A naphthyridine-based receptor for sensing citric acid

Tetrahedron Letters

Volumn 48, Issue 16, 2007, Pages 2935-2938

  Ghosh, Kumaresh ^a   Sen, Tanushreee ^a   Fröhlich, Roland ^b  

^a UNIVERSITY OF KALYANI   (India)

^b UNIVERSITY OF MÜNSTER   (Germany)

Author keywords

Citric acid binding; Fluorescence sensing; Maleic acid binding; Naphthyridine; Selective recognition of carboxylic acid

Indexed keywords

CARBOXYLIC ACID DERIVATIVE; CITRIC ACID; FUMARIC ACID; MALEIC ACID; NAPHTHYRIDINE DERIVATIVE;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL BINDING; CHEMICAL STRUCTURE; CITRIC ACID CYCLE; FLUORESCENCE SPECTROSCOPY; ORGANIC CHEMISTRY; PROTON NUCLEAR MAGNETIC RESONANCE; ULTRAVIOLET SPECTROSCOPY;

EID: 33947233248     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.02.047     Document Type: Article

References (25)

1. Jadhav V.D., and Schmidtchen F.P. Org. Lett. 8 (2006) 2329
2. Gunnlaugsson T., Davis A.P., O'Brien J., and Glynn E.M. Org. Lett. 4 (2002) 2449
3. Raker J., and Glass T.E. J. Org. Chem. 67 (2002) 6113
4. Bell T.W., and Hext N.M. Chem. Soc. Rev. 33 (2004) 589
5. Ghosh K., and Masanta G. Tetrahedron Lett. 47 (2006) 2365 and references cited therein
6. Ghosh K., and Masanta G. Supramol. Chem. 17 (2005) 331
7. Ghosh K., and Masanta G. Tetrahedron Lett. 47 (2006) 9233
8. Ghosh K., and Masanta G. Chem. Lett. 34 (2006) 414
9. Ghosh K., and Adhikari S. Tetrahedron Lett. 47 (2006) 3577
10. Styrer L. Biochemistry. 3rd ed. (1988), Freeman, New York pp 188, 373-394, 575
11. Gougoux A., Lemieux G., and Lavoie N. Am. J. Physiol. 231 (1976) 1010
12. Eiamong S., Spohn M., Kurtzman N.A., and Sabatini S. Kidney Int. 48 (1995) 1542
13. Metzger A., and Anslyn E.V. Angew Chem., Int. Ed. 37 (1988) 649
14. Wiskur S.L., Ait-Haddou H., Lavigue J.L., and Anslyn E.V. Acc. Chem. Res. 34 (2001) 963
15. Fabbrizzi L., Fotti F., and Taglieti A. Org. Lett. 7 (2005) 2603
16. Parker D., and Yu J. Chem. Commun. (2005) 3141
17. Clares M.P., Lodeiro C., Fernandez D., Parola A.J., Pina F., Garcia-Espana E., Soriano C., and Tejero R. Chem. Commun. (2006) 3824 and references cited therein
18. Wiskur S.L., Ait-Haddou H., Lavigne J.J., and Anslyn E.V. Acc. Chem. Res. 34 (2001) 963
19. Corbin P.S., Zimmerman S.C., Thiessen P.A., Hawryluk N.A., and Murray T.J. J. Am. Chem. Soc. 123 (2001) 10475
20. +, 556.3, 425.2, 382.3, 362.2.
21. 2 = 0.103. CCDC No. 631313.
22. Energy minimization: MMX (PC Model Serena Software 1993) using standard constants and dielectric constant of 1.5.
23. Chou P.T., Wu G.R., Wei C.Y., Cheng C.C., Chang C.P., and Hung F.T. J. Phys. Chem. B. 104 (2000) 7818
24. Mazik M., Radunz W., and Boese R. J. Org. Chem. 69 (2004) 7448
25. Goswami S., Ghosh K., and Mukherjee R. Tetrahedron 57 (2001) 4987