Studies on Optically Active Amino Acids. II. Partially Asymmetric Synthesis of 3-(3, 4-Methylenedioxyphenyl) alanine
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抄録
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.
収録刊行物
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- CHEMICAL & PHARMACEUTICAL BULLETIN
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CHEMICAL & PHARMACEUTICAL BULLETIN 10 (8), 688-693, 1962
公益社団法人 日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1390001204172168064
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- NII論文ID
- 110003618931
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- NII書誌ID
- AA00602100
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- ISSN
- 13475223
- 00092363
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- PubMed
- 14002246
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- 本文言語コード
- en
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- データソース種別
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- JaLC
- Crossref
- PubMed
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可