Studies on Ergot Alkaloids and Related Compounds. XI. Synthesis of trans-and cis-4-Mehyl-1,2,3,4,4a, 5,6,10b-octahydrobenzo [f] quinoline
スポンサーリンク
概要
- 論文の詳細を見る
trans-4-Methyl-1,2,3,4,4a, 5,6,10b-octahydrobenzo [f] quinoline (III) was prepared by Birch reduction of 4-methyl-1,2,3,4,5,6-hexahydrobenzo [f] quinoline (I) and by Clemmensen reduction of trans-4-methyl-3,4,4a, 5,6,10b-hexahydrobenzo [f] quinolin-1(2H)-one (V). The cis isomer (II) of III was prepared by lithium aluminum hydride reduction of cis -4-methyl-1,2,4a, 5,6,10b-hexahydrobenzo [f] quinolin 3-(4H)-one (IV).
- 公益社団法人日本薬学会の論文
- 1964-12-25
著者
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田村 恭光
Faculty Of Pharmaceutical Sciences Osaka University
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岩田 宙造
Faculty of Pharmaceutical Sciences, Osaka University
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堀井 善一
Faculty Of Pharmaceutical Sciences Josai University
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岩田 宙造
Faculty Of Pharmaceutical Sciences Osaka University
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