116893-45-9Relevant academic research and scientific papers
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 (1988)
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
