Improved synthesis of DCDHF fluorophores with maleimide functional groups

Tetrahedron Letters

Volumn 47, Issue 40, 2006, Pages 7213-7217

  Lu, Zhikuan ^a   Weber, Ryan ^a   Twieg, Robert J ^a  

^a KENT STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINE; DICYANODIHYDROFURAN; FLUORESCENT DYE; FLUORINE DERIVATIVE; FURAN DERIVATIVE; MALEIMIDE; THIOL DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL REACTION KINETICS; DIELS ALDER REACTION; MITSUNOBU REACTION; PHOTOCHEMISTRY; PHYSICAL CHEMISTRY; SUBSTITUTION REACTION;

BETULACEAE;

EID: 33748769523     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.07.142     Document Type: Article

References (20)

1. Moerner W.E., and Orrit M. Science 283 (1999) 1670-1676
2. Weiss S. Science 283 (1999) 1676-1683
3. Kim S.Y., Semyonov A.N., Twieg R.J., Horwich A.L., Frydman J., and Moerner W.E. J. Phys. Chem. B 109 (2005) 24517-24525
4. Willets K.A., Nishimura S.Y., Schuck P.J., Twieg R.J., and Moerner W.E. Acc. Chem. Res. 38 (2005) 549-556
5. Willets K.A., Ostroverkhova O., He M., Twieg R.J., and Moerner W.E. J. Am. Chem. Soc. 125 (2003) 1174-1175
6. Nishimura S.Y., Lord S.J., Klein L.O., Willets K.A., He M., Lu Z., Twieg R.J., and Moerner W.E. J. Phys. Chem. B 110 (2006) 8151-8157
7. de Silva A.P., Gunaratne H.Q.N., and Gunnlaugsson T. Tetrahedron Lett. 39 (1998) 5077-5080
8. Zhang X., Li Z.C., Li K.B., Du F.S., and Li F.M. J. Am. Chem. Soc. 126 (2004) 12200-12201
9. Girouard S., Houle M.H., Grandbois A., Keillor J.W., and Michnick S.W. J. Am. Chem. Soc. 127 (2005) 559-566
10. Corrie J.E.T. J. Chem. Soc., Perkin Trans. 1 (1994) 2975-2982
11. Reddy P.Y., Kondo S., Fujita S., and Toru T. Synthesis (1998) 999-1002
12. Clevenger R.C., and Turnbull K.D. Synth. Commun. 30 (2000) 1379-1388
13. Walker M.A. J. Org. Chem. 60 (1995) 5352-5355
14. Farha O.K., Julius R.L., and Hawthorne M.F. Tetrahedron Lett. 47 (2006) 2619-2622
15. He M., Twieg R.J., Ostroverkhova O., Gubler U., Wright D., and Moerner W.E. Proc. SPIE 4802 (2002) 9-20
16. 3Na, 520.2325; found, 520.2332.
17. Kwart H., and Burchuk I. J. Am. Chem. Soc. 74 (1952) 3094-3097
18. 3) 8.85 (s, br, 1H), 6.51 (dd, J = 1.5, 5.5 Hz, 1H), 6.31 (d, J = 5.7 Hz, 1H), 5.24 (d, J = 1.5 Hz, 1H), 3.02 (ddd, J = 6.4 Hz, 1H), 2.76 (d, J = 6.4 Hz, 1H), 1.75 (s, 3H).
19. Hughes D.L. Org. React. 42 (1992) 335-656
20. 3) δ 8.35 (d, J = 2.1 Hz, 1H), 7.88 (dd, J = 9.1, 2.1 Hz, 1H), 7.82 (d, J = 9.3 Hz, 1H), 7.72 (d, J = 9.1 Hz, 1H), 7.22 (dd, J = 9.2, 2.5 Hz, 1H), 7.00 (d, J = 2.5 Hz, 1H), 6.70 (s, 2H), 3.82 (t, J = 6.6 Hz, 2H), 3.69 (t, J = 7.6 Hz, 2H), 3.46 (t, J = 7.6 Hz, 2H), 1.94 (s, 6H), 1.72-1.65 (m, 2H), 1.43-1.30 (m, 6H), 0.94 (t, J = 7.0 Hz, 3H)...