New Synthetic Approach to 3H-Carbacephems : Synthetic Studies on 1-Carbacephem Antibiotics
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概要
- 論文の詳細を見る
A new synthetic route to 3-H (3-unsubstituted) carbacephems was developed starting from readily available dialkyl aminomalonate and using intra-molecular aldol condensation for the construction of the 4,6-fused ring system.
- 社団法人日本薬学会の論文
- 1988-09-25
著者
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平田 正
Tokyo Research Laboratories Kyowa Hakko Kogyo Co. Ltd.
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持田 顕一
Kyowa Hakko Kogyo Co., Ltd., Tokyo Research Laboratories
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持田 顕一
Tokyo Research Laboratories, Kyowa Hakko Kogyo Co., Ltd.,
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持田 顕一
Kyowa Hakko Kogyo Co. Ltd. Tokyo Research Laboratories
関連論文
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- Studies on Cardiotonic Agents. III. : Synthesis of 1-[1-(6,7-Dimethoxy-4-quinazolinyl)-4-piperidinyl]-3-substituted 2-Imidazolidinone and 2-Imidazolidinethione Derivatives
- Studies on Cardiotonic Agents. I. : Synthesis of Some Quinazoline Derivatives
- Synthesis and Biological Evaluation of Quinocarcin Derivatives
- Synthesis of 1,2-Disubstituted-1-carbacephem
- Synthesis and Biological Evaluation of 3-Chloro-1-carbacephem Compounds
- Synthesis and Biological Evaluation of Optically Active 3-H-1-Carbacephem Compounds
- Synthetic Studies on 1,2-Dehydro-1-carbacephem Compounds
- New Synthetic Approach to 3H-Carbacephems : Synthetic Studies on 1-Carbacephem Antibiotics
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