Synthesis of tangutorine
| dc.citation.epage | 126 | en_US |
| dc.citation.issue | 1 | en_US |
| dc.citation.spage | 122 | en_US |
| dc.citation.volume | 89 | en_US |
| dc.citation.woscount | 12 | |
| dc.contributor.author | Ho, TL | en_US |
| dc.contributor.author | Chen, CK | en_US |
| dc.contributor.department | 應用化學系 | zh_TW |
| dc.contributor.department | Department of Applied Chemistry | en_US |
| dc.date.accessioned | 2014-12-08T15:17:35Z | |
| dc.date.available | 2014-12-08T15:17:35Z | |
| dc.date.issued | 2006 | en_US |
| dc.description.abstract | Tangutorine (1) in the racemic form has been assembled from tryptamine and aldehyde 3. The synthetic design was based on uncovering a hidden symmetry in the nontryptamine portion of the norketone 2. A five-step process with an overall yield of 7% was developed in which 2 was transformed into the target molecule via a Vilsineier-Haack reaction and two reduction steps. | en_US |
| dc.identifier.doi | 10.1002/hlca.200690003 | en_US |
| dc.identifier.issn | 0018-019X | en_US |
| dc.identifier.journal | HELVETICA CHIMICA ACTA | en_US |
| dc.identifier.uri | http://dx.doi.org/10.1002/hlca.200690003 | en_US |
| dc.identifier.uri | https://ir.lib.nycu.edu.tw/handle/11536/12762 | |
| dc.identifier.wosnumber | WOS:000234988100013 | |
| dc.language.iso | en_US | en_US |
| dc.title | Synthesis of tangutorine | en_US |
| dc.type | Article | en_US |