Issue 12, 1995

Electrostatic vs. orbital effects as stereoinductive factors in nucleophilic additions to the endo-substituted norbornan-7-one ring system

Abstract

Polar-field susceptibility parameters as well as a 13C NMR probe based on the transmission of polar substituent effects in endo-norbornan-7-ones points to the involvement of electrostatic effects in determining π-face selectivities during nucleophilic additions to this ring system.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1995, 2189-2190

Electrostatic vs. orbital effects as stereoinductive factors in nucleophilic additions to the endo-substituted norbornan-7-one ring system

G. Mehta, F. A. Khana and W. Adcock, J. Chem. Soc., Perkin Trans. 2, 1995, 2189 DOI: 10.1039/P29950002189

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