A new sulfonamide derivative as magnesium ion receptor: N-tosyl-2,6-diisopropyl-4-(2,3-dimethoxylbenzoylamide)aniline

Tetrahedron Letters

Volumn 50, Issue 16, 2009, Pages 1820-1824

  Long, Zerong ^a,b   Yang, Peiju ^a   Xia, Yana ^a,b   Yang, Zaiwen ^a,b   Wu, Biao ^a  

^a LANZHOU INSTITUTE OF CHEMICAL PHYSICS   (China)

^b UNIVERSITY OF CHINESE ACADEMY OF SCIENCES   (China)

Author keywords

Magnesium; Metal ion binding; N Tosyl 2,6 diisopropyl 4 (2,3 dimethoxylbenzoylamide)aniline; Sulfonamide

Indexed keywords

ANILINE DERIVATIVE; CALCIUM ION; CHLORIDE; IONOPHORE; MAGNESIUM ION; METHANOL; N TOSYL 2,4 DIISOPROPYL 4 (2,3 DIMETHOXYBENZOYLAMIDE)ANILINE; OXYGEN; POTASSIUM ION; PROTON; RECEPTOR; SODIUM ION; SULFONAMIDE; UNCLASSIFIED DRUG; WATER;

ABSORPTION; ARTICLE; CHEMICAL BINDING; CHEMICAL INTERACTION; CHEMICAL REACTION; CHEMICAL STRUCTURE; COMPLEX FORMATION; ELECTRON; ELECTROSPRAY MASS SPECTROMETRY; HYDROGEN BOND; INFRARED SPECTROSCOPY; MAGNETISM; MOLECULAR STABILITY; PROTON NUCLEAR MAGNETIC RESONANCE; STOICHIOMETRY; SYNTHESIS; ULTRAVIOLET SPECTROSCOPY;

EID: 61349164885     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2009.02.005     Document Type: Article

References (27)

1. Schlingmann K.P., and Gudermann T. J. Physiol. 566 (2005) 301-308
2. Goytain A., and Quamme G.A. BMC Genomics 6 (2005) 48-66
3. Jiang Y., Lee A., Chen J., Ruta V., Cadene M., Chait B.T., and Backinnon R. Nature 423 (2003) 33-41
4. Hu L., Li Z.-r., Li Y., Qu J., Ling Y.-H., Jiang J.-d., and Boykin D.W. J. Med. Chem. 49 (2006) 6273-6282
5. Li H., Bu Y., Yan S., Li P., and Cukier R. J. Phys. Chem. B 110 (2006) 11005-11013
6. Navia M.A. Science 288 (2000) 2132-2133
7. Otto H.-H., and Schirmeister T. Chem. Rev. 97 (1997) 133-171
8. Scozzafava A., Owa T., Mastrolorenzo A., and Supuran C.T. Curr. Med. Chem. 10 (2003) 925-953
9. Casini A., Scozzafava A., Mastrolorenzo A., and Supuran C.T. Curr. Cancer Drug Targets 2 (2002) 55-75
10. Clapp L.A., Siddons C.J., VanDerveer D.G., Reibenspies J.H., Jones S.B., and Hancock R.D. Dalton Trans. (2006) 2001-2007
11. Maton L., Taziaux D., Soumillion J.-P., and Jiwan J.-L.H. J. Mater. Chem. 15 (2005) 2928-2937
12. Kim J., Morozumi T., and Nakamura H. Org. Lett. 9 (2007) 4419-4422
13. Liu Y., Han M., Zhang H.-Y., Yang L.-X., and Jiang W. Org. Lett. 10 (2008) 2873-2876
14. Clapp L.A., Siddons C.J., Whitehead J.R., VanDerveer D., Rogers R., Griffin S., Jones S.B., and Hancock R. Inorg. Chem. 44 (2005) 8495-8502
15. Carver F., Hunter C.A., Livingstone D.J., McCabe J.F., and Seward E.M. Chem. Eur. J. 8 (2002) 2847-2859
16. Sharma S.K., Miller M.J., and Payne S.M. J. Med. Chem. 32 (1989) 357-367
17. Hou Z., Whisenhunt Jr. D.W., Xu J., and Raymond K.N. J. Am. Chem. Soc. 116 (1994) 840-846
18. Xu J., Durbin P.W., Kullgren B., Ebbe S.N., Uhlir L.C., and Raymond K.N. J. Med. Chem. 45 (2002) 3963-3971
19. 13C NMR, IR).
20. 2 = 0.1259 [I > 2σ(I)].
21. Chapman L., Kane M., Lassila J.D., Loeschen R.L., and Wright H.E. J. Am. Chem. Soc. 91 (1969) 6856-6858
22. Hanna R. J. Am. Ceram. Soc. 48 (1965) 376-380
23. Khalil S.K.H., and Azooz M.A. J. Appl. Sci. Res. 3 (2007) 387-391
24. Lu X.-X., Qin S.-Y., Zhou Z.-Y., and Yam V.W.-W. Inorg. Chim. Acta 346 (2003) 49-56
25. Bourson J., Pouget J., and Valeur B. J. Phys. Chem. 97 (1993) 4552-4557
26. Kuzmič P. Anal. Biochem. 237 (1996) 260-273
27. Jeon S.-J., Li H., García C., LaRochelle L.K., and Walsh P. J. Org. Chem. 70 (2005) 448-455