81325-74-8Relevant academic research and scientific papers
Synthesis of Actinomycin Analogs: XXII. Lipointercalants on the Basis of Actinocin
Glibin, E. N.,Popova, E. B.
, p. 384 - 387 (2007/10/03)
Joint oxidative condensations of N-alkyl-3-hydroxyantranilamide with N-(3-dimethylaminopropyl)-4-methyl-3-hydroxyanthranilamide hydrochloride gave 6-demethylactinocin diamides containing C4H9, cyclo-C6H11, C12H25, or C18H37 group in the α-amide group and 3-(dimethylammonio)propyl radical in the β-amide group.
OXIDATION OF ORTHO-AMINOPHENOLS III. THE JOINT OXIDATION OF DERIVATIVES OF 3-HYDROXYANTHRANILIC ACID DIFFERING IN THE SUBSTITUENTS AT POSITION 4
Korshunova, Z. I.,Popova, E. B.,Glibin, E. N.,Ginzburg, O. F.
, p. 314 - 319 (2007/10/02)
The joint oxidation of 3-hydroxyanthranilic acid and its 4-methoxy-substituted derivative and also the amides of 3-hydroxyanthranilic acid and the amide of 4-chloro-3-hydroxyanthranilic acid with the amides of 4-methyl-3-hydroxyanthranilic acid always lea
SYNTHESIS OF ACTINOMYCIN ANALOGS XIII. UNSYMMETRICAL DERIVATIVES OF CINNABARIC ACID
Tsukerman, B. V.,Glibin, E. N.,Ginzburg, O. F.
, p. 1503 - 1508 (2007/10/02)
During the oxidation of mixtures of substituted 2-amino-3-hydroxy-4-methylbenzamides with the ester or amide of 2-amino-3-hydroxy-4-chlorobenzoic acid the formation of the 2-amino-4,6-dimethyl-3H-3-oxophenoxazine derivative is suppressed by the increase i
