Issue 17, 1995

Carbon–carbon bond formation and reduction of aldehydes, ketones and acetals with silylated nucleophiles catalysed by tetracyanoethylene

Abstract

Tetracyanoethylene catalyses the reactions of aldehydes, ketones and acetals with silylated nucleophiles such as trimethylsilyl cyanide, allyltrimethylsilane, aryl methyl ketone trimethylsilylenol ethers and triethylsilane to promote carbon–carbon bond formation and reduction under neutral conditions. All the evidence strongly suggested that the reactions occur through single electron transfer (SET) mechanism based on UV spectroscopic measurements.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1995, 2155-2158

Carbon–carbon bond formation and reduction of aldehydes, ketones and acetals with silylated nucleophiles catalysed by tetracyanoethylene

T. Miura and Y. Masaki, J. Chem. Soc., Perkin Trans. 1, 1995, 2155 DOI: 10.1039/P19950002155

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