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ВЗАИМОДЕЙСТВИЕ ДИАЛКИЛФОСФИТОВ С КОМПЛЕКСАМИ ПЛАТИНЫ И ПАЛЛАДИЯ И КАТАЛИТИЧЕСКАЯ АКТИВНОСТЬ КОМПЛЕКСОВ МЕТАЛЛОВ 10-й ГРУППЫ В РЕАКЦИИ ПУДОВИКА // Ученые записки КФУ. Естественные науки 2013 том155 N2
Курамшин Аркадий Искандерович, Николаев Андрей Александрович, Черкасов Рафаэль Асхатович, Галкин Владимир Иванович
hydrophosphoryl tautomeric form of a dialkylphosphite
The acidity of the hydroxy-tautomeric form of dimethylphosphite stabilized with chromium group metals
Plotnikova A., Kuramshin A., Galkin V.
) with the dimethylphosphite can afford the organometallic species having the hydroxyl-tautomeric form of the H
The acidity of the hydroxy-tautomeric form of dimethylphosphite stabilized with chromium group metals
Plotnikova A., Kuramshin A., Galkin V.
) with the dimethylphosphite can afford the organometallic species having the hydroxyl-tautomeric form of the H
Stabilization of Hydroxy Tautomeric Form of Dimethyl Phosphite in the Coordination Sphere of Carbonyl Complexes of Group VI Metals
Plotnikova A., Kuramshin A., Kolpakova E., Galkin V.
)pentacarbonyls containing a hydroxy tautomeric form of dimethyl phosphite in the coordination sphere. Hydrogen
Tautomerism of anthraquinones: VIII. Tautomerism and conformations of 1,4-diamino-9,10-anthraquinone
Fain V.Ya., Zaitsev B.E., Ryabov M.A.
,9-diamino-1,10-anthraquinone and tautomeric imino forms, 10-amino-9-hydroxy-1,4-anthraquinone 1-imine
Synthesis and inner-sphere hydrophosphorylation of (η1-N)-N-benzyl-N-(1,3-dimethylbut-2-enylidene)amine-(dicarbonyl)(1,3,5-triorganyl-1,3,5-triazacyclohexane) molybdenum(0) and -tungsten(0)
Kuramshin A., Kolpakova E., Galimullin R., Galkin V.
conditions always involved the addition of the phosphite across the С=N bond to form, depending
Synthesis and inner-sphere hydrophosphorylation of (η1-N)-N-benzyl-N-(1,3-dimethylbut-2-enylidene)amine-(dicarbonyl)(1,3,5-triorganyl-1,3,5-triazacyclohexane) molybdenum(0) and -tungsten(0)
Kuramshin A., Kolpakova E., Galimullin R., Galkin V.
conditions always involved the addition of the phosphite across the С=N bond to form, depending
Anthraquinones tautomerism: VII. Hydroxy-substituted anthraquinones
Fain V.Ya., Zaitsev B.E., Ryabov M.A.
,10-quinoid form, and its ionization involves a tautomeric transformation into 10-oxido-2,9- anthraquinone. β
Tautomeric equilibria as a form of existence of matter. Structure and tautomerism of ametantrone - a medicinal substance of anthraquinone series.
Fine V.Y., Zaitsev B.E., Ryabov M.A.
Ametantrone is not a derivative of 9,10-antraquinone, it exists as a dynamic equilibrium mixture
Tautomerism of the natural anthraquinones physcion and emodin and their analogs
Fain V.Ya., Zaitsev B.E., Ryabov M.A.
anions with a single α-hydroxy that were stabilized by an intramolecular H-bond were formed. Tautomerism

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