Studies on Optically Active Amino Acids. II. Partially Asymmetric Synthesis of 3-(3,4-Methylenedioxyphenyl) alanine.
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概要
- 論文の詳細を見る
Asymmetric hydrogenation of l-menthyl α-acetamido-3,4-methylenedioxycinnamate was carried out by two methods : i) 10% palladium-carbon in ethanol, ii) 10% palladium-carbon in benzene. Hydrogenation products were separated by fractional crystallization, and were converted to optically active 3-(3,4-methylenedioxyphenyl) alanines by transesterification followed by acid hydrolysis.
- 公益社団法人日本薬学会の論文
- 1962-08-25
著者
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塩入 孝之
Faculty of Pharmaceutical Sciences, Nagoya City University
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藤井 澄三
Faculty Of Pharmaceutical Sciences Kanazawa University
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山田 俊一
Faculty Of Pharmaceutical Sciences University Of Tokyo
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塩入 孝之
Faculty Of Pharmaceutical Sciences Nagoya City University
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