A stereoselective synthesis of platyphyllide

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DC Field	Value	Language
dc.contributor.author	Ho, TL	en_US
dc.contributor.author	Ho, MF	en_US
dc.date.accessioned	2014-12-08T15:46:23Z	-
dc.date.available	2014-12-08T15:46:23Z	-
dc.date.issued	1999-07-07	en_US
dc.identifier.issn	0300-922X	en_US
dc.identifier.uri	http://dx.doi.org/10.1039/a902410g	en_US
dc.identifier.uri	http://hdl.handle.net/11536/31211	-
dc.description.abstract	The norsesquiterpene lactone, platyphyllide has been synthesized in 8 steps in 23% overall yield via the Diels-Alder adduct of 2-(4-methylpent-3-enyl)furan with dimethyl acetylenedicarboxylate, the 3-substituted phthalic diester, and an o-formylbenzamide. An intramolecular ene reaction established the skeleton, and the final step involved inversion of configuration at the benzylic site.	en_US
dc.language.iso	en_US	en_US
dc.title	A stereoselective synthesis of platyphyllide	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1039/a902410g	en_US
dc.identifier.journal	JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1	en_US
dc.citation.volume		en_US
dc.citation.issue	13	en_US
dc.citation.spage	1823	en_US
dc.citation.epage	1826	en_US
dc.contributor.department	應用化學系	zh_TW
dc.contributor.department	Department of Applied Chemistry	en_US
dc.identifier.wosnumber	WOS:000081549700007	-
dc.citation.woscount	10	-
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