Issue 20, 1989

Folding strain control for remote stereocontrol: diastereoselectivity in the ring closure reactions of 2-(6′-trimethylsilylhex-4′-enyl)cyclohex-2-enones with alkyl groups at various positions in the side chain

Abstract

The general utility of the folding strain control concept for remote stereocontrol has been examined in the ring closure reaction of 2-(6′-trimethylsilylhex-4′-enyl)cyclohex-2-enones with various alkyl-substituted side chains.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1989, 1572-1573

Folding strain control for remote stereocontrol: diastereoselectivity in the ring closure reactions of 2-(6′-trimethylsilylhex-4′-enyl)cyclohex-2-enones with alkyl groups at various positions in the side chain

T. Tokoroyama, K. Okada and H. Iio, J. Chem. Soc., Chem. Commun., 1989, 1572 DOI: 10.1039/C39890001572

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