ハロゲン置換N-Benzyl-β-phenethylamine誘導体の光化学反応について
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概要
- 論文の詳細を見る
Apogalanthamine analogs (1-4), were prepared by photolysis of the hydrochlorides of halogeno-N-benzyl-β-phenethylamine derivatives (5-8). The yield of 3 and 4 from the halogeno-amines (7,11 and 8,12,respectively) having a halogen atom in the benzyl group were found to be better than those of 1 and 2 from the halides (5,9 and 6,10,respectively) having a halogen atom in the phenethyl group. On photolysis, the analogs (1-4) seem to be formed via a phenyl radical (I or II) and a cyclohexadienyl radical (III or IV).
- 公益社団法人日本薬学会の論文
- 1978-07-25
著者
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小林 茂
Faculty Of Home Economics Shikoku University
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木原 勝
徳島大学薬学部
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木原 勝
Faculty Of Pharmaceutical Sciences The University Of Tokushima
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小林 茂
徳島大学薬学部
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松本 宏
徳島大学薬学部
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