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NUCLEOTIDE COMPOSITION AND HOMOLOGY OF DNA IN PARASITIC LEPTOSPIRAE
EZHOV G.I., ARTYUSHIN S.K., LYSENKO A.M.
Polarity and structure of P(X)-modified (X = O, S) arylcarbamoylmethylphosphine oxides and sulfides
Vereshchagina Y., Khanafieva R., Chachkov D., Artyushin O., Sharova E., Ishmaeva E.
of several rotational isomers stabilized by H · · · X intramolecular hydrogen bonds (X = O, S). The most
Polarity and structure of P(X)-modified (X = O, S) arylcarbamoylmethylphosphine oxides and sulfides
Vereshchagina Y., Khanafieva R., Chachkov D., Artyushin O., Sharova E., Ishmaeva E.
of several rotational isomers stabilized by H · · · X intramolecular hydrogen bonds (X = O, S). The most
Synthesis, polarity, and structure of 2-chloro-N-[2-(methylsulfanyl)phenyl]- and 2-(diphenylthiophosphoryl)-N-[2-(methylsulfanyl)phenyl]acetamides
Ishmaeva E., Alimova A., Vereshchagina Y., Chachkov D., Artyushin O., Sharova E.
to exist as an equilibrium mixture of two conformers with synclinal and anticlinal orientations of the {C-{s
Conformational analysis of 2-aminophenyl-, 2-aminobenzyl-, and 2-nitrobenzyl(diphenyl)phosphine oxides
Vereshchagina Y., Alimova A., Chachkov D., Ishmaeva E., Artyushin O., Sharova E., Klimovitskii A., Khanafieva R.
Polarity and structure of diphosphorus-substituted isoxazole and 1,2,3-triazole
Vereshchagina Y., Alimova A., Sharova E., Artyushin O., Chachkov D., Ishmaeva E.
Synthesis, polarity, and structure of 2-chloro-N-[2-(methylsulfanyl)phenyl]- and 2-(diphenylthiophosphoryl)-N-[2-(methylsulfanyl)phenyl]acetamides
Ishmaeva E., Alimova A., Vereshchagina Y., Chachkov D., Artyushin O., Sharova E.
to exist as an equilibrium mixture of two conformers with synclinal and anticlinal orientations of the {C-{s
Conformational Analysis of 2-Chloro- N-[2-((Diphenylphosphoryl)Methyl)Phenyl]-Acetamide and 2-Chloro-N-[2-((Diphenylthiophosphoryl)Methyl)Phenyl]Acetamide
Vereshchagina Y., Alimova A., Chachkov D., Khanafieva R., Artyushin O., Ishmaeva E.
. The formation of intramolecular hydrogen bond P=O⋯HN or P=S⋯HN in these acetamides is possible.
Conformational Analysis of 2-Chloro- N-[2-((Diphenylphosphoryl)Methyl)Phenyl]-Acetamide and 2-Chloro-N-[2-((Diphenylthiophosphoryl)Methyl)Phenyl]Acetamide
Vereshchagina Y., Alimova A., Chachkov D., Khanafieva R., Artyushin O., Ishmaeva E.
. The formation of intramolecular hydrogen bond P=O⋯HN or P=S⋯HN in these acetamides is possible.
3-Aryl(hetaryl)-3-hydroxy-2-phosphorus-substituted acrylonitriles. Synthesis and experimental and theoretical conformational analysis
Odinets I., Vereshchagina Y., Artyushin O., Kalyanova R., Mastryukova T., Ishmaeva E., Fattakhova G., Chachkov D., Yarkova E.
-chemical calculations [B3LYP/6-31G(d)]. The C=C double bond and the phosphoryl or thiophosphoryl group have an s

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