Synthesis of tacamonine

完整後設資料紀錄

DC 欄位	值	語言
dc.contributor.author	Ho, TL	en_US
dc.contributor.author	Gorobets, E	en_US
dc.date.accessioned	2014-12-08T15:42:18Z	-
dc.date.available	2014-12-08T15:42:18Z	-
dc.date.issued	2002-06-10	en_US
dc.identifier.issn	0040-4020	en_US
dc.identifier.uri	http://dx.doi.org/10.1016/S0040-4020(02)00395-2	en_US
dc.identifier.uri	http://hdl.handle.net/11536/28723	-
dc.description.abstract	Tacamonine has been synthesized in 3.2% overall yield from cyclohexanone-4-carboxylic acid ethyleneacetal. The tetrahydro-beta-carboline intermediate was submitted to a Mannich reaction to provide a bridged ring system embodying latent branches of the quinolizidine portion. The final stages included fragmentation and Grignard reaction. (C) 2002 Published by Elsevier Science Ltd.	en_US
dc.language.iso	en_US	en_US
dc.subject	tacamonine	en_US
dc.subject	mannich reaction	en_US
dc.subject	Beckmann fragmentation	en_US
dc.title	Synthesis of tacamonine	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1016/S0040-4020(02)00395-2	en_US
dc.identifier.journal	TETRAHEDRON	en_US
dc.citation.volume	58	en_US
dc.citation.issue	24	en_US
dc.citation.spage	4969	en_US
dc.citation.epage	4973	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:000176179800027	-
dc.citation.woscount	14	-
顯示於類別：	期刊論文

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