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dc.contributor.authorHo, TLen_US
dc.contributor.authorChein, RJen_US
dc.date.accessioned2014-12-08T15:39:44Z-
dc.date.available2014-12-08T15:39:44Z-
dc.date.issued2004-01-23en_US
dc.identifier.issn0022-3263en_US
dc.identifier.urihttp://dx.doi.org/10.1021/jo035561yen_US
dc.identifier.urihttp://hdl.handle.net/11536/27127-
dc.description.abstractThe 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.isoen_USen_US
dc.titleIntervention of phenonium ion in Ritter reactionsen_US
dc.typeArticleen_US
dc.identifier.doi10.1021/jo035561yen_US
dc.identifier.journalJOURNAL OF ORGANIC CHEMISTRYen_US
dc.citation.volume69en_US
dc.citation.issue2en_US
dc.citation.spage591en_US
dc.citation.epage592en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000188496300050-
dc.citation.woscount6-
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