Synthesis of tangutorine

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DC Field	Value	Language
dc.contributor.author	Ho, TL	en_US
dc.contributor.author	Chen, CK	en_US
dc.date.accessioned	2014-12-08T15:17:35Z	-
dc.date.available	2014-12-08T15:17:35Z	-
dc.date.issued	2006	en_US
dc.identifier.issn	0018-019X	en_US
dc.identifier.uri	http://hdl.handle.net/11536/12762	-
dc.identifier.uri	http://dx.doi.org/10.1002/hlca.200690003	en_US
dc.description.abstract	Tangutorine (1) in the racemic form has been assembled from tryptamine and aldehyde 3. The synthetic design was based on uncovering a hidden symmetry in the nontryptamine portion of the norketone 2. A five-step process with an overall yield of 7% was developed in which 2 was transformed into the target molecule via a Vilsineier-Haack reaction and two reduction steps.	en_US
dc.language.iso	en_US	en_US
dc.title	Synthesis of tangutorine	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1002/hlca.200690003	en_US
dc.identifier.journal	HELVETICA CHIMICA ACTA	en_US
dc.citation.volume	89	en_US
dc.citation.issue	1	en_US
dc.citation.spage	122	en_US
dc.citation.epage	126	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:000234988100013	-
dc.citation.woscount	12	-
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