Jump to main content
Jump to site search
Access to RSC content Close the message box

Continue to access RSC content when you are not at your institution. Follow our step-by-step guide.


Issue 12, 1995
Previous Article Next Article

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.

Back to tab navigation

Article information


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

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

Search articles by author

Spotlight

Advertisements