Abstract
A novel set of dimers derived from 9-amino acridine was prepared and characterized by1H and13CNMR. These derivatives are bridged at several different positions of the heterocyclic moieties, by the way of α,ω-diamido or α,ω-diamino side-chains. Additionally the preparation of some bi-bridged compounds was achieved.
Zusammenfassung
Es wurde eine neue Reihe von Dimeren des 9-Aminoacridins hergestellt und mittels1H und13C-NMR charakterisiert. Diese Derivate sind an verschiedenen Positionen des Heterocyclus mit α,ω-Diamido- oder α,ω-Diamino-Seitenketten überbrückt. Zusätzlich wurden auch einige zweifachüberbrückte Verbindungen hergestellt.
Similar content being viewed by others
References
Le Pecq, J. B., Le Bret, M., Barbet, J., Roques, B. (1975) Proc. Nat. Acad. Sci. USA72: 2915
Chen, T. K., Fico, R., Canellakis, E. S. (1978) J. Med. Chem.21: 868
McR. Wright, R. G., Wakelin, L. P. G., Fieldes, A., Acheson, R. M., Waring, M. J. (1980) Biochem.19: 5825
Atwell, G. J., Stewart, G. M., Leupin, W., Denny, A. (1985) J. Am. Chem. Soc.107: 4335
Zimmerman, S. C., Lamberson, C. R., Cory, M., Fairley, T. A. (1989) J. Am. Chem. Soc.111: 6805
Takenaka, S., Jhara, T., Takagi, M. (1990) J. Chem. Soc., Chem. Commun. 1485
Olomucki, M., Jerram, M., Parfait, R., Bollen, A., Gros, F. (1981) Bioorg. Chem.10: 455
Galy, J. P., Vincent, E. J., Galy, A. M., Barbe, J., Elguero, J. (1981) Bull. Soc. Chim. Belges90: 947
Albert, A., Linnell, W. H. (1936) J. Chem. Soc. 1614
Wilkinson, J. H., Finar, I. L. (1946) J. Chem. Soc.115
White, E. (1973) Org. Syntheses Coll.5: 336
Vidal, R., Galy, J. P., Vincent, E. J., Barbe, J. (1988) Synthesis 148
Albert, A., Gledhill, W. (1942) J. Soc. Chem. Ind.61: 159
Buck, J. S., Ide, W. S. (1959) Org. Synthesis Coll.2: 130
Dhar, M. L., Narang, K. S., Ray, J. N. (1938) J. Chem. Soc. 104
Author information
Authors and Affiliations
Rights and permissions
About this article
Cite this article
Moisan, M., Galy, JP., Galy, AM. et al. New α,ω-diamido and α,ω-diamino mono-and bi-bridged acridine dimers. Monatsh Chem 124, 23–35 (1993). https://doi.org/10.1007/BF00808507
Received:
Accepted:
Issue Date:
DOI: https://doi.org/10.1007/BF00808507