Potential supramolecular cyclodextrin dimers using nucleobase Pairs

Synlett

Volumn , Issue 17, 2009, Pages 2875-2879

  Hamon, Florian ^a   Violeau, Bruno ^a   Turpin, Frédéric ^b   Bellot, Mathilde ^c   Bouteiller, Laurent ^c   Djedaini Pilard, Florence ^d   Len, Christophe ^a  

^a UNIVERSITÉ DE POITIERS   (France)

^b BioCydex   (France)

^c SORBONNE UNIVERSITÉ   (France)

^d UNIVERSITÉ DE PICARDIE JULES VERNE   (France)

Author keywords

Click chemistry; Cyclodextrin; Nucleobase

Indexed keywords

ADAMANTANE DERIVATIVE; ADENINE DERIVATIVE; CYCLODEXTRIN DERIVATIVE; DIMER; NUCLEIC ACID BASE; THYMINE DERIVATIVE;

ARTICLE; CHEMICAL STRUCTURE; NUCLEAR MAGNETIC RESONANCE; SILYLATION; SYNTHESIS;

EID: 70449382866     PISSN: 09365214     EISSN: 14372096     Source Type: Journal    
DOI: 10.1055/s-0029-1217988     Document Type: Article

References (31)

1. Klein S, Zoeller T, Pharmazeutische Zeitung 2008 153 24
2. Perly B, Moutard S, Djedaini-Pilard F, PharmaChem 2005 4 4
3. Li J, Xiao H, Li J, Zhong Y P., Int. J. Pharm. 2004 278 329
4. Bhushan R, Kumar R, J. Chromatogr., A 2002 62 2667
5. Mauri-Aucejo A, Llobat-Estelles M, Escarti-Carrasco M, Marin-Saez R, Anal.
6. Yakahisa E, Engel K H., J. Chromatogr., A 2005 1076 148
7. Breslow R, Dong A D., Chem. Rev. 1998 98 1997
8. Kataky R, Mogan E, Biosens. Bioelectron. 2003 18 1407
9. Surpateanu G, Becuwe M, Lungu N C., Dron P, Fourmentin S, Landy D, Surpateanu G, J.
10. Ueno A, Ikeda H, Mol. Supramol. Photochem. 2001 8 461
11. Bjerre J, Fenger T H., Marinescu L G., Bols M, Eur. J. Org.
12. Blach P, Landy D, Fourmentin S, Surpateanu G, Bricout H, Ponchel A, Hapiot F, Monflier E, Adv. Synth. Catal. 2005 347 1301
13. Huskens J, Deij M A., Reinhould D N., Angew. Chem. Int. Ed. 2002 41 4467
14. Hamada F, Kondo Y, Ishikawa K, Ittto H, Suzuki I, Osa T, Ueno A, J. Inclusion
15. Aime S, Gianolio E, Arena F, Barge A, Martina K, Heropoulos G, Cravotto G, Org. Biomol. Chem. 2009 7 370, Sliwa W, Girek T, Koziol J J., Curr.
16. Zhang B, Breslow R, J.
17. Liu Y, Zhang Q, Chen Y, J. Phys. Chem.
18. Nagai K, Kondo H, Tsuruzoe N, Hayakawa K, Kanematsu K, Heterocycles 1982 19 53
19. Nagai K, Hayakawa K, Kanematsu K, J.
20. Nagai K, Hayakawa K, Ukai S, Kanematsu K, J. Org. Chem. 1986 51 3931
21. Djedaini-Pilard F, Perly B, Dupas S, Miocque M, Galons H, Tetrahedron
22. Kato Y, Nishizawa S, Teramae N, Org.
23. Murray P E., McNally V A., Lockyer S D., Williams [nl]K J., Stratford I J., Jaffar M, Freeman S, Bioorg. Med. Chem. 2002 10 525
24. Nawrot B, Michalak O, Olejniczak S, Wieczorek [nl]M W., Lis T, Stec W J., Tetrahedron 2001 57 3979
25. Ciapetti P, Taddeai M, Tetrahedron 1998 54 11305
26. Lock L, Pohlsgaard J, Jepsen A S., Hansen L H., Nielsen H, Steffansen S I., Sparving L, Nielsen A B., Vester B, Nielsen P, J. Med. Chem. 2008 51 4957
27. Lindsell W E., Murray C, Preston P N., Woodman T A. J., Tetrahedron 2000 56 1233
28. Sartorius J, Schneider H.-J, Chem. Eur. J. 1996 2 1446
29. Salas M, Gordillo B, Gonzalez F J., ARKIVOC 2003 (xi) 72
30. Carrazana J, Jover A, Meijide F, Soto V H., Tato J V., J.
31. Tellini V H. S., Jover A, Garca J C., Galantini L, Meijide F, Tato J V., J.