Synthesis of macrocarbocycles utilizing intramolecular 1,3-dipolar cycloaddition of nitrile oxides. Synthesis of (.+-.)-muscone.
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概要
- 論文の詳細を見る
Intramolecular 1,3-dipolar cycloaddition of nitrile oxides generated from ω-nitro-1-alkenes gave isoxazoline-fused macrocarbocycles (ring size 12, 14, 15, and 16) in fair to good yields. The 15-membered derivative was converted into (±)-muscone.
- 公益社団法人 日本化学会の論文
著者
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Abe Masayoshi
Department Of Biology Faculty Of Science Shizuoka University
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Asaoka Morio
Department Of Chemical And Biological Sciences Faculty Of Science Japan Women's University
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Takei Hisashi
Department Of Life Chemistry Tokyo Institute Of Technology
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Abe Masayoshi
Department of Life Chemistry, Tokyo Institute of Technology
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- Synthesis of macrocarbocycles utilizing intramolecular 1,3-dipolar cycloaddition of nitrile oxides. Synthesis of (.+-.)-muscone.