Issue 23, 1982

The selective opening of α,β,-epoxyketone trimethylsilyl enol ethers by cuprate reagents: selectivity reversal in tetrahydrofuran

Abstract

Lithium dialkylcuprates in tetrahydrofuran give direct opening of α,β,-epoxyketone trimethylsilyl enol ethers, in contrast to the allylic opening with cuprates reagents in diethyl ether.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1982, 1331-1332

The selective opening of α,β,-epoxyketone trimethylsilyl enol ethers by cuprate reagents: selectivity reversal in tetrahydrofuran

M. F. Schlecht, J. Chem. Soc., Chem. Commun., 1982, 1331 DOI: 10.1039/C39820001331

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