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1H NMR study of heterocyclic symmetric and asymmetric Tröger's base analogs containing the acridine ring

✍ Scribed by M. Demeunynck; C. Fontaine; J. Lhomme


Publisher
John Wiley and Sons
Year
1999
Tongue
English
Weight
170 KB
Volume
37
Category
Article
ISSN
0749-1581

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✦ Synopsis


The 1H NMR spectra of a series of acridine-derived Tro gerÏs base analogs substituted at various positions were registered. Also the 1H NMR characteristics of the Ðrst heterocyclic asymmetric Tro gerÏs base analog constituted of one acridine and one phenanthroline nucleus with the two corresponding symmetric Tro gerÏs bases were compared. The analysis of the NMR data clearly shows that the chemical shifts of endo/exo protons of heterocyclic Tro gerÏs base analogs are strongly dependant on the nature and geometry of the constituting heterocycles.


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