Diaryldiacyloxyspirosulfuranes-I. Syntheses from sulfides with halogenating agents

I. Kapovits, J. Rábai, F. Ruff, Á Kucsman

Research output: Contribution to journalArticle

31 Citations (Scopus)

Abstract

A series of diaryldiacyloxyspirosulfuranes has been prepared from bis(2-carboxyaryl) sulfides with different halogenating agents. In pyridine, sulfides with two electron-withdrawing nitro groups cannot be converted into spirosulfuranes, suggesting the participation of pyridine in Cl+-transfer reactions. UV and IR spectroscopic data for spirosulfuranes are also reported and briefly discussed.

Original languageEnglish
Pages (from-to)1869-1874
Number of pages6
JournalTetrahedron
Volume35
Issue number15
DOIs
Publication statusPublished - 1979

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Sulfides
Electrons
pyridine

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Diaryldiacyloxyspirosulfuranes-I. Syntheses from sulfides with halogenating agents. / Kapovits, I.; Rábai, J.; Ruff, F.; Kucsman, Á.

In: Tetrahedron, Vol. 35, No. 15, 1979, p. 1869-1874.

Research output: Contribution to journalArticle

Kapovits, I. ; Rábai, J. ; Ruff, F. ; Kucsman, Á. / Diaryldiacyloxyspirosulfuranes-I. Syntheses from sulfides with halogenating agents. In: Tetrahedron. 1979 ; Vol. 35, No. 15. pp. 1869-1874.
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