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Mendeleev Communications, 2012, Volume 22, Issue 3, Pages 127–128
DOI: https://doi.org/10.1016/j.mencom.2012.05.003
(Mi mendc2762)
 

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.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (258.2 Kb)


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
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  • https://www.mathnet.ru/eng/mendc/v22/i3/p127
  • This publication is cited in the following 12 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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