Synthetic Studies on 1,2-Dehydro-1-carbacephem Compounds
スポンサーリンク
概要
- 論文の詳細を見る
7-Azido-1,2-dehydro-1-carbacephem 13 was efficiently synthesized by employing ketene-imine cycloaddition, intramolecular Horner-Emmons reaction and elimination of a phenylsulfoxide group or an ammonium group. 7-Acylamino 1,2-dehydro-1-carbacephems, 18 and 19,were obtained from 13. Infrared absorption frequencies of the β-lactam carbonyl in 1,2-dehydro-1-carbacephem compounds thus prepared are equal to or higher than those of the corresponding 1-carbacephem compounds. However, 18 and 19 exhibited very poor antibacterial activity.
- 社団法人日本薬学会の論文
- 1989-02-25
著者
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平田 正
Tokyo Research Laboratories Kyowa Hakko Kogyo Co. Ltd.
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斉藤 博満
Kyowa Hakko Kogyo Co., Ltd., Tokyo Research Laboratories
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平田 正
Kyowa Hakko Kogyo Co., Ltd., Tokyo Research Laboratories
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松島 日出夫
Kyowa Hakko Kogyo Co., Ltd., Tokyo Research Laboratories
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白木 千尋
Kyowa Hakko Kogyo Co., Ltd., Tokyo Research Laboratories
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斉藤 博満
Kyowa Hakko Kogyo Co. Ltd. Tokyo Research Laboratories
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松島 日出夫
Kyowa Hakko Kogyo Co. Ltd. Tokyo Research Laboratories
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白木 千尋
Kyowa Hakko Kogyo Co. Ltd. Tokyo Research Laboratories
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