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Al-Najjar, I.M. and Amin, H.B. (1987) The Carbon-13 Chemical Shifts and the Analysis of the Relaxation Times T1 and Long Range 13C-1H Coupling Constants of Quinoline and of 1-(X-Quinolyl) Ethyl Acetate Derivatives. Spectrochimica Acta Part A: Molecular Spectroscopy, 43, 1307-1315.
http://dx.doi.org/10.1016/S0584-8539(87)80002-8

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.