Cesium fluoride-Celite: A solid base for efficient syntheses of aromatic esters and ethers

Tetrahedron

Volumn 61, Issue 27, 2005, Pages 6652-6656

  Shah, Syed Tasadaque Ali ^a   Khan, Khalid Mohammed ^b   Hussain, Hidayat ^b   Anwar, Muhammad Usman ^a   Fecker, Miriam ^a   Voelter, Wolfgang ^a  

^a UNIVERSITY OF TÜBINGEN   (Germany)

^b UNIVERSITY OF KARACHI   (Pakistan)

Author keywords

Alcohols; Cesium fluoride Celite; Esters; Ethers

Indexed keywords

ACETONITRILE; CESIUM; CESIUM FLUORIDE; ESTER DERIVATIVE; ETHER DERIVATIVE; HALIDE; INFUSORIAL EARTH; PHENOL DERIVATIVE; REAGENT; UNCLASSIFIED DRUG;

ARTICLE; PRIORITY JOURNAL; SOLID;

EID: 20444504766     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2005.03.126     Document Type: Article

References (38)

1. T.W. Greene, and P.G.M. Wuts Protective Groups in Organic Synthesis 1991 Wiley-Interscience New York and numerous references quoted therein
2. J.C. Lee, and Y. Choi Synth. Commun. 28 1998 2021 2026
3. K.M. Khan, S. Hayat, Zia-Ullah, Atta-ur-Rahman, M.I. Choudhary, G.M. Maharvi, and E. Bayer Synth. Commun. 33 2003 3435 3453
4. S. Hayat, Atta-ur-Rahman, M.I. Choudhary, K.M. Khan, W. Schumann, and E. Bayer Tetrahedron 57 2001 9951 9957
5. V. Polshettiwar, and M.P. Kaushik Catal. Commun. 5 2004 515 518
6. K. Kitaori, Y. Furukawa, H. Yoshimoto, and J. Otera Adv. Synth. Catal. 343 2001 95 101
7. J.H. Clark, H.L. Holland, and J.M. Miller Tetrahedron Lett. 38 1976 3361 3364
8. J.H. Clark, and J.M. Miller Tetrahedron Lett. 7 1977 599 602
9. J.H. Clark, and J.M. Miller J. Am. Chem. Soc. 99 1977 498 504
10. J.H. Clark, and J.M. Miller J. Chem. Soc., Chem. Commun. 1976 229 230
11. J.H. Clark, and J.M. Miller J. Chem. Soc., Perkin Trans. 1 1977 2063 2069
12. J.H. Clark, and J.M. Miller J. Chem. Soc., Chem. Commun. 1977 64 65
13. J.M. Miller, K.-H. So, and J.H. Clark J. Chem. Soc., Chem. Commun. 1978 466 467
14. J.H. Clark J. Chem. Soc., Chem. Commun. 1978 789 791
15. T. Ooi, H. Sugimoto, K. Doda, and K. Maruoka Tetrahedron Lett. 42 2001 9245 9248
16. M. Yamada, S. Yahiro, T. Yamano, Y. Nakatani, and G. Ourisson Bull. Soc. Chim. Fr. 127 1990 824 829
17. W.H. Kruizinga, and R.M. Kollogg J. Am. Chem. Soc. 103 1981 5183 5189
18. S.T.A. Shah, K.M. Khan, M. Fecker, M.I. Choudhary, and W. Voelter Tetrahedron Lett. 43 2002 8603 8605
19. S.T.A. Shah, K.M. Khan, M. Fecker, and W. Voelter Tetrahedron Lett. 44 2003 6789 6791
20. P.B.D. de la Mare, N.S. Isaacs, and M.J. McGlone J. Chem. Soc., Perkin Trans. 2 1976 784 786
21. C.K. Lee, J.S. Yu, and H.-J. Lee J. Heterocycl. Chem. 39 2002 1207 1217
22. F.M. Menger, and J.H. Smith J. Am. Chem. Soc. 94 1972 3824 3829
23. K. Williams, and B. Halpern Synthesis 1974 727 728
24. D.S. Tarbell, and J.A. Price J. Org. Chem. 22 1957 245 250
25. British Petroleum Co. Ltd, Fr 1410774, 1965; Chem. Abstr. 1965, 63, 17909c.
26. Y. Yukawa, M. Sakai, and S. Suzuki Yuki Gosei Kagaku Kyokai Shi 24 1966 66 68
27. Chem. Abstr. 64 1966 8057g 8059a
28. E. Baciocchi, A. Piermattei, C. Rol, R. Ruzziconi, and G.V. Sebastiani Tetrahedron 45 1989 7049 7062
29. H.C. Brown, and O.J. Cope J. Am. Chem. Soc. 86 1964 1801 1807
30. P. Maslak, and R.D. Guthrie J. Am. Chem. Soc. 108 1986 2628 2636
31. R.L. Huang, H.H. Lee, and M.S. Malhotra J. Chem. Soc., Suppl. 1964 5947 5951
32. E. Taskinen J. Chem. Soc., Perkin Trans. 2 2001 1824 1834
33. K. Raman, H.K. Singh, S.K. Salzman, and S.S. Parmar J. Pharm. Sci. 82 1993 167 169
34. J.A. Lyman, and E.E. Reid J. Am. Chem. Soc. 42 1920 615 619
35. M.B. Sassaman, K.D. Kotian, G.K.S. Prakash, and G.A. Olah J. Org. Chem. 52 1987 4314 4319
36. K. Ikenaga, K. Hiramatsu, N. Nasaka, and S. Matsumoto J. Org. Chem. 58 1993 5045 5047
37. Shell Internationale Research Maatschappij N. V. Belg. 615,700, 1962; Chem. Abstr. 1963, 59, 2721e.
38. E. Hayashi, H. Yamanaka, and K. Shimizu Chem. Pharm. Bull. 7 1959 146 148