Superacidic trifluoromethanesulfonic acid-induced cycli-acyalkylation of aromatics

Catalysis Letters

Volumn 87, Issue 3-4, 2003, Pages 109-112

  Surya Prakash, G K ^a   Yan, Ping ^a   Török, Béla ^a,b   Olah, George A ^a  

^a UNIVERSITY OF SOUTHERN CALIFORNIA   (United States)

^b MICHIGAN TECHNOLOGICAL UNIVERSITY   (United States)

Author keywords

Friedel Crafts cycli acyalkylation; Indanone; Superelectrophilic activation; Tetralone; Trifluoromethanesulfonic acid

Indexed keywords

AROMATIC COMPOUNDS; CARBOXYLIC ACIDS; CHEMICAL BONDS; FRIEDEL-CRAFTS REACTION; GAS CHROMATOGRAPHY; MASS SPECTROMETRY; NUCLEAR MAGNETIC RESONANCE SPECTROSCOPY; SYNTHESIS (CHEMICAL);

SUPERELECTROPHILIC ACTIVATION;

METHANE;

EID: 0141883006     PISSN: 1011372X     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1023482904174     Document Type: Article

References (22)

1. (a) H. Heaney, in: Comprehensive Organic Synthesis, Vol. 2, eds. B.M. Trost and I. Fleming (Pergamon, Oxford, 1991) pp. 733, 753.
2. (b) G.A. Olah, R. Drishnamurti, and G.K.S. Prakash, in: Comprehensive Organic Synthesis, Vol. 1, eds. B.M. Trost and I. Fleming (Pergamon, Oxford, 1991) p. 293.
3. (c) N. Yonezawa, T. Hino and T. Ikeda, Recent Res. Dev. Synth. Org. Chem. 1 (1998) 213.
4. (d) G.A. Olah (ed.), Friedel-Crafts and Related Reaction (Wiley-Interscience, New York, 1963-65).
5. (a) H. Kusama, Y. Yamashita and K. Narasaka, Chem. Lett. (1995) 5; S. Hanessian, M. Mauduit, E. Demont and C. Talbot, Tetrahedron 58 (2002) 1485.
6. (a) H. Kusama, Y. Yamashita and K. Narasaka, Chem. Lett. (1995) 5; S. Hanessian, M. Mauduit, E. Demont and C. Talbot, Tetrahedron 58 (2002) 1485.
7. (b) M. Tiecco, L. Testaferri and M. Tingoli, Tetrahedron Lett. 49 (1993) 5351.
8. (c) D.A. Klumpp, D.N. Baek, G.K.S. Prakash and G.A. Olah, J. Org. Chem. 62 (1997) 6666.
9. (d) A. Molnár, B. Török, I. Bucsi and A. Földvári, Topics Catal. 6 (1998) 9.
10. (a) R.T. Hart and R.F. Tebbe, J. Am. Chem. Soc. 72 (1950) 3286.
11. (b) C.F. Koelsch, H. Hochmann and C.D. Le Claire, J. Am Chem. Soc. 65 (1943) 59.
12. (c) M.F. Ansell and G.F. Whitfield, Tetrahedron Lett. 26 (1968) 3075.
13. (d) J.M. Allen, K.M. Johnston, J.F. Jones, and R.G. Shooter, Tetrahedron 33 (1977) 2083.
14. (a) W.M. Welch, A.R. Kraska, R. Sarges, and B.K. Kow, J. Med. Chem. 27 (1984) 1508.
15. (b) R.A. Stalker, T.E. Munsch, J.D. Tran, X. Nie, R. Warmuth, A. Beatty and C.B. Aakeroy, Tetrahedron 58 (2002) 4837.
16. (c) K. Koehler, M. Gillner, Y. Liu, A. Cheng, J.V. Heck, M.L. Hammond, R.T. Mosley and M. Rahimi-Ghadim, PCT Int. Appl. WO 0246134, 2002.
17. (a) R.H. Woudenberg, PCT Int. Appl. WO 0236537, 2002; Chem. Abstr. 136 (2002) 369521.
18. (a) R.H. Woudenberg, PCT Int. Appl. WO 0236537, 2002; Chem. Abstr. 136 (2002) 369521.
19. (b) H. Mori and T. Hachiya, Jpn. Kokai Tokkyo Koho JP 2001247505, 2001; Chem. Abstr. 135 (2001) 242011.
20. (b) H. Mori and T. Hachiya, Jpn. Kokai Tokkyo Koho JP 2001247505, 2001; Chem. Abstr. 135 (2001) 242011.
21. (a) D.A. Klumpp, Recent Res. Dev. Org. Chem. 5 (2001) 193.
22. (b) G.A. Olah, Angew. Chem., Int. Ed. Engl. 32 (1993) 767.