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Syngas as a synergistic reducing agent for selective reductive amination—a mild route to bioactive amines
Podyacheva E., Balalaeva A.I., Afanasyev O.I., Runikhina S.A., Chusova O., Kozlov A.S., Liao S., Chusov D.
, or are not atom-economical. The application of syngas as a mild and selective reducing agent to aminate carbonyl
Tris(2,6-dimethoxyphenyl)methyl carbenium ion as a charge derivatization agent for the analysis of primary amines by MALDI mass spectrometry
Topolyan A.P., Strizhevskaya D.A., Slyundina M.S., Belyaeva M.A., Ivanova O.M., Korshun V.A., Ustinov A.V., Mikhura I.V., Formanovsky A.A., Borisov R.S.
A novel derivatization method for the analysis of primary amines by MALDI mass spectrometry
Reductive amination catalyzed by iridium complexes using carbon monoxide as a reducing agent
Moskovets A.P., Usanov D.L., Afanasyev O.I., Fastovskiy V.A., Molotkov A.P., Muratov K.M., Denisov G.L., Zlotskii S.S., Smol'Yakov A.F., Loginov D.A., Chusov D.
Development of novel, sustainable catalytic methodologies to provide access to amines represents a
Hydrogen-free reductive amination using iron pentacarbonyl as a reducing agent
Afanasyev O.I., Usanov D.L., Chusov D.
We developed solvent-free reductive amination without an external hydrogen source using iron
Electrochemical amination of benzene in aqueous solutions of sulfuric acid and an organic solvent
Lisitsyn Y., Kargin Y.
on solvents to be used in indirect cathodic amination of aromatic compounds. They improve the aromatic
Synthetic Access to Secondary Propargylamines via a Copper-Catalyzed Oxidative Deamination/Alkynylation Cascade
Li H., Feng H., Zhang J., Huang L., Van Der Eycken E.V.
A novel and selective cascade reaction of primary amines and alkynes for the synthesis
Indenyl rhodium complexes. Synthesis and catalytic activity in reductive amination using carbon monoxide as a reducing agent
Runikhina S.A., Arsenov M.A., Kharitonov V.B., Sovdagarova E.R., Chusova O., Nelyubina Y.V., Denisov G.L., Usanov D.L., Chusov D., Loginov D.A.
of alkylated amines via catalytic reductive amination using carbon monoxide as a reducing agent. Water as a
Electrochemical amination in the system Ti(IV)-NH 2OH-C 6H 6: The efficiency of the process in a sulfuric acid solution containing an organic solvent
Lisitsyn Y., Kargin Y.
permits the production of aromatic amines with the overall yield by hydroxylamine reaching 91%. Due to a
Diastereoselectivity of Azido-Ugi Reaction with Secondary Amines. Stereoselective Synthesis of Tetrazole Derivatives
Zarezin D.P., Khrustalev V.N., Nenajdenko V.G.
isolated in excellent yields (≤98%). The reaction has a broad scope in terms of its amine, aldehyde
Reductive Amination in the Synthesis of Pharmaceuticals
Afanasyev O.I., Kuchuk E., Usanov D.L., Chusov D.
Reductive amination plays a paramount role in pharmaceutical and medicinal chemistry owing to its

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