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ent-Eudesmane sesquiterpenoids, galloyl esters of the oak lactone precursor, and a 3-O-methylellagic acid glycoside from the wood of Platycarya strobilacea.

Authors :
Maeda, Hajime
Kakoki, Narumi
Ayabe, Mami
Koga, Yuki
Oribe, Tomoko
Matsuo, Yosuke
Tanaka, Takashi
Kouno, Isao
Maeda, Hajime
Kakoki, Narumi
Ayabe, Mami
Koga, Yuki
Oribe, Tomoko
Matsuo, Yosuke
Tanaka, Takashi
Kouno, Isao
Publication Year :
2020

Abstract

ent-Eudesmane sesquiterpenoids, 8,11-dihydroxy-2,4-cycloeudesmane, 11-hydroxy-2,4-cycloeudesman-8-one and 2,4-cyclo-7(11)-eudesmen-8-one, were isolated from the wood of Platycarya strobilacea, which has been used as an aromatic tree since at least the 18th century. On charring the wood, 2,4-cyclo-7(11)-eudesmen-8-one was detected in the smoke. In the charred wood, the concentrations of ellagitannins, such as galloyl pedunculagin, dramatically decreased, whereas concentrations of pentagalloyl glucose, and other gallotannins were relatively stable. In addition, two other compounds, the 6'-O-m- and p-digalloyl oak lactone precursor and the 3-O-methylellagic acid 4'-O-(4″-O-galloyl)-xylopyranoside, were isolated from the charred wood along with m- and p-digallic acid.<br />identifier:Phytochemistry, 72(8), pp.796-803; 2011

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1375205518
Document Type :
Electronic Resource