Chemistry Letters p. 2075 - 2078 (1984)
Update date:2022-08-02
Topics:
Kubo, Yasuo
Tojo, Sachiko
Suto, Manami
Toda, Rie
Araki, Takeo
Photolyses of N-methylnaphthalenedicarboximides (1,8-NI, 2,3-NI, and 1,2-NI) with various olefins were investigated in benzene.The reaction pathways depended largely on the structure of arene moiety of the imides.The main reactions of 1,8-NI, 2,3-NI, and 1,2-NI were found as cyclobutane formation, oxetane formation, and insertion of olefin between the C(=O)-N bond of imide moiety, respectively.
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