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 |
Page generated in 0.0019 seconds