Jie-qing Liu

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Name:
Organization: Kunming Institute of Botany
Department: State Key Laboratory of Photochemistry and Plant Resources in West China
Title:
Co-reporter:Xu-Yang Li, Yuan-Feng Yang, Xing-Rong Peng, Ming-Ming Li, Liang-Qun Li, Xu Deng, Hong-Bo Qin, Jie-Qing Liu, and Ming-Hua Qiu
Organic Letters 2014 Volume 16(Issue 8) pp:2196-2199
Publication Date(Web):April 3, 2014
DOI:10.1021/ol500692j
High contents of curcusones A and B and trace amounts of spirocurcasone exist in the roots of Jatropha curcas. Here, a one-step semisynthesis method of spirocurcasone and pyracurcasone was built, not only resulted an increased yield of spirocurcasone but also produced pyracurcasone, which exhibited greater cytotoxicity compared to curcusones A and B. The plausible mechanism of the formation of pyracurcasone was proposed, and the proposed biogenetic origin for spirocurcasone by Taglialatela-Scafati was confirmed.
Nic-2
Nic 11
(S)-6-((S,E)-6-(5,5-dimethyl-4-oxo-4,5-dihydrofuran-2-yl)-6-hydroxy-2-methylhept-1-en-1-yl)-4-methyl-5,6-dihydro-2H-pyran-2-one
1-O-deacetyl-2alpha-methoxylkhayanolide E
(5R,9R,10R,13S,14S,17S)-17-{(1R)-1-[3-(1,2-dihydroxy-2-methylpropyl)oxiran-2-yl]ethyl}-1,2,4,5,6,9,10,11,12,13,14,15,16,17-tetradecahydro-4,4,10,13,14-pentamethyl-3H-cyclopenta[a]phenanthren-3-one
(3beta,23R)-cucurbita-5,24-dien-7-one-3,23-diol
kuguacin P
kuguacin L
3beta-hydroxy-7beta-methoxycucurbita-5,24-dien-23-yl beta-glucopyranoside