ExLibris header image
SFX Logo
Title: Absolute Stereostructures of Three New Sesquiterpenes from the Fruit ofAlpiniaoxyphyllawith Inhibitory Effects on Nitric Oxide Production and Degranulation in RBL-2H3 Cells1
Source:

Journal of Natural Products [0163-3864] Morikawa, Toshio yr:2002


Collapse list of basic services Basic
Full text
Full text available via American Chemical Society Journals
GO
Document delivery
Request document via Library/Bibliothek GO
Users interested in this article also expressed an interest in the following:
1. Xu, J. "Inhibitory activity of eudesmane sesquiterpenes from Alpinia oxyphylla on production of nitric oxide." Bioorganic and medicinal chemistry letters 22.4 (2012): 1660-1663. Link to SFX for this item
2. Hikino, H. "Stereoselectivity in microbiological transformation of stereoisomers of .ALPHA.- cyperone and dihydro-.ALPHA.-cyperone with Colletotrichum phomoides." chemical & pharmaceutical bulletin 23.6 (1975): 1231-1240. Link to SFX for this item
3. Jiang, B. "New eudesmane sesquiterpenes from Alpinia oxyphylla and determination of their inhibitory effects on microglia." Bioorganic and medicinal chemistry letters 23.13 (2013): 3879-3883. Link to SFX for this item
4. Kutney, James P. "The chemistry of thujone. V. Thujone as a chiral synthon for the preparation of sesquiterpenes. Synthesis of (+)-carissone." Canadian journal of chemistry 60.14 (1982): 1842-1846. Link to SFX for this item
5. Cheng, S. "Three new eudesmanoids from the Formosan soft coralNephthea erecta." Journal of Asian natural products research 11.11 (2009): 967-973. Link to SFX for this item
Select All Clear All

Expand list of advanced services Advanced
A service provided by the Library of the Wissenschaftspark Albert Einstein, Potsdam, Germany.
© 2005 SFX by Ex Libris Inc.