Chemistry of Heterocyclic Compounds p. 155 - 158 (1982)
Update date:2022-08-03
Topics:
Grinev, A. N.
Ryabova, S. Yu.
The reaction of N-acetylindoxyl hydrazone with ketones in alcohol gave N-acetylindoxyl alkylidenehydrazones, which were converted to pyrrolo<3,2-b>indole derivatives by treatment with glacial acetic acid.Pyrrole<3,2-b>indole derivatives were also obtained in the reaction of N-acetylindoxyl hydrazone with ketones in glacial acetic acid.The structures of the synthesized products were confirmed by data from the IR, UV, PMR, and mass spectra.
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Doi:10.1021/jo048605r
(2004)Doi:10.1002/cjoc.201180269
(2011)Doi:10.1021/ic00138a060
(1982)Doi:10.1002/jhet.5570210132
(1984)Doi:10.1016/0040-4020(81)85013-2
(1981)Doi:10.1016/S0040-4039(01)83015-X
(1981)
