface Roughness and Color Change of Copper-Amine Treated Red Maple (Acer rubrum) Exposed to Artificial Ultraviolet Light
- Differences in Resin Acid Concentration between Brown-Rot Resistant and Susceptible Scots Pine Heartwood
- Antioxidant Activity of Abietane-Type Diterpenes from Heartwood of Taiwania cryptomerioides Hayata
- Hydrothermolysis of Flavonoids in Relation to Steaming of Japanese Larch Wood
- Impact of Pulping Conditions on FORMACELL Aspen Lignin: Investigation of Methoxyl and Ester Groups, Carbohydrates, Molar Mass and Glass Transition Temperatures
- Ethanol-Enhanced Alkaline Pulping of Arundo donax L. Reed: Influence of Solvent on Pulp Yield and Quality
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