We use stepwise [3+3] annulation to prepare the asymmetric glutarimides, and then we can build substituent group in C6 position after choosing regioselective addition reaction. And we establish a new approach to benzo[h]quinoline skeleton starting from glutarimides via ring-closing reaction. Finally, we applied this method to the synthetic studies toward benzo[h]quinoline derivatives.
| Identifer | oai:union.ndltd.org:NSYSU/oai:NSYSU:etd-0725107-214140 |
| Date | 25 July 2007 |
| Creators | Huang, Chiao-wei |
| Contributors | Chin-Hsing Chou, Nien-Chen Chang, Cherng-Chyi Tzeng, Tai, H.-M. |
| Publisher | NSYSU |
| Source Sets | NSYSU Electronic Thesis and Dissertation Archive |
| Language | Cholon |
| Detected Language | English |
| Type | text |
| Format | application/pdf |
| Source | http://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-0725107-214140 |
| Rights | unrestricted, Copyright information available at source archive |
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