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Electrostatic vs. orbital effects as stereoinductive factors in nucleophilic additions to the endo-substituted norbornan-7-one ring system
G. Mehta, , W. Adcock
Published in
1995
   
Issue: 12
Pages: 2189 - 2190
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.
About the journal
JournalJournal of the Chemical Society, Perkin Transactions 2
ISSN1472779X