Intervention of phenonium ion in Ritter reactions
| dc.citation.epage | 592 | en_US |
| dc.citation.issue | 2 | en_US |
| dc.citation.spage | 591 | en_US |
| dc.citation.volume | 69 | en_US |
| dc.citation.woscount | 6 | |
| dc.contributor.author | Ho, TL | en_US |
| dc.contributor.author | Chein, RJ | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | 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.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.identifier.doi | 10.1021/jo035561y | en_US |
| dc.identifier.issn | 0022-3263 | en_US |
| dc.identifier.journal | JOURNAL OF ORGANIC CHEMISTRY | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1021/jo035561y | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/27127 | |
| dc.identifier.wosnumber | WOS:000188496300050 | |
| dc.language.iso | en_US | en_US |
| dc.title | Intervention of phenonium ion in Ritter reactions | en_US |
| dc.type | Article | en_US |