1.Anthraquinone-Acridones
First Page
C. F. H. Allen
Chem. Rev., 1959, 59 (6), pp 983–1030
- DOI:
http://dx.doi.org/DOI: 10.1021/cr50030a002
2. Acridone studies. VI. Bromination of acridones in chloroform
RH Prager and HM Thredgold
Abstract
In chloroform and acetic acid, N-methylacridone and methoxylated derivatives rapidly form 1 : 2 adducts with bromine, formulated as hypobromite salts. On gentle warming these decompose to the monobromo substitution product. Hydroxylated acridones appear to also add bromine to the substituted ring, forming products which are highly reactive to water and other nucleophiles.
Australian Journal of Chemistry 22(7) 1503 - 1510
- DOI:
http://dx.doi.org/DOI:10.1071/CH9691503
3. INFLUENCE OF THE REACTION CONDITIONS IN THE N-ALKYLATION OF ACRIDONE-2-CARBOXYLIC ACIDS
Authors: Lisbet Xurez Marill; Rolando F. Pelln Comdom; Miriam Mesa Hernndez
Abstract
The synthesis and a study about the influence of the solvent in the alkylation reaction of 2-Carboxy-6-chloro-9(10H) acridone (3b) and 2-Carboxy-6-chloro-7-nitro-9(10H) acridone (3a) was done, obtaining the N-ethyl ester derivative of the alkylated products. Using the liquid-liquid phase transfer catalysis only the N-alkylated derivative was obtained in both cases with an improved yield.
- DOI:
http://dx.doi.org/DOI: 10.1081/SCC-100104467
Published in: Synthetic Communications, Volume 31, Issue 14 January 2001 , pages 2159 - 2167
Publication Frequency: 24 issues per year
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