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Study of the spatial structure of the chloroanhydride of dichloromethylphosphonic acid by a combination of various physical methods
Raevskii O., Khalitov F., Mumzhieva N., Gilyazov M., Zakirov D., Safin I., Aganov A.
and gauche-trans orientation of the two CHCl2 group chlorines with respect to the P=O bond). The conformers
Study of the spatial structure of the chloroanhydride of dichloromethylphosphonic acid by a combination of various physical methods
Raevskii O., Khalitov F., Mumzhieva N., Gilyazov M., Zakirov D., Safin I., Aganov A.
and gauche-trans orientation of the two CHCl2 group chlorines with respect to the P=O bond). The conformers
Conformations of acyclic sulfites
Yuldasheva L., Timosheva A., Remizov A., Sergeeva G., Fishman A., Vereshchagin A.
-trans- and trans-gauche-conformations of the chain R-O-S-O-R. 2. Diaryl sulfites exist in a trans-gauche
Spatial structure of α-halogen-substituted sulfones
Bumenko G., Vereshchagin A., Lyakisheva L.
1. Conformational equilibrium between the gauche- and trans-forms is attained in α
Three-dimensional structures of phosphorus-containing heterocycles. Communication 35. 2-Phenoxy-2-oxo-1,3,2-oxaselenaphosphorinanes
Arshinova R., Ovodova O., Danilova O., Nuretdinova O., Samitov Y., Arbuzov B.
orientation of the aroxy grouping; the aryl group occupies a gauche orientation with respect to the P=O bond
Особенности организации лексических групп предметно-бытовой лексики
Гауч, О. Н., Gauch, O. N.
Dipole moments and conformations of 2-(4-pyridyl) ethyl aryl selenides and 2-(4-pyridyl)ethyl aryl sulfones with two nonidentical geminal axes of internal rotation
Samarina O., Abdullina N., Ishmaeva E., Pudovik A.
and gauche C-Py and C-Se fragment orientations, the latter predominant; conformational equilibrium
Experimental and Theoretical Conformational Analysis of Tris(4-methylphenyl)phosphine and Its Chalcogenides
Kuznetsova A.A., Ismagilova R.R., Chachkov D.V., Belogorlova N.A., Malysheva S.F., Vereshchagina Y.A.
in solution as a single symmetricalconformer with gauche,gauche,gauche orientation ofthe substituents
The geometrical structures of phosphorus-containing heterocycles 20. 1,3,2-Dioxaphosphorinanes with two geminal axes of internal rotation
Arbuzov B., Kataev V., Arshinova R., Gubaidullin R.
of conformera with trans-gauche and gauche-gauche orientations of the Br-C-C5-C-Br chain (the first index refers
Polarity and Conformational Analysis of Tri(1-naphthyl)phosphine, Tri(2-naphthyl)phosphine, and Their Chalcogenides
Kuznetsova A.A., Chachkov D.V., Belogorlova N.A., Kuimov V.A., Malysheva S.F., Vereshchagina Y.A.
single conformer with a gauche,gauche,gauche orientation of the substituents at the phosphorus. Tri(2

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