Published November 30, 2014 | Version v1
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Fig. 6 in Arachidonic acid-dependent carbon-eight volatile synthesis from wounded liverwort (Marchantia polymorpha)

Description

Fig. 6. Resolution of enantiomers of 5 formed from racemic 3. The crude enzyme extract prepared from des6KO thalli was reacted with racemic 3, and the 5 formed by enzyme catalyzed hydrolysis was subjected to chiral phase GC analysis (upper chromatogram). 5 was not detected with the reaction mixture prepared without substrate (middle chromatogram) or without enzyme (lower chromatogram).

Notes

Published as part of Kihara, Hirotomo, Tanaka, Maya, Yamato, Katsuyuki T., Horibata, Akira, Yamada, Atsushi, Kita, Sayaka, Ishizaki, Kimitsune, Kajikawa, Masataka, Fukuzawa, Hideya, Kohchi, Takayuki, Akakabe, Yoshihiko & Matsui, Kenji, 2014, Arachidonic acid-dependent carbon-eight volatile synthesis from wounded liverwort (Marchantia polymorpha), pp. 42-49 in Phytochemistry 107 on page 45, DOI: 10.1016/j.phytochem.2014.08.008, http://zenodo.org/record/10491050

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Journal article: 10.1016/j.phytochem.2014.08.008 (DOI)
Journal article: urn:lsid:plazi.org:pub:FFE7FFEBB652FFE9FFC78E259B78FFAF (LSID)
Journal article: https://zenodo.org/record/10491050 (URL)