Issue 2, 1990

Synthesis of ethynyl(phenyl)iodonium tetrafluoroborate. A new reagent for ethynylation of 1,3-dicarbonyl compounds

Abstract

Hydrogen fluoride-induced protiodetrimethylsilylation of trimethylsilylethynyl(phenyl)iodonium tetrafluoroborate (5), prepared from bis(trimethylsilyl)ethyne (4), affords ethynyl(phenyl)iodonium tetrafluoroborate (1), a reagent for α-ethynylation of β-dicarbonyl compounds under mild conditions.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1990, 118-119

Synthesis of ethynyl(phenyl)iodonium tetrafluoroborate. A new reagent for ethynylation of 1,3-dicarbonyl compounds

M. Ochiai, T. Ito, Y. Takaoka, Y. Masaki, M. Kunishima, S. Tani and Y. Nagao, J. Chem. Soc., Chem. Commun., 1990, 118 DOI: 10.1039/C39900000118

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