Stereoselective Reactions. IX. Synthetic Studies on Optically Active β-Lactams. I. Chiral Synthesis of Carbapenam and Carbapenem Ring Systems Starting from (S)-Aspartic Acid
スポンサーリンク
概要
- 論文の詳細を見る
A chiral carbapenam ring system ((3R, 5R)-(+)-19 and -20) having the desired absolute configuration at C-5 was synthesized starting from (S)-aspartic acid, and the latter product was further transformed to a chiral carbapenem derivative ((5S, 2'R)-(+)-21) having an (R)-cysteine moiety as a side chain.
- 公益社団法人日本薬学会の論文
- 1985-08-25
著者
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古賀 憲司
Faculty of Pharmaceutical Sciences, University of Tokyo
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Koga Kenjiro
Department Of Pharmaceutics Faculty Of Pharmaceutical Sciences Hokuriku University
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伊古田 暢夫
Faculty of Pharmaceutical Sciences, University of Tokyo
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柴田 久就
Faculty Of Pharmaceutical Sciences University Of Tokyo
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伊古田 暢夫
National Institute Of Radiological Sciences
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