3-(4-acyl-3-hydroxyphenyl)-1,2-dioxetanes as a chemiluminescent substrate with high efficiency in an aqueous system

Tetrahedron Letters

Volumn 37, Issue 47, 1996, Pages 8535-8538

  Matsumoto, Masakatsu ^b   Arai, Nobuyuki ^a   Watanabe, Nobuko ^a  

^a KANAGAWA UNIVERSITY   (Japan)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

1,2 DIOXETANE DERIVATIVE;

ARTICLE; CHEMOLUMINESCENCE;

EID: 0347206903     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/0040-4039(96)01985-5     Document Type: Article

References (16)

1. 1. Schaap, A. P.; Gagnon, S. D. J. Amer. Chem. Soc. 1982, 104, 3504-3506.
2. 2. Schuster, G. B.; Acc. Chem. Res. 1979, 12, 366-373. See also Catalani, L. H.; Wilson, T. J. Amer. Chem. Soc. 1989, 111, 2633-2639.
3. 2. Schuster, G. B.; Acc. Chem. Res. 1979, 12, 366-373. See also Catalani, L. H.; Wilson, T. J. Amer. Chem. Soc. 1989, 111, 2633-2639.
4. 3. Schaap, A. P.; Chen, T.-S.; Handley, R. S.; DeSilva, R.; Giri, B. P. Tetrahedron Lett., 1987, 28, 1155-1158.
5. 4. Beck, S.; Köster, H. Anal. Chem. 1990, 62, 2258-2270.
6. 5. a) Bronstein, I.; Voyta, J. C.; Thorpe, G. H. G.; Kricka, L. J.; Armstrong, G. Clin. Chem. 1989, 35, 1441-1446;
7. b) Thorpe, G. H. G.; Bronstein, I.; Kricka, L. J.; Edwards, B.; Voyta, J. C.; Clin. Chem. 1989, 35, 2319-2321;
8. See also a) Bronstein, I.; Voyta, J. C.; Edwards, B. Anal. Biochem. 1989, 180, 95-98;
9. b) Bronstein, I.; Fortin, J.; Stanley, P. E.; Stewart, G. S. A. B.; Kricka, L. J.Anal. Biochem. 1994, 219, 169-181;
10. c) Bronstein, I.; Olesen, C. E. M. Detection Methods Using Chemiluminescence In Molecular Methods for Virus Detection; Wiedbrauk, D. L.; Farkas, D. H. Ed.; Academic, NY, 1995, pp149-173.
11. 6. Schaap, A. P.; Akhavan, H.; Romano, L. J.; Clin. Chem. 1989, 35, 1863-1864.
12. -1; Mass (m/z, %) 344 (M+, trace), 312 (24), 278 (4), 194 (60), and 179 (100).
13. 8. Matsumoto, M.; Suganuma, H.; Katao, Y.; Mutoh, H. J. Chem. Soc. Chem. Commun. 1995, 431 -432.
14. 9. Relative quantum yield based on the value for la (ref. 3).
15. 10. Further experiments are required to discuss these tendencies in detail, though they were not observed for 1d.
16. 11. The CsOH system was chosen as a representative because it induced the shortest half-life emission of 4a.