| 標題: | Synthesis of tacamonine |
| 作者: | Ho, TL Gorobets, E 應用化學系 Department of Applied Chemistry |
| 關鍵字: | tacamonine;mannich reaction;Beckmann fragmentation |
| 公開日期: | 10-六月-2002 |
| 摘要: | 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. |
| URI: | http://dx.doi.org/10.1016/S0040-4020(02)00395-2 http://hdl.handle.net/11536/28723 |
| ISSN: | 0040-4020 |
| DOI: | 10.1016/S0040-4020(02)00395-2 |
| 期刊: | TETRAHEDRON |
| Volume: | 58 |
| Issue: | 24 |
| 起始頁: | 4969 |
| 結束頁: | 4973 |
| 顯示於類別: | 期刊論文 |

