Nitrogen heterocycles mass spectra

In Table IV some physical data and spectral characteristics of 6,7-secoberbines are listed. Only methyl corydalate (55) is optically active. Formula 55 presents the spatial structure of this compound, deduced by Nonaka et al. (65) and confirmed by Cushman et al. by both correlation with (+)-mesotetrahydrocorysamine (72) (<5S) and total synthesis (69). It is difficult to find common characteristic features in both the mass and H-NMR spectra of these alkaloids because they differ significantly from each other in their structures. On one hand, corydalic acid methyl ester (55) incorporates a saturated nitrogen heterocycle, while the three aromatic bases (56-58) differ in the character of the side chain nitrogen. For example, in mass fragmentation, ions of the following structures may be ascribed to the most intensive bands in the spectrum of 55 ... 

The IR, NMR, and mass spectra of daphmacrine (18) suggest that it has a nitrogen heterocyclic skeleton similar to that of daphniphylline (1) but differs in the oxygen-containing moiety. The IR spectrum of this alkaloid showed two carbonyl bands at 1770 and 1730 cm-1 resulting from a five-membered lactone and an ester group, respectively. The NMR spectrum showed the presence of two tertiary methyl... 

Mass spectral data have frequently been used in the structural determination of boron heterocycles. One paper has been devoted to the mass spectra of some six-membered boron-nitrogen systems. It was concluded that the spectra could be interpreted analogously to their hydrocarbon counterparts. In all cases the molecular peak was the base peak of the spectrum (68T6755). Doubly charged molecular ions, a feature typical of aromatic compounds, are often encountered. It should be noted, however, that some certainly non-aromatic aminoboranes give such doubly charged ions as well. 

---