Issue 5, 1975

Reduction of aryltrimethylsilanes as a synthetic method. Part III. Lithium in ethylamine (Benkeser reduction)

Abstract

Reduction of five aryltrimethylsilanes and one cyclohexenyltrimethylsilane with lithium in ethylamine gives cyclohexanes in every case. Cleavage of one carbon–silicon bond occurs in 1,3-bis(trimethylsilyl)benzene and 1,3,5-tris(trimethylsilyl)benzene. The stereochemistry of the disubstituted cyclohexanes has been assigned.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1975, 475-477

Reduction of aryltrimethylsilanes as a synthetic method. Part III. Lithium in ethylamine (Benkeser reduction)

C. Eaborn, R. A. Jackson and R. Pearce, J. Chem. Soc., Perkin Trans. 1, 1975, 475 DOI: 10.1039/P19750000475

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