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1. A Versatile Approach to 6-Substituted-5-methoxy-d-lactam Framework and Application to the Synthesis of Natural Products and Pharmaceuticals 2. A New Approach to Isoindolone Skeleton

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.

Identiferoai:union.ndltd.org:NSYSU/oai:NSYSU:etd-1007104-153717
Date07 October 2004
CreatorsChen, Bo-Fong
ContributorsMou-Yung Yeh, Nein-Chen Chang, Cherng-Chyi Tzeng, Teng-Yuan Dong, Chin-Hsing Chou, Ming-Jung Wu
PublisherNSYSU
Source SetsNSYSU Electronic Thesis and Dissertation Archive
LanguageCholon
Detected LanguageEnglish
Typetext
Formatapplication/pdf
Sourcehttp://etd.lib.nsysu.edu.tw/ETD-db/ETD-search/view_etd?URN=etd-1007104-153717
Rightsoff_campus_withheld, Copyright information available at source archive

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