Intervention of phenonium ion in Ritter reactions

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DC Field	Value	Language
dc.contributor.author	Ho, TL	en_US
dc.contributor.author	Chein, RJ	en_US
dc.date.accessioned	2014-12-08T15:39:44Z	-
dc.date.available	2014-12-08T15:39:44Z	-
dc.date.issued	2004-01-23	en_US
dc.identifier.issn	0022-3263	en_US
dc.identifier.uri	http://dx.doi.org/10.1021/jo035561y	en_US
dc.identifier.uri	http://hdl.handle.net/11536/27127	-
dc.description.abstract	The transformation of phenylethyl chloride to 3,4-dihydroisoquinolines is shown to proceed via phenonium ion. The evidence comes from a study of dideuterated analogue 4, and the monomethylated and dimethylated compounds 2 and 3.	en_US
dc.language.iso	en_US	en_US
dc.title	Intervention of phenonium ion in Ritter reactions	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1021/jo035561y	en_US
dc.identifier.journal	JOURNAL OF ORGANIC CHEMISTRY	en_US
dc.citation.volume	69	en_US
dc.citation.issue	2	en_US
dc.citation.spage	591	en_US
dc.citation.epage	592	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:000188496300050	-
dc.citation.woscount	6	-
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