Тиетанильная защита в синтезе 5-арилокси (сульфонил) -3-бром-1,2,4-триазоловKhaliullin, F.A.,
Klen, E. E.,
Makarova, N. N.,
Халиуллин, Ф.А.,
Клен, Э.,
Макарова, Н. Н. (2018) , nucleophilic substitution of the 5-bromine
atom by phenoxy or phenylsulfanyl group, oxidation of the thietane
Khaliullin, F.A.,
Shabalina, Y.V.,
Samorodov, A.V.,
Kamilov, F.K.,
Timirkhanova, G.A.,
Murataev, D.Z. (2018) spectroscopy data. The compounds synthesized here had potentially high antiaggregatory activity.
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
AKHMETOVA, V.R.,
AKHMADIEV, N.S.,
NURTDINOVA, G.M.,
GALIMOVA, R.A.,
GALIMOVA, A.M.,
AGLETDINOV, E.F.,
KATAEV, V.A.,
KHISAMUTDINOV, R.A. (2018) spectroscopy, mass-spectrometry and Xray diffraction. The biological activity of the combinatorial series
Koltygin, A.,
Bazhenov, V.,
Komissarov, A.,
Khasenova, R.,
Anishchenko, A.,
Fozilov, B.,
Bautin, V.,
Seferyan, A.,
Bilyalov, A. (2018) determined using scanning electron microscopy and energy dispersive X-ray
spectroscopy. The phase diagrams