SYNTHESIS AND FUNCTIONALIZATION OF 7-HYDROXYANTHRA[2,1-<i>b</i>]BENZO[<i>d</i>]FURAN-8,13-DIONES
DOI:
https://doi.org/10.1007/3034Keywords:
anthraquinones, benzofurans, quinone diazide, diazotizationAbstract
The diazotization of 1-amino-2-aryloxy-4-hydroxy-9,10-anthraquinones in various solvents and subsequent heating of the diazotization products lead to 7-hydroxyanthra[2,1-b]benzo[d]furan-8,13‑diones. When consecutively treated with benzenesulfonyl chloride and amines, the products form 7‑aminoanthra[2,1-b]benzo[d]furan-8,13-diones.
How to Cite
Gornostaev, L. M.; Arnold, E. V.; Lykova, E. V.; Sadoschenko, M. V. Chem. Heterocycl. Compd. 2010, 46, 665. [Khim. Geterotsikl. Soedin. 2010, 832.]
For this article in the English edition see DOI 10.1007/s10593-010-0566-2