Studies on Optically Active Amino Acids. III. Preparation of 3-(3, 4-Dihydroxyphenyl)-DL-, -D-, and -L-alanine
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Hydrolyses of the racemate and the optical isomers of 3, 4-methylenedioxyphenylalanine (I), and of their N-acetyl derivatives (DL-, D-, and L-(II)) including the l-menthyl esters (IIIa and IIIb) were smoothly effected by using a mixture of HI, Ac2O and red phosphorus to furnish the corresponding racemate and optical isomers of 3-(3, 4-dihydroxyphenyl) alanine (Dopa) in fair yields.<BR>This method would be a new and advantageous way for the preparation of DL-, D-, and L-Dopa, when combined with the previously reported preparation of the racemic and optically active intermediates. The absolute configurations of the optical isomers of (I), of their N-acetyl derivatives (D- and L-(I)), and of the l-menthyl esters (IIIa and IIIb) were simultaneously established by the above hydrolyses.
収録刊行物
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- CHEMICAL & PHARMACEUTICAL BULLETIN
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CHEMICAL & PHARMACEUTICAL BULLETIN 10 (8), 693-697, 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
- 1390001204172169088
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- NII論文ID
- 110003618932
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- NII書誌ID
- AA00602100
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- ISSN
- 13475223
- 00092363
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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
- CiNii Articles
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- 抄録ライセンスフラグ
- 使用不可