A spectral study of tautomerism in 4-arylamino-1,2-naphthoquinones
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference14 articles.
1. THE TAUTOMERISM OF HYDROXY QUINONES
2. A Study of the Addition Reactions of Certain Alkylated Naphthoquinones1
3. NMR spectra of intramolecularly hydrogen-bonded compounds—II
4. Nuclear Magnetic Resonance Studies of Keto-enol Equilibria. III. α,β-Unsaturated-β-Ketoamines
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1. 1,2-Naphthoquinone-4-sulfonic acid salts in organic synthesis;Beilstein Journal of Organic Chemistry;2022-01-05
2. Isomerization of 4-arylamino-1,2-naphthoquinones to 2-arylamino-1,4-naphthoquinones;Russian Chemical Bulletin;2017-06
3. Cyclization of 2-(3-R-prop-2-ynyloxy)-4-phenyliminonaphthalen- 1(4H)-ones into 2-R-methylidene-6-phenylamino-2,3-dihydronaphtho[2,1-b]-1,4-dioxines;Mendeleev Communications;2016-07
4. “Ligands-with-Benefits”: Naphthalene-Substituted Schiff Bases Yielding New NiII Metal Clusters with Ferromagnetic and Emissive Properties and Undergoing Exciting Transformations;Inorganic Chemistry;2016-01-20
5. On the reactivity of benzo[a]phenazine-5,6-dione 7-oxides with methanolic alkali and pyrrolidine;Chemistry of Heterocyclic Compounds;2015-02
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