
doi: 10.1002/mrc.3959
pmid: 23696534
In this article, we describe the characteristic 15N and 1HN NMR chemical shifts and 1J(15N–1H) coupling constants of various symmetrically and unsymmetrically substituted 1,4‐dihydropyridine derivatives. The NMR chemical shifts and coupling constants are discussed in terms of their relationship to structural features such as character and position of the substituent in heterocycle, N‐alkyl substitution, nitrogen lone pair delocalization within the conjugated system, and steric effects. Copyright © 2013 John Wiley & Sons, Ltd.
Dihydropyridines, Magnetic Resonance Spectroscopy, Nitrogen Isotopes, Quantum Theory
Dihydropyridines, Magnetic Resonance Spectroscopy, Nitrogen Isotopes, Quantum Theory
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