Stereochemical Studies. LI. Stereochemical Courses of Deaminative Bromination of L-Aspartic Acid and Its Esters
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概要
- 論文の詳細を見る
Stereochemical studies on the deaminative bromination of L-aspartic acid (1a) and its esters (1b, 1c, and 1d) have shown that α-carboxyl group almost completely holds the configuration in this substitution reaction, while β-carboxyl group has no ability to exhibit such neighboring group participation.
- 公益社団法人日本薬学会の論文
- 1978-01-25
著者
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村上 泰興
Faculty of Pharmaceutical Sciences, University of Tokyo
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村上 泰興
東邦大学薬学部
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Koga Kenjiro
Department Of Pharmaceutics Faculty Of Pharmaceutical Sciences Hokuriku University
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- Stereochemical Studies. LI. Stereochemical Courses of Deaminative Bromination of L-Aspartic Acid and Its Esters