Synthesis of tacamonine
| dc.citation.epage | 4973 | en_US |
| dc.citation.issue | 24 | en_US |
| dc.citation.spage | 4969 | en_US |
| dc.citation.volume | 58 | en_US |
| dc.citation.woscount | 14 | |
| dc.contributor.author | Ho, TL | en_US |
| dc.contributor.author | Gorobets, E | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:42:18Z | |
| dc.date.available | 2014-12-08T15:42:18Z | |
| dc.date.issued | 2002-06-10 | en_US |
| 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.identifier.doi | 10.1016/S0040-4020(02)00395-2 | en_US |
| dc.identifier.issn | 0040-4020 | en_US |
| dc.identifier.journal | TETRAHEDRON | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1016/S0040-4020(02)00395-2 | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/28723 | |
| dc.identifier.wosnumber | WOS:000176179800027 | |
| 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 |