Elimination of the 4-hydroxyl group of the alkaloids related to morphine—I |
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Authors: | Y. K. Sawa N. Tsuji S. Maeda |
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Affiliation: | Research Laboratory, Shionogi & Co., Ltd. Osaka, Japan |
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Abstract: | Sinomenine, an alkaloid of the Japanese plant Sinomenium acutum, was converted to the 4-phenylether by the Ullmann reaction in a good yield. The Clemmensen reduction of sinomenine-phenylether and of its derivatives gave (+)-3-methoxy-4-phenoxy-N-methyl-Δx-morphinan. Hydrogenation and successive sodium-liquid ammonia reduction of (+)-3-methoxy-4-phenoxy-N-methyl-Δx-morphinan gave (+)-3-methoxy-N-methylmorphinan. |
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