Issue 6, 1993

A probe of Cieplak's proposal: effect of 2-axial substitution on reactivity in the LiAlH4 reduction of cyclohexanones

Abstract

The relative reactivities of cyclohexanones in which the 2-axial position is substituted by methyl or methoxy group in LiAlH4 reduction strongly support the Cieplak model which focuses on the importance of stabilisation of the transition state by antiperiplanar allylic bonds.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1993, 1009-1010

A probe of Cieplak's proposal: effect of 2-axial substitution on reactivity in the LiAlH4 reduction of cyclohexanones

Y. Senda, S. Nakano, H. Kunii and H. Itoh, J. Chem. Soc., Perkin Trans. 2, 1993, 1009 DOI: 10.1039/P29930001009

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