1, 3-dipolar addition of nitrile oxides to 3a, 4-dihydro-1-isoindolinones
スポンサーリンク
概要
- 論文の詳細を見る
1,3-Dipolar addition of acetonitrile oxide to 2-phenyl-3a,4-dihydro-1-isoindolinone was carried out in a stereoselective but regiorandam manner. However, the introduction of substituent, e. g., methyl group, at the 4-position of the 1H-isoindol-1-one system turned out to improve regioselectivity of the addition. The regio- and stereoselective isoxazoline synthesis was also accomplished in the reaction with other nitrile oxides. The transformation of the isoxazoline ring was also examined.
- 山口大学の論文
著者
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NOGUCHI Michihiko
Department of Applied Chemistry and Chemical Engineering
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Noguchi Michihiko
Department Of Industrial Chemistry
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Kajigaeshi Shoji
Department Of Applied Chemistry And Chemical Engineering Faculty Of Engineering Yamaguchi University
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Kakimoto Shinji
Department Of Industrial Chemistry
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