Studies on Morphine Derivatives. II. The Stereochemistry of the By-products in the Synthesis of 3-Methoxy-N-methylmorphinan
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概要
- 論文の詳細を見る
The absolute configuration of (+)-10-hydroxy-1,2,3,3a, 11b, 11c-hexahydroaporphine A and B (IVa and IVb), which were obtained as by-products on the cyclization of (+)-1-(4-methoxybenzyl)-2-methyl-1,2,3,4,5,6,7,8-octahydroisoquinoline (I) to (+)-3-hydroxy-N-methylmorphinan (II) was established by degradation reaction to 3-alkyl cyclohexane-1,2-dicarboxylic acids.
- 公益社団法人日本薬学会の論文
- 1969-06-25
著者
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川崎 和彦
Shionogi Research Laboratory Shionogi & Co. Ltd.
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松村 宏
Shionogi Research Laboratory, Shionogi & Co., Ltd.
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松村 宏
Shionogi Research Laboratory Shionogi & Co. Ltd.