1. The key glutarimides were obtained via facile [3+3] annulation. The method featured regioselective introduction of C-6 substituents in glutarimides, and application to the synthesis of natural products and pharmaceuticals.
2. The synthesis of a novel substituted aza-ticyclic compounds through the use of the intramolecular Diels-Alder reaction is present. Further aromaticzation in the present of BF3 to afford 2,3-dihydro-isoindolone.The use of method for the rapid preparation of a substituted isoindolone framework is described.
| Identifer | oai:union.ndltd.org:NSYSU/oai:NSYSU:etd-1007104-153717 |
| Date | 07 October 2004 |
| Creators | Chen, Bo-Fong |
| Contributors | Mou-Yung Yeh, Nein-Chen Chang, Cherng-Chyi Tzeng, Teng-Yuan Dong, Chin-Hsing Chou, Ming-Jung Wu |
| 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-1007104-153717 |
| Rights | off_campus_withheld, Copyright information available at source archive |
Page generated in 0.0018 seconds