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Isolation and Structure of Three Bislactones, Eremopetasitenin B4and Eremofarfugins F and G, fromLigularia przewalskiiand Revision of the Structure of an Epoxy-lactone Isolated fromLigularia intermedia
Author(s) -
Yoshinori Saito,
Aya Kamada,
Yasuko Okamoto,
Xun Gong,
Chiaki Kuroda,
Motoo Tori
Publication year - 2014
Publication title -
chemistry letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.492
H-Index - 114
eISSN - 1348-0715
pISSN - 0366-7022
DOI - 10.1246/cl.140745
Subject(s) - lactone , chemistry , sesquiterpene lactone , stereochemistry , diastereomer , asteraceae , enol , organic chemistry , botany , sesquiterpene , biology , catalysis
Three bislactones belonging to the eremophilane type were isolated from Ligularia przewalskii (Asteraceae): an epoxylactone (eremopetasitenin B4) identical to the previously isolated lactone, whose structure was revised in this work; a new enollactone (eremofarfugin F); and its diastereoisomer at C-11 (eremofarfugin G). This was identical to the reported lactone, whose stereochemistry was left undetermined. The stereochemistry along with the NMR data of this diastereoisomer was assigned in this study

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