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Stereochemistry of seven-membered heterocycles: XLVI. Synthesis and dynamic 13C NMR spectroscopy of spiro[cyclohexane-1,4′-[3,5] dioxabicyclo[5.1.0]octanes]. DFT calculations of structurally related formaldehyde and acetone acetals
Gavrilov V., Shamsutdinov M., Chmutova G., Vafina R., Shtyrlin Y., Klochkov V., Klimovitskii E.
Spiro[cyclohexane-1,4′-[3,5]dioxabicyclo[5.1.0]octanes] were synthesized, and their conformational
Stereochemistry of seven-membered heterocycles: XLIII. Steric structure of diastereoisomeric 8,8-dichloro(dibromo)-4-R-3,5-dioxabicyclo[5.1.0]octanes
Baryshnikov R., Vafina R., Fedorenko V., Shtyrlin Y., Klimovitskii E.
.1.0]octanes in good yields. Ultrasonic activation of the process considerably shortened the reaction time
Stereochemistry of seven-membered heterocycles: XLIV. Spatial structure of 4-R-3,5-dioxabicyclo[5.1.0]octanes
Fedorenko V., Baryshnikov R., Khairutdinov B., Vafina R., Shtyrlin Y., Klochkov V., Klimovitskii E.
4-R-3,5-Dioxabicyclo[5.1.0]octanes were prepared in good yields by reduction of the corresponding 8
Synthesis and antimycotic properties of hydroxy sulfides derived from exo- and endo-4-phenyl-3,5,8-trioxabicyclo[5.1.0]octanes
Pavelyev R., Gnevashev S., Vafina R., Gnezdilov O., Dobrynin A., Lisovskaya S., Nikitina L., Klimovitskii E.
Both exo- and endo-isomers of 4-phenyl-3,5,8-trioxabicyclo[5.1.0]octane were reacted
Innovative conceptional approach to quantify the potential benefits of gasoline-methanol blends and their conceptualization on fuzzy modeling
Abdellatief T.M.M., Ershov M.A., Kapustin V.M., Chernysheva E.A., Savelenko V.D., Makhmudova A.E., Potanin D.A., Salameh T., Abdelkareem M.A., Olabi A.G.
, antiknock combustion characteristics of gasoline-methanol blends, involving research octane number (RON
Stereochemistry of seven-membered heterocycles: XLIV. Spatial structure of 4-R-3,5-dioxabicyclo[5.1.0]octanes
Fedorenko V., Baryshnikov R., Khairutdinov B., Vafina R., Shtyrlin Y., Klochkov V., Klimovitskii E.
4-R-3,5-Dioxabicyclo[5.1.0]octanes were prepared in good yields by reduction of the corresponding 8
Stereochemistry of seven-membered heterocycles: XLIII. Steric structure of diastereoisomeric 8,8-dichloro(dibromo)-4-R-3,5-dioxabicyclo[5.1.0]octanes
Baryshnikov R., Vafina R., Fedorenko V., Shtyrlin Y., Klimovitskii E.
.1.0]octanes in good yields. Ultrasonic activation of the process considerably shortened the reaction time
Stereochemistry of seven-membered heterocycles: XLVI. Synthesis and dynamic 13C NMR spectroscopy of spiro[cyclohexane-1,4′-[3,5] dioxabicyclo[5.1.0]octanes]. DFT calculations of structurally related formaldehyde and acetone acetals
Gavrilov V., Shamsutdinov M., Chmutova G., Vafina R., Shtyrlin Y., Klochkov V., Klimovitskii E.
Spiro[cyclohexane-1,4′-[3,5]dioxabicyclo[5.1.0]octanes] were synthesized, and their conformational
Apparent molar volumes and enthalpies of solution of tetracyanoethylene in some solvents and of butan-1-ol in n-octane at different concentrations
Kiselev V., Kashaeva E., Shihaab M., Konovalov A.
and of butan-1-ol in n-octane at different concentrations
Three-component synthesis of bridged 1,3,5-triazinanes
Podrezova A.G., Grudova M.V., Khrustalev V.N., Kvyatkovskaya E.A., Nikitina E.V., Brazhkin V.V., Zubkov F.I.
, and three equivalents of paraformaldehyde, a broad series of 1,3,5-triazabicyco[3.2.1]octanes, 1

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