Synthesis of tavacpallescensin and occidol via a common intermediate

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DC Field	Value	Language
dc.contributor.author	Ho, TL	en_US
dc.contributor.author	Lin, YJ	en_US
dc.date.accessioned	2014-12-08T15:46:36Z	-
dc.date.available	2014-12-08T15:46:36Z	-
dc.date.issued	1999-05-07	en_US
dc.identifier.issn	0300-922X	en_US
dc.identifier.uri	http://dx.doi.org/10.1039/a900465c	en_US
dc.identifier.uri	http://hdl.handle.net/11536/31343	-
dc.description.abstract	The symmetrical benzosuberone 3 has been used in the synthesis of tavacpallescensin by an Emmons-Wadsworth condensation, selenium dioxide oxidation and diisobutylaluminium hydride reduction. For the elaboration of occidol, alpha-diazotization, Wolff rearrangement and reaction with methyllithium were involved.	en_US
dc.language.iso	en_US	en_US
dc.title	Synthesis of tavacpallescensin and occidol via a common intermediate	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1039/a900465c	en_US
dc.identifier.journal	JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1	en_US
dc.citation.volume		en_US
dc.citation.issue	9	en_US
dc.citation.spage	1207	en_US
dc.citation.epage	1210	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:000080386000019	-
dc.citation.woscount	13	-
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