Chemistry of Heterocyclic Compounds p. 544 - 548 (1981)
Update date:2022-08-05
Topics:
Orlov, V. D.
Kolos, N. N.
Rozhko, L. I.
Yaremenko, F. G.
Zolotarev, B. M.
Lavrushin, V. F.
The reaction of o-aminophenol with 4- and 4'-substituted chalcones and benzalacetones in methanol (with a tertiary amine as the catalyst), which leads to products of β addition of 2-aminophenoxazin-3-one to the C=C bond of an unsaturated ketone, was investigated.The activating role of the unsaturated ketone in the formation of a phenoxazine fragment was examined.The structures of the synthesized compounds were confirmed by IR, UV, PMR, and mass spectrometry.
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Doi:10.1002/jps.2600700803
(1981)Doi:10.1021/jo00339a026
(1981)Doi:10.1039/P19810002253
(1981)Doi:10.1039/d0md00049c
(2020)Doi:10.1039/c39810001269
(1981)Doi:10.1021/ol048462v
(2004)
