The Improved Syntheses of dl-Ibotenic Acid and Muscimol
スポンサーリンク
概要
- 論文の詳細を見る
dl-Ibotenic acid (I) was synthesized in a better yield than the known methods, starting from diethyl 3-chloroglutaconate (VII). Reaction of VII with hydroxylamine in the presence of sodium hydroxide followed by esterification afforded ethyl 3-hydroxy-5-isoxazoleacetate (IV), which was, after benzenesulfonylation, brominated with NBS to ethyl α-bromo-3-benzenesulfonyloxy-5-isoxazoleacetate (X). Hydrolysis and treatment with ammonia of X gave I. Synthesis of muscimol (II) from IV was also described.
- 社団法人日本薬学会の論文
- 1971-01-25
著者
-
中村 紀雄
New Lead Research Laboratories:sankyo Co. Ltd.
-
中村 紀雄
Central Research Laboratories, Sankyo Co., Ltd.
関連論文
- Synthesis and Antagonistic Activities of Enantiomers of Cyclic Platelet-Activating Factor Analogues
- Lactone and Cyclic Ether Analogues of Platelet-Activating Factor : Synthesis and Biological Activities
- Studies on Acetylenic Compounds. LVI. Syntheses of 4-Isoxazolin-3-ones and 1-Phenyl-3-hydroxypyrazoles
- The Improved Syntheses of dl-Ibotenic Acid and Muscimol
- The Addition Reaction of Diethyl Acetamidomalonate Anion to Ethyl α, β-Dibromoacrylate, and the Base-catalyzed Reactions of the Adduct
- Studies on Acetylenic Compounds. XLIII. Synthesis of Ibotenic Acid.
- Studies on Acetylenic Compounds. XLIV. Synthesis of 3-Aminoisoxazoles and 3-Hydroxyisoxazoles (3-Isoxazolones)
- Studies on Acetylenic Compounds. XLIII. Synthesis of Ibotenic Acid
- Studies on Acetylenic Compounds. XXXIX. The Addition Reaction of Cyanogen Bromide to Acetylenic Compounds