Volume 94, Issue 3 pp. 474-480
Research Article

New Eremophilenolides from Senecio dianthus

Yan-Hui Li

Yan-Hui Li

College of Horticulture, Shenyang Agricultural University, Shenyang 110161, P. R. China, (phone: +86-24-88487144)

Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, P. R. China, (phone: +86-28-85239109)

Search for more papers by this author
Yan Zhou

Yan Zhou

Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, P. R. China, (phone: +86-28-85239109)

Search for more papers by this author
Gesang Suolang

Gesang Suolang

Tibet Autonomous Region Institute for Food and Drug Control, Lhasa 850000, P. R. China

Search for more papers by this author
Ciren Bianba

Ciren Bianba

Tibet Autonomous Region Institute for Food and Drug Control, Lhasa 850000, P. R. China

Search for more papers by this author
Li-Sheng Ding

Corresponding Author

Li-Sheng Ding

Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, P. R. China, (phone: +86-28-85239109)

Li-Sheng Ding, Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, P. R. China, (phone: +86-28-85239109)

Hui Feng, College of Horticulture, Shenyang Agricultural University, Shenyang 110161, P. R. China, (phone: +86-24-88487144)

Search for more papers by this author
Hui Feng

Corresponding Author

Hui Feng

College of Horticulture, Shenyang Agricultural University, Shenyang 110161, P. R. China, (phone: +86-24-88487144)

Li-Sheng Ding, Chengdu Institute of Biology, Chinese Academy of Sciences, Chengdu 610041, P. R. China, (phone: +86-28-85239109)

Hui Feng, College of Horticulture, Shenyang Agricultural University, Shenyang 110161, P. R. China, (phone: +86-24-88487144)

Search for more papers by this author
First published: 14 March 2011
Citations: 5

Abstract

From the aerial parts of Senecio dianthus, four new eremophilenolides (14, resp.) and one new eremophilenolide alkaloid (5), of the relatively uncommon eremophilenoid-type sesquiterpenoid lactones, were isolated together with three known sesquiterpenoid lactones, 10β-hydroxyeremophil-7(11)-en-12,8α-olide (6), 8β,10β-dihydroxyeremophil-7(11)-en-12,8α-olide (7), and 10α-hydroxy-1-oxoeremophila-7(11),8(9)-dien-12,8-olide (8). On the basis of IR, MS, and NMR data, particularly 2D-NMR analyses, the structures of the new compounds were established as: 2β-(angeloyloxy)-10β-hydroxyeremophil-7(11)-en-12,8α-olide (1), 6β-(angeloyloxy)-10β-hydroxyeremophil-7(11)-en-12,8α-olide (2), 2β-(angeloyloxy)-8β,10β-dihydroxyeremophil-7(11)-en-12,8α-olide (3), 2β-(angeloyloxy)-8α-hydroxyeremophila-7(11),9(10)-dien-12,8β-olide (4), and 8β-amino-10β-hydroxyeremophil-7(11)-en-12,8α-olide (5). In addition, the relative configuration of 1 was corroborated by X-ray diffraction analysis.

The full text of this article hosted at iucr.org is unavailable due to technical difficulties.