83748-58-7Relevant academic research and scientific papers
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. XV. "UNSYMMETRICAL" DERIVATIVES OF CINNABARIC ACID - AMPHOLYTES
Plekhanova, N. G.,Glibin, E. N.,Ginzburg, O. F.
, p. 993 - 999 (2007/10/02)
As a result of the joint oxidative condensation of equimolar mixtures of 4-chloro-3-hydroxyanthranilic acid and its amides, containing the β-alanine and ε-aminocaproic acid residue in the amide fragment, with the hydrochloride of N-(2-dimethylaminopropyl)
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
