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Pyridoacridine, Quinoacridine, and Related Alkaloids

There has been considerable interest in pyridoacridines and related compounds owing to their biological activity (cytotoxicity, mutagenicity, or antibacterial activity). Wawer and coworkers [127] reported the study of a pair of quinoacridinium salts from this [Pg.460]

Copp and coworkers [128] reported the isolation of two new pyridoacridine analogs, isodiplamine (169) and lissoclinidine (170) from the New Zealand ascidian Lissodinum notti. The authors used 6 Hz optimized HMBC data in the [Pg.464]

Alkaloids are widely distributed in both terrestrial and marine organisms. The feasibility of performing direct and long-range heteronuclear shift correla- [Pg.465]

We have also attempted to highlight the value of N chemical shift calculations for establishing Fj spectral windows when performing long-range heteronuc- [Pg.465]

Finally, there are several very interesting papers currently in press. First, work by Rupee and Freeman [129] has demonstrated the possibility of obtaining natural abundance correlation spectra using vitamin B-12 as a model compound for [Pg.465]

During the period covered by this review, from 2007 through April 2014, there were no reports that we are aware of that utilized NMR data in [Pg.63]


Pyridoacridine, Quinoacridine, and Related Alkaloids 461 Tab. 14.9 Che mical shifts of tetrahydrodiazepinopurine analogs of asmarine-A (148) [124],... [Pg.461]


See other pages where Pyridoacridine, Quinoacridine, and Related Alkaloids is mentioned: [Pg.460]    [Pg.463]    [Pg.63]    [Pg.460]    [Pg.463]    [Pg.63]   


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Alkaloids quinoacridine

Pyridoacridine

Pyridoacridine alkaloids

Pyridoacridines

Quinoacridine

Related Alkaloids

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