Chemistry of Heterocyclic Compounds p. 811 - 813 (1982)
Update date:2022-07-29
Topics:
Zhungietu, G. I.
Zorin, L. M.
Gorgos, V. I.
Rekhter, M. A.
5H-Pyridazo<4,5-b>indol-1-ones were obtained by heating 2-acetylindole-3- or 2-aroylindole-3-carboxylic acids with hydrazine hydrate in ethylene glycol or alcohol. 1-Chloro-5H-pyridazo<4,5-b>indoles are formed by treatment of 5H-pyridazo<4,5-b>indol-1-one
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Doi:10.1246/cl.1982.1525
(1982)Doi:10.1002/anie.201700417
(2017)Doi:10.1007/PL00007262
(1951)Doi:10.1007/BF00952389
(1982)Doi:10.1016/0040-4020(95)00635-L
(1995)Doi:10.1021/jm00358a027
(1983)
