The complete 13C NMR analysis of 3‐substituted camphors with F, Cl, Br, I, OH, OMe, SMe, NHMe, NMe2 and Me substituents at endo and exo positions, and also the corresponding ‘oxo’ and dichloro derivatives, were obtained by 1D and 2D NMR techniques. The resulting substituent‐induced chemical shifts (SCS) for these difunctional systems show the influence of electronic and steric mechanisms.
No takes yet. Share an insight, caveat, or question.
Kaiser et al. (2001) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: