Studies on 3-Substituted 1,2-Benzisoxazole Derivatives. V. Electrophilic Substitutions of 1,2-Benzisoxazole-3-acetic Acid
スポンサーリンク
概要
- 論文の詳細を見る
The site of the electrophilic substitution of 1,2-benzisoxazole-3-acetic acid (1) altered depending on species of electrophiles and reaction conditions. In halogenation, only the α-methylene group of 1 was substituted. In the chlorosulfonation, the α-methylene group was substituted at first and then the 5-position of the nucleus was substituted. On the other hand, in the nitration, the 5-position was substituted at first and the α-methylene group was substituted secondly.
- 公益社団法人日本薬学会の論文
- 1978-11-25
著者
-
宇野 準
大日本製薬株式会社総合研究所
-
黒川 美貴雄
Research Laboratories, Dainippon Pharmaceutical Co., Ltd.
-
宇野 準
大日本製薬株式会社
-
宇野 準
大日本製薬
-
宇野 準
Research Laboratory Dainippon Pharmaceutical Co. Ltd.
-
黒川 美貴雄
大日本製薬株式会社創薬研究所
-
宇野 準
Research Laboratories Dainippon Pharmaceutical Co. Ltd.
関連論文
- Nonsteroidal Antiinflammatory Agents. III. : Synthesis of the Metabolites of 10,11-Dihydro-8,α-dimethyl-11-oxodibenz[b, f]oxepin-2-acetic Acid (Bermoprofen)
- 7-アミノデアセトキシセファロスポラン酸の脱硫反応
- Halogenations of S-Benzyl-S-phenylsulfoximides and Base-induced Rearrangements of Their N- and α-Halo Derivatives to N-Sulfinylimines
- Novel Base-Induced Rearrangements of α- and N-Halo Derivatives of S-Ary-S-[(1,2-benzisoxazol-3-yl) methyl] sulfoximides to the Corresponding N-Sulfinylimines
- Halogenation Reaction of S-Aryl-S-[(1,2-benzisoxazol-3-yl) methyl] sulfoximide
- Studies on 3-Substituted 1,2-Benzisoxazole Derivatives. II. The Catalytic Reductions of 1,2-Benzisoxazole-3-acetamide Oxime and Related Compounds
- Studies on 3-Substituted 1,2-Benzisoxazole Derivatives. I
- Synthesis and Biological Activity of 11-[4-(Cinnamyl)-1-piperazinyl]-6,11-dihydrodibenz[b, e]oxepin Derivatives, Potential Agents for the Treatment of Cerebrovascular Disorders
- Sythesis and Stereochemistry of 11-Amino-6,6a, 7,8,9,10,10a, 11-octahydrodibenzo[b, e]thiepines and-oxepines
- An Improved Optical Resolution of 3-Acetylthio-2-methylpropionic Acid by Use of a New Chiral Amine, N-Isopropyl(phenylalaninol)