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 <i>exo</i>- and <i>endo</i>-4-phenyl-3,5,8-trioxabicyclo[5.1.0]octanes”, Mendeleev Commun., 2012, Volume 22, Issue 3,Pages <nobr>127–128</nobr>

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Mendeleev Commun., 2012 Volume 22, Issue 3, Pages 127–128 (Mi mendc2762)

This article is cited 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. Pavelyev^a, S. G. Gnevashev^a, R. M. Vafina^a, O. I. Gnezdilov^b, A. B. Dobrynin^c, S. A. Lisovskaya^d, L. E. Nikitina^c, E. N. Klimovitskii^a

^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.

Language: English

DOI: 10.1016/j.mencom.2012.05.003

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