Y. Tanoue et al., POSITIONAL ASSIGNMENTS OF A SUBSTITUENT GROUP OF 3-SUBSTITUTED JUGLONES BY THE OFF-RESONANCE C-13 NMR-SPECTRA, Bulletin of the Chemical Society of Japan, 67(10), 1994, pp. 2886-2887
Taking into account the fact that the long-range C-13-H-1 coupling con
stant 3J(CH) is greater than 2J(CH), positional assignments of a subst
ituent group of 3-substituted juglones were easily accomplished by off
-resonance C-13 NMR spectra using a 60-MHz instrument for H-1. This me
thod was applicable to a structural determination of naphthazarin deri
vatives.