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Synthesis of Hybrid Pharmacophores Based on Adducts of N-Sulfinylaniline and Norbornadiene

Tevs O., Veremeychik Y., Lodochnikova O., Plemenkov V., Litvinov I.

Regioisomeric oximes and thiosemicarbazones derived from 6-substituted pyridoxines

Shtyrlin N., Lodochnikova O., Shtyrlin Y.

Diphosphonioiminobornane diperchlorate: Electrosynthesis, crystal structure, and hydrolysis

Zagumennov V., Sizova N., Lodochnikova O., Krivolapov D., Litvinov I.

Chiral thiophosphorylated thioureas: Synthesis, structure, and cyclization reaction

Metlushka K., Tufatullin A., Shaimardanova L., Sadkova D., Nikitina K., Lodochnikova O., Kataeva O., Alfonsov V.

thioureas were synthesized by the reaction of 2-aminobutan-1-ol and 1-(a-aminobenzyl)-2-naphthol with O,O

Acylated benzothiazinesulfoneamides: Synthesis and molecular structure

Tevs O., Veremeichik Y., Shurpik D., Lodochnikova O., Plemenkov V.

chlorides and anhydrides. X-Ray diffraction data have revealed the presence of an intramolecular С–H···O

Betti base in the synthesis of chiral bisphosphorylated thioureas

Metlushka K., Sadkova D., Nikitina K., Lodochnikova O., Kataeva O., Alfonsov V.

O-phosphorylation

Crystal and Molecular Structure of Acylalmino Derivatives of 1-(2,4,6-Trichlorophenyl)-4,5-dihydropyrazol-5-one

Kataeva O., Litvinov I., Krivolapov D., Lodochnikova O., Abdel-Hafez S., Movchan A., Chmutova G.

Synthesis and antifungal activity of sulfides, sulfoxides, and sulfones based on (1S)-(-)-β-pinene

Gavrilov V., Startseva V., Nikitina L., Lodochnikova O., Gnezdilov O., Lisovskaya S., Glushko N., Klimovitskii E.

Crystal structure of new carboxylate phosphabetaines and phosphonium salts conjugated with them

Bakhtiyarova Y., Aksunova A., Galkina I., Galkin V., Lodochnikova O., Kataeva O.

Stereochemistry of seven-membered heterocycles: XLVII. Synthesis, NMR, XRD, and theoretical investigation of monosulfoxides of (Z)-4,7-dihydro- 1λ4,3-dithiepine series

Galyautdinova A., Vafina R., Kataeva O., Lodochnikova O., Gnevashev S., Gnezdilov O., Gavrilov V., Shtyrlin Y., Chmutova G., Klimovitskii E.

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