A rapid and efficient preparation of linear and macrocyclic polyamine bolaphiles

Synthetic Communications

Volumn 27, Issue 16, 1997, Pages 2833-2845

  Bradley, J C ^a,b   Vigneron, J P ^a   Lehn, J M ^a  

^a Centre de Recherche Interdisciplinaire en Biologie   (France)

^b DREXEL UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

MACROCYCLIC COMPOUND; POLYAMINE DERIVATIVE;

ARTICLE; COLUMN CHROMATOGRAPHY; CYCLIZATION; POLYMERIZATION; SYNTHESIS;

EID: 0030738713     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397919708004159     Document Type: Article

References (7)

1. Frugier, M.; Florentz, C.; Hosseini, M.W.; Lehn, J.-M.; Giegé, R. Nucleic Acids Research 1994, 22, 2784.
2. Oriol-Audit, C.; Hosseini, M.W.; Lehn, J.-M. Eur. J. Biochem. 1985, 151, 557.
3. Bellevue III, F.H.; Boahbedason, M.; Wu, R.; Woster, P.M., Bioorg. Med. Chem. Lett. 1996, 6, 2765 and references therein.
4. Hosseini, M.W.; Lehn, J.-M. Helv. Chim. Acta. 1986, 69, 587.
5. McManis, J.S.; Ganem, B. J. Org. Chem. 1980, 45, 2041.
6. Bergeron, R.J.; Seligsohn, H.W. Bioorg. Chem. 1986, 14, 345.
7. Acylation of the analogous protected spermidine derivatives exhibited a 3:1 preference of the primary over secondary terminal amines. See Tice, C.M.; Ganem, B. J. Org. Chem. 1983, 48, 2106.