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A New Approach to Benzo[h]quinoline Skeleton

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.

Identiferoai:union.ndltd.org:NSYSU/oai:NSYSU:etd-0725107-214140
Date25 July 2007
CreatorsHuang, Chiao-wei
ContributorsChin-Hsing Chou, Nien-Chen Chang, Cherng-Chyi Tzeng, Tai, H.-M.
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-0725107-214140
Rightsunrestricted, Copyright information available at source archive

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