N. G. Shikhaliyev, A. M. Maharramov, G. T. Suleymanova, A. A. Babazade, V. G. Nenajdenko, V. N. Khrustalev, A. S. Novikov, A. G. Tskhovrebov, “Arylhydrazones of α-keto esters via methanolysis of dichlorodiazabutadienes: synthesis and structural study”, Mendeleev Commun., 31:5 (2021), 677

Эта публикация цитируется в 8 статьях

Communications

Arylhydrazones of α-keto esters via methanolysis of dichlorodiazabutadienes: synthesis and structural study

N. G. Shikhaliyev^a, A. M. Maharramov^a, G. T. Suleymanova^a, A. A. Babazade^a, V. G. Nenajdenko^b, V. N. Khrustalev^cd, A. S. Novikov^e, A. G. Tskhovrebov^df

^a Department of Chemistry, Baku State University, Baku, Azerbaijan
^b Department of Chemistry, M.V. Lomonosov Moscow State University, Moscow, Russian Federation
^c N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
^d Peoples Friendship University of Russia (RUDN University), Moscow, Russian Federation
^e Institute of Chemistry, St. Petersburg State University, St. Petersburg, Russian Federation
^f N.N. Semenov Federal Research Center for Chemical Physics, Russian Academy of Sciences, Moscow, Russian Federation

Аннотация: Novel approach to methyl 2-aryl-2-(arylhydrazono) acetates via methanolysis of dichlorodiazabutadienes was developed. Hydrogen bonding in methyl Z-2-phenyl-2-(phenyl-hydrazono) acetate was explored by DFT calculations and topological analysis of the electron density distribution within the framework of Bader’s theory (QTAIM method).

Ключевые слова: keto esters, hydrazones, hydrogen bonding, DFT, QTAIM, calculations, methanolysis.

Язык публикации: английский

DOI: 10.1016/j.mencom.2021.09.028

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