Synthetic studies on (+)-naphthyridinomycin: stereoselective synthesis of the tetracyclic core framework |
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Authors: | Mori Kazuki Rikimaru Kentaro Kan Toshiyuki Fukuyama Tohru |
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Institution: | Graduate School of Pharmaceutical Sciences, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, Japan. |
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Abstract: | reaction: see text] The stereoselective synthesis of the tetracyclic intermediate 21 for (+)-naphthyridinomycin (1) has been accomplished. The convergent synthesis used the Ugi 4CC reaction with the amine derivative 10. The key features of the stereoselective synthesis of 21 were the intramolecular Mizoroki-Heck reaction, an aromatic-aldehyde cyclization, and a stereoselective hydroboration. |
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