Modified Synthesis of Isosalutaridine (Studies on the Syntheses of Heterocyclic Compounds. CCCXXXVI)
スポンサーリンク
概要
- 論文の詳細を見る
Diazotization of 1-(2-amino-5-benzyloxy-4-methoxybenzyl)-1,2,3,4-tetrahydro-6,7-dimethoxy-2-methylisoquinoline (V), followed by thermal decomposition without metallic catalyst, afforded the O-benzylisosalutaridine (VIII) in 10% yield, which was debenzylated to give isosalutaridine (IV).
- 社団法人日本薬学会の論文
- 1969-11-25
著者
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亀谷 哲治
Pharmaceutical Institute, Tohoku University School of Medicine
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福本 圭一郎
東北大・薬
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福本 圭一郎
Pharmaceutical Institute, Tohoku University
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亀谷 哲治
Pharmaceutical Institute Medical Faculty University Of Osaka
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福本 圭一郎
Pharmaceutical Institute Tohoku University School Of Medicine
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小泉 益男
Pharmaceutical Institute Tohoku University
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