Khazhiev, S.Y.,
Khusainov, M.A.,
Khalikov, R.A.,
Tyumkina, T.V.,
Meshcheryakova, E.S.,
Khalilov, L.M.,
Kuznetsov, V.V. (2018) , 13С NMR spectroscopy and X-
ray analysis. The molecule exists in the chair conformation
Kuramshina, A.E.,
Khalikov, R.A.,
Kataev, V.A.,
Tyumkina, T.V.,
Meshcheryakova, E.S.,
Khalilov, L.M.,
Kuznetsov, V.V. (2020) and X-
ray analysis. Its molecules in crystal, as well as inCDCl3 andC6D6 solutions, have achair
Talybov, Rustam,
Beylerli, Ozal,
Mochalov, Vadim,
Prokopenko, Alexey,
Ilyasova, Tatiana,
Trofimova, Tatiana,
Sufianov, Albert,
Guang, Yang (2022) tomograph, a Canon Aquilion
One multispiral X-
ray computed tomograph (Gadovist 7.5 ml, Yomeron 400 mg−50 ml
KHAZHIEV, S.Y.,
KHUSAINOV, M.A.,
KUZNETSOV, V.V.,
KHALIKOV, R.A.,
KATAEV, V.A.,
TYUMKINA, T.V.,
MESHCHERYAKOVA, E.S.,
KHALILOV, L.M. (2020) spectroscopy and X-
ray analysis. Its molecules in crystal adopt a chair conformation, whereas equilibrium
KHAZHIEV, S.Y.,
KHUSAINOV, M.A.,
KUZNETSOV, V.V.,
KHALIKOV, R.A.,
TYUMKINA, T.V.,
MESHCHERYAKOVA, E.S.,
KHALILOV, L.M. (2019) of 1H and 13C NMR spectroscopy as well as X-
ray diffraction analysis. The molecules of compound 1 exist