Journal of Heterocyclic Chemistry p. 1909 - 1913 (1996)
Update date:2022-08-05
Topics:
Yoneda, Ryuji
Kimura, Tetsuya
Kinomoto, Junko
Harusawa, Shinya
Kurihara, Takushi
Ring expansion of azetopyridoindole 11 via the [1,2]-Meisenheimer rearrangement of the corresponding N-oxide 12 gave azocinoindole 14, which was converted into the N-benzoylenaminone 18 in 5 steps. Intramolecular cyclization of 18 was accomplished by a mo
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Doi:10.1021/ja01111a045
(1953)Doi:10.1016/S0008-6215(96)00211-X
(1996)Doi:10.1021/ja9636404
(1997)Doi:10.1002/jhet.5570330645
(1996)Doi:10.1016/j.bmc.2004.03.028
(2004)Doi:10.1039/c3cc47830k
(2014)
