| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5216733 | Tetrahedron | 2014 | 7 Pages |
Abstract
New series of acridines and phenanthrolines have been prepared from β-chlorovinyl aldehydes and various aniline derivatives allowing the installation of valuable substituents, such as ketone, nitro or amino groups at the heterocyclic core. X-ray analyses confirmed the structures of acridines and phenanthrolines as well as the presence of partially hydrogenated rings and their crucial impact on the overall shape of the acridine-based architectures. 1H NMR revealed the helical behaviour of several acridine motives. Comparison of UV data between architectures and influence of number of partially hydrogenated rings is also described.
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Physical Sciences and Engineering
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