Synthesis and autoconversions of furanthiols and -selenols

Authors

  • B. Ю. Введенский Irkutsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, Irkutsk
  • E. Д. Штефан Irkutsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, Irkutsk
  • P. Н. Малюшенко Irkutsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, Irkutsk
  • Э. Н. Дерягина Irkutsk Institute of Organic Chemistry, Siberian Branch, Russian Academy of Sciences, Irkutsk

Abstract

Furanthiols and selenols have been synthesized by a modified procedure via organolithium derivatives, with the formation of trimethylsilyl ethers as intermediate products. It has been shown that the thiols as well as the selonols undergo autoconversions when standing in air and in the presence of triethylamine with the formation of furylthio(seleno)-substituted thio(seleno)butyrolactones.

How to Cite
Vvedenskii, V. Y.; Shtefan, E. D.; Malyushenko, R. N.; Deryagina, É. N. Chem. Heterocycl. Compd. 1994, 30, 767. [Khim. Geterotsikl. Soedin. 1994,891.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01169630

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Published

1994-07-25

Issue

No. 7 (1994)

Section

Original Papers