Issue 15, 1983

Remarkable equatorial selectivity in the aldol coupling between enol silyl ethers and cyclohexanone acetals

Abstract

Lewis acid-catalysed aldol coupling of enol silyl ethers and substituted cyclohexanone acetals shows a markedly higher ratio of equatorial attack than the reaction of the parent ketones.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1983, 796-797

Remarkable equatorial selectivity in the aldol coupling between enol silyl ethers and cyclohexanone acetals

E. Nakamura, Y. Horiguchi, J. Shimada and I. Kuwajima, J. Chem. Soc., Chem. Commun., 1983, 796 DOI: 10.1039/C39830000796

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