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This article is cited in 12 scientific papers (total in 12 papers)
Synthesis and Antimycotic Properties of Hydroxy Sulfides Derived from exo- and endo-4-phenyl-3,5,8-trioxabicyclo[5.1.0]octanes
R. S. Pavelyeva, S. G. Gnevasheva, R. M. Vafinaa, O. I. Gnezdilovb, A. B. Dobryninc, S. A. Lisovskayad, L. E. Nikitinac, E. N. Klimovitskiia a Alexander Butlerov Institute of Chemistry, Kazan Federal University, Kazan, Russian Federation
b E.K. Zavoisky Physical-Technical Institute, Kazan Scientific Center, Russian Academy of Sciences, Kazan, Russian Federation
c A.E. Arbuzov Institute of Organic and Physical Chemistry, FRC Kazan Scientific Center of the Russian Academy of Sciences, Kazan, Russian Federation
d Kazan Research Institute of Epidemiology and Microbiology, Kazan, Russian Federation
Abstract:
Both exo- and endo-isomers of 4-phenyl-3,5,8-trioxabicyclo[5.1.0]octane were reacted with thiophenol to afford individual diastereomers of hydroxy sulfides which were further processed in search for new antimycotic substances.
Citation:
R. S. Pavelyev, S. G. Gnevashev, R. M. Vafina, O. I. Gnezdilov, A. B. Dobrynin, S. A. Lisovskaya, L. E. Nikitina, E. N. Klimovitskii, “Synthesis and Antimycotic Properties of Hydroxy Sulfides Derived from exo- and endo-4-phenyl-3,5,8-trioxabicyclo[5.1.0]octanes”, Mendeleev Commun., 22:3 (2012), 127–128
Linking options:
https://www.mathnet.ru/eng/mendc2762 https://www.mathnet.ru/eng/mendc/v22/i3/p127
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