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Hydrothermolysis of Flavonoids in Relation to Steaming of Japanese Larch Wood

  • W. Ohmura , S. Ohara , K. Hashida , M. Aoyama and S. Doi
Published/Copyright: June 1, 2005
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Holzforschung
From the journal Volume 56 Issue 5

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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