Synthesis of cryptolepine and cryptoteckieine from a common intermediate

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DC Field	Value	Language
dc.contributor.author	Ho, TL	en_US
dc.contributor.author	Jou, DG	en_US
dc.date.accessioned	2014-12-08T15:42:54Z	-
dc.date.available	2014-12-08T15:42:54Z	-
dc.date.issued	2002	en_US
dc.identifier.issn	0018-019X	en_US
dc.identifier.uri	http://hdl.handle.net/11536/29077	-
dc.identifier.uri	http://dx.doi.org/10.1002/1522-2675(200211)85:11<3823	en_US
dc.description.abstract	Both cryptolepine 1 and cryptotackieine 3 have been synthesized from 1,3-bis(2-nitrophenyl)propan-2-one. The approach to 1 involved reduction of the NO2 groups, oxidative cyclization with Phl(OAc)(2), and N-methylation, whereas 3 was obtained via bromination, Favorskii rearrangement, reduction (in situ cyclization), and N-methylation.	en_US
dc.language.iso	en_US	en_US
dc.title	Synthesis of cryptolepine and cryptoteckieine from a common intermediate	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1002/1522-2675(200211)85:11<3823	en_US
dc.identifier.journal	HELVETICA CHIMICA ACTA	en_US
dc.citation.volume	85	en_US
dc.citation.issue	11	en_US
dc.citation.spage	3823	en_US
dc.citation.epage	3827	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:000179932000016	-
dc.citation.woscount	35	-
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