Synthetic receptors for neutral nitro derivatives

Tetrahedron Letters

Volumn 50, Issue 3, 2009, Pages 359-362

  Athikomrattanakul, Umporn ^a,b   Promptmas, Chamras ^b   Katterle, Martin ^a  

^a FRAUNHOFER INSTITUTE FOR BIOMEDICAL ENGINEERING   (Germany)

^b MAHIDOL UNIVERSITY   (Thailand)

Author keywords

Arylurea based receptor; Binding constants; Guanidine based receptor; Nitro derivatives

Indexed keywords

DIMETHYL SULFOXIDE; GUANIDINE; NITRO DERIVATIVE; UREA;

ARTICLE; BINDING AFFINITY; CHEMICAL BINDING; CHEMICAL STRUCTURE; FLUORESCENCE SPECTROSCOPY; SYNTHESIS;

EID: 57149130664     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2008.11.015     Document Type: Article

References (26)

1. Schmidtchen F.P., and Berger M. Chem. Rev. 97 (1997) 1609
2. Seel C., and de Mendoza J. In: Vogtle F. (Ed). Comprehensive Supramolecular Chemistry Vol. 2 (1996), Elseiver Science
3. Fitzmaurice R.J., Kyne G.M., Douheret D., and Kilburn J.D. J. Chem. Soc., Perkin Trans. 1 (2002) 841
4. Fan E., van Arman S.A., Kincaid S., and Hamilton A.D. J. Am. Chem. Soc. 115 (1993) 369
5. Bonizzoni M., Febbrizzi L., Tagliettim A., and Tiengo F. Eur. J. Org. Chem. (2006) 3567
6. Herrera R.P., Sgarzani V., Bernardi L., and Ricci A. Angew. Chem., Int. Ed. 44 (2005) 6576
7. Okino T., Hoashi Y., Furukawa T., Xu X., and Takemoto Y. J. Am. Chem. Soc. 127 (2005) 119
8. Müller G., Riede J., and Schmidtchen F.P. Angew. Chem., Int. Ed. Engl. 27 (1988) 1516
9. Echavarren A.M., Galán A., Lehn J.M., and de Mendoza J. J. Am. Chem. Soc. 111 (1989) 4994
10. Galán A., Andreu D., Echavarren A.M., Prados P., and de Mendoza J. J. Am. Chem. Soc. 114 (1992) 1511
11. Schmidtchen F.P. Tetrahedron Lett. 30 (1989) 4493
12. Andreu C., Galán A., Kobiro K., de Mendoza J., Park T.K., Rebek J.Jr., Salmerón A., and Ussman N. J. Am. Chem. Soc. 116 (1994) 5501
13. Schiessl P., and Schmidtchen F.P. J. Org. Chem. 59 (1994) 509
14. Schmuck C. Chem. Commun. (1999) 843
15. Schmuck C. Eur. J. Org. Chem. (1999) 2397
16. Kelly T.R., and Kim M.H. J. Am. Chem. Soc. 116 (1994) 7072
17. Linton B.R., Goodman M.S., and Hamilton A.D. Chem. Eur. J. 6 (2000) 2449
18. Hall A.J., Manesiotis P., Emgenbroich M., Quagilia M., de Lorenzi E., and Sellergren B. J. Org. Chem. 70 (2005) 1732
19. Niu C.G., Yang X., Lin W.Q., Shen G.L., and Yu R.Q. Analyst 127 (2002) 512
20. Boyle P.H., Convey M.A., Davis A.P., Hosken G.D., and Murray B.A. J. Chem. Soc., Chem. Commun. (1992) 239
21. van A E., Wynberg H., and van B F. J. Chem. Soc., Chem. Commun. (1992) 629
22. Wilcox C.S., Kim E., Romano D., Kuo L.H., Burt A.L., and Curran D.P. Tetrahedron 51 (1995) 621
23. Kannan R., Harris C.M., Harris T.M., Waltho J.P., Skelton N.N., and Williams D.H. J. Am. Chem. Soc. 110 (1988) 2946
24. Cook J.L., Hunter C.A., and Low C.M.R. Angew. Chem. 119 (2007) 3780
25. Bates G.W., Triyanti M., Light E., Albrecht M., and Gale P.A. J. Org. Chem. 72 (2007) 8921
26. Βlatt E., Chatelier R.C., and Sawzer W.H. Biophys. J. 50 (1986) 349