Beilstein J. Org. Chem.2015,11, 1667–1699, doi:10.3762/bjoc.11.183
are also discussed. Pyridoacridines were found to have a large spectrum of bioactivity and this review highlights and compares the pharmacophores that are responsible for the observed bioactivity.
Keywords: biosynthesis; 13C NMR shifts; pharmacophores; pyridoacridines; synthesis; Introduction
In
atoms. Fortunately, NMR techniques such as 1,n-ADEQUATE can be used to solve the problem of carbon assignment but the experimental time is long, the sensitivity is poor, and a substantial amount of sample is required. However, pyridoacridines present some structural features that can be used for
composition leading to the deduction of the structure.
Mass fragmentation
The mass spectrometry spectrum of pyridoacridines contains very little information due to the lack of fragments. Independent of the ionization source used to determine the elemental composition (ESI, DIC, APCI, FAB, or EI), molecules
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Graphical Abstract
Figure 1:
Fragments produced by the FAB–MS of dehydrokuanoniamine B (20) [42].