Reaction of cyclopropane carboxylic acid derivatives with sulphur tetrafluoride - An example of a diastereoselective ring opening

Z. Hell, Z. Finta, W. Dmowski, F. Faigl, Yu M. Pustovit, L. Tőke, V. Harmat

Research output: Contribution to journalArticle

9 Citations (Scopus)

Abstract

Cyclopropane carboxylic acid derivatives can be converted into trifluoromethyl group-containing compounds using SF4. In the case of a bicyclic cyclopropane carboxylic acid lactone, similar treatment with sulphur tetrafluoride resulted in the cyclopropane ring opening in a diastereoselective manner.

Original languageEnglish
Pages (from-to)297-301
Number of pages5
JournalJournal of Fluorine Chemistry
Volume104
Issue number2
Publication statusPublished - Jul 2000

Fingerprint

cyclopropane
carboxylic acid
Carboxylic acids
carboxylic acids
sulfur
Sulfur
Derivatives
rings
Lactones
cyclopropanecarboxylic acid
sulfur tetrafluoride

Keywords

  • Cyclopropane
  • Ring opening
  • Sulphur tetrafluoride

ASJC Scopus subject areas

  • Inorganic Chemistry
  • Organic Chemistry
  • Materials Chemistry
  • Polymers and Plastics

Cite this

Reaction of cyclopropane carboxylic acid derivatives with sulphur tetrafluoride - An example of a diastereoselective ring opening. / Hell, Z.; Finta, Z.; Dmowski, W.; Faigl, F.; Pustovit, Yu M.; Tőke, L.; Harmat, V.

In: Journal of Fluorine Chemistry, Vol. 104, No. 2, 07.2000, p. 297-301.

Research output: Contribution to journalArticle

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AU - Harmat, V.

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