Chemical studies on nitrogen heterocyclic skeleton of the Daphniphyllum alkaloids |
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Authors: | H. Niwa M. Toda S. Ishimaru Y. Hirata S. Yamamura |
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Affiliation: | Chemical Institute, Nagoya University, Chikusa-ku, Nagoya Japan;Faculty of Pharmacy, Meijo University, Showa-ku, Nagoya, Japan |
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Abstract: | From a biogenetic point of view, a great variety of related alkaloids isolated from the plant Daphniphyllaceae are related to one another by bond formation or fission. Thus, daphnialcohol acetate (6), a derivative of the degradation products of daphniphylline (1), was subjected to von Braun degradation followed by acid-catalyzed recyclization to give an isomer (8) of daphnialcohol, which has a new type of nitrogen heterocyclic skeleton. Furthermore, daphnilactone-B (3) was converted into a daphniphylline-type compound (19) via a plausible intermediate (21). |
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