51952-50-2Relevant academic research and scientific papers
Electrochemical Synthesis of Bi-1,4-naphthoquinonyl Derivatives
Schutte, J. Harm P.,Plessis, Jan A. K. du,Lachmann, Gerhard,Viljoen, Agatha M.,Nelson, Hendrik D.
, p. 1290 - 1291 (1989)
Electrolysis of 1,4-naphthoquinone derivatives with magnesium perchlorate as supporting electrolyte in aqueous acetic acid has led to oxidative dimerization of the quinone and is a new, convenient, and selective method of preparation of 2,2'-bi-1,4-naphthoquinonyl derivatives.
Palladium catalyzed Carbon–Hydrogen bond activation on amino-substituted quinones under acidic condition
Huang, Peng-Hao,Hong, Rui-Yu,Hong, Fung-E
, p. 2337 - 2347 (2021/10/08)
In this study, 2-(benzylamino)naphthalene-1,4-dione (4a) was used as the starting material to carry out a one-pot catalytic reaction in acetic acid with divalent palladium metal Pd(OAc)2 in a nitrogen atmosphere. Two compounds, 5a and 6a, were observed unexpectedly. Both compounds were characterized by spectroscopic methods as well as X-ray single crystal determination. The crystal structure of 5a reveals that a nitrogen-containing six-membered ring is formed; while the crystal structure of 6a shows that both oxazole and pyridine ring are generated. The optimized condition for making 6a was pursued. Derivatives of 4a, such as 4b and 4c, were also used as starting materials to proceed under the aforementioned optimal reaction conditions. Although the yields are not satisfactory, obviously the same patterns of corresponding compounds can be synthesized. The reaction of a 4a-structural related compound 9 under similar condition, two unexpected oxazole-containing compounds, 10 and 11, were obtained. The diverse pathways for this type of reactions even starting with slightly different substituents on the quinone indeed provides chemists with a perpetual motivation for further studies.
PHOTOLYSIS OF 2-AMINO- AND 2-METHYLAMINO-1,4-NAPHTHOQUINONE
Martins, F. J. C.,Viljoen, A. M.,Strydom, S. J.,Fourie, L.,Wessels, P. L.
, p. 591 - 598 (2007/10/02)
Pyrex-filtered sunlight irradiation of solutions of 2-amino-1,4-naphthoquinone unexpedtedly failed to produce cyclobutane dimers.Irradiation in acetic anhydride led to the formation of the trimeric 6--dibenzocarbazole-5,13:7,12-diquinone as well as 3,3'-diamino-2,2'-bi-carbazole-5,13:7,12-diquinone.Similar treatment of 2-methylamino-1,4-naphthoquinone afforded 6--dibenzocarbazole-5,13:7,12-diquinone and 6-methyl-dibenzocarbazole-5,13:7,12-diquinone
