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Arrosmith, J.E., Cook, M.J., Cook, D.J. and Hardsone, D.J. (1978) Long-Range Substituent Induced Chemical Shifts in 13C NMR Spectra of n-Benzylidene Benzyl Amines. Organic Magnetic Resonance, 11, 160-161.
http://dx.doi.org/10.1002/mrc.1270110314

has been cited by the following article:

• TITLE: Synthesis of Some New Pyridine-2-yl-Benzylidene-Imines

  AUTHORS: Abdulhamid Alsaygh, Jehan Al-Humaidi, Ibrahim Al-Najjar

  KEYWORDS: Schiff’s Bases, 1H, 13C-NMR, Pyridine-2-yl-Benzylidene, E-Z-Isomers, Azomethane Group

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.4 No.2, May 26, 2014

  ABSTRACT: A series of new Schiff bases derived from 2-aminopyridenes and various aromatic aldehydes have been synthesized and thoroughly investigated by 1H and 13C NMR spectroscopy. The imines were found to exist as only a single E-isomer at ambient temperature. Interestingly, 1H- and 13C-NMR chemical shifts of the (CH=N) amino group are affected by the type of substituent group (X) on the aryl ring. Furthermore UV and IR Spectra of some of the title compounds are also reported.