Facile and efficient synthesis of fluoroalkyl aryl ethers

Tetrahedron Letters

Volumn 43, Issue 41, 2002, Pages 7353-7355

  Kamal, Ahmed ^a   Pratap, T B ^a   Ramana, K Venkata ^a   Ramana, A V ^a   Babu, A Hari ^a  

^a INDIAN INSTITUTE OF CHEMICAL TECHNOLOGY   (India)

Author keywords

[No Author keywords available]

Indexed keywords

ETHER; FLUORIDE; FLUORINE DERIVATIVE; OXYGEN; PHENOL;

ANALYTIC METHOD; ARTICLE; CHEMICAL BOND; CHEMICAL REACTION; COMPLEX FORMATION; DRUG SYNTHESIS; ETHERIFICATION; REACTION TIME; TEMPERATURE DEPENDENCE;

EID: 0037037993     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(02)01719-7     Document Type: Article

References (21)

1. Kirk, K. L.; Filler, R. In Biomedical Frontiers of Fluorine Chemistry; Ojima, I.; McCarthy, J. R.; Welch, J. J., Eds.; ACS Symposium Series 639; American Chemical Society: Washington, DC, 1996 Elliot, A. J. In Fluorinated Pharmaceuticals In Chemistry of Organic Fluorine Compounds II: A Critical Review; Hudlicky, M.; Pavlath, A. E., Eds.; ACS Monograph 187; American Chemical Society: Washington, DC, 1995 Lang, R. W. Fluorinated Agrochemicals. In Chemistry of Organic Fluorine Compounds II; Hudlicky, M.; Pavlath, A. E., Eds.; ACS Monograph 187; American Chemical Society: Washington, DC, 1995.
2. Smart B.E. Characteristics of C-F Systems. Banks R.E., Smart B.E., Tatlow J.C., Organofluorine Chemistry. Principles and Commercial Applications. 1994;Plenum, New York.
3. Olah A., Surya Prakash G.K., Chambers R.D. Synthetic Fluorine Chemistry. 1992;Wiley and Sons, New York.
4. Gerstenberger M.R.C., Haas A. Angew. Chem., Int. Ed. Engl. 20:1981;647-667.
5. Ramachandran, P. V. Asymmetric Fluoroorganic Chemistry, Applications, and Future Directions, ACS Symposium Series, 2000, p. 746.
6. Muniz K. Angew. Chem., Int. Ed. 40:2001;1653-1656.
7. Ernest, P. US Patent 4,870,089 (1989), Chem. Abstr. 1990, 112, 118665e Angelina, D. US Patent 4,767,779 (1988); Chem. Abstr. 1989, 111, 39359j Walter, S.; Juergen, V.; Gerd, H.; Wolfgang, S.; Heinrich, A. Ger. Offen. DE 3,213,512 (1983); Chem. Abstr. 1984, 100, 68527r.
8. Albrecht, M. Eur. Patent EP 318,781 (1989), Chem. Abstr. 1989, 111, 232286m.
9. Otto, S.; Gerhard, H.; Hubert, S. US Patent 3,937,726 (1976); Chem. Abstr, 1976, 85, 192415p Otto, S.; Gerhard, H.; Hubert, S. US Patent 4,013,452 (1977); Chem. Abstr. 1977, 87, 5675e David, C.; John, C. D. Eur. Patent. 63,873 (1981); Chem. Abstr. 1983, 98, 178977k.
10. Thomas, C.; Eugen, K. Ger. Offen. DE 3,430,513 (1986); Chem. Abstr. 1986, 105, 120482s Louis, C.; Jacques, P.; Philippe, T. Fr. Demande 2,293,472 (1976); Chem. Abstr. 1977, 86, 1415618 Louis, C.; Jacques, P.; Philippe, T. Fr. Demande 2,293,478 (1976); Chem. Abstr. 1977, 86, 1415619w.
11. Bernhard, K.; Ernst, S.; Kurt, K.; Richard, R.; Volker, F.; Georg, R.; Hartmann, S.; Jeorg, S. B. S. African ZA 8,403,288 (1984); Chem. Abstr. 1985, 103, 160504r Bernhard, K.; Ernst, S.; Kurt, K.; Richard, R.; Volker, F.; Georg, R.; Hartmann, S.; Jeorg, S. B. PCT Int. Appl. WO8, 602,645 (1986); Chem. Abstr. 1986, 105, 208884k.
12. Idoux J.P., Madenwald M.L., Garcia B.S., Chu D.L. J. Org. Chem. 50:1985;1876-1878.
13. Idoux J.P., Gupton J.T., McCurry C.K., Crews A.D., Jurss C.D., Colon C., Ramphi R.C. J. Org. Chem. 48:1983;3771-3773.
14. Suzuki H., Matuoka T., Ohtsuka I., Osuka A. Synthesis. 1985;499-500 Fabwerke Fr. Demande 2,005,876 (1969); Chem. Abstr. 1970, 73, 36584q.
15. Fabwerke Fr. Demande 2,005,876 (1969); Chem. Abstr. 1970, 73, 36584q
16. McBee E.T., Bolt R.O. Ind. Eng. Chem. 39:1947;412-415.
17. Gupton J.T., Idoux J.P., DeCrescenzo G., Colon C. Synth. Commun. 14:1984;621-629 Bakhmutov, Y. L.; Martinova, N. P.; Denisenkov, V. F.; Ilin, A. N.; Aksenov, V. S.; Minayev, S. N.; Ivanova, L. M. RU Patent 2055830 C1 (1993).
18. Bakhmutov, Y. L.; Martinova, N. P.; Denisenkov, V. F.; Ilin, A. N.; Aksenov, V. S.; Minayev, S. N.; Ivanova, L. M. RU Patent 2055830 C1 (1993).
19. Feiring A.E. J. Org. Chem. 44:1979;2907-2910.
20. Clark J.H., Owen N.D.S. Tetrahedron Lett. 28:1987;3627-3630.
21. +, 100%).