3712-09-2Relevant articles and documents
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Harris,W.M.,Geissman,T.A.
, p. 432 - 434 (1965)
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Copper bromide-catalyzed c-alkylation of 2-amino-1,4-naphthoquinone: New synthesis of 1-azaanthraquinones
Tapia, Ricardo A.,Venegas, Juan,Cantuarias, Lorena B.
experimental part, p. 151 - 156 (2010/03/24)
Copper(I) bromide catalyzes the regioselective Michael addition reaction of 2-amino-1,4-naphthoquinone (5) with methyl vinyl ketone and 2-propenal to provide easy access to C-alkylated quinone derivatives, useful precursors of 1-azaanthraquinones.
Synthesis of Quinolinequinones and 1,2,3,4-Tetrahydroquinolinequinones via Cyclobutenediones
Liebeskind, Lanny S.,Zhang, Jing
, p. 6379 - 6385 (2007/10/02)
N-Benzyl-1,2,3,4-tetrahydrocyclobutapyridine-5,6-dione is easily synthesized and functions as a synthetic equivalent of the unstable pyridiocyclobutenedione.Regiospecific introduction of unsaturated nucleophiles at the more reactive carbonyl group, followed by thermolysis in xylene in vessels open to air, rapidly establishes the tetrahydroquinolinequinone system which can be oxidized to the corresponding quinolinequinone with 2,3-dichloro-5,6-dicyanoquinone.
