Zeolite HY and silica gel as new and efficient heterogenous catalysts for the synthesis of triarylimidazoles under microwave irradiation

Monatshefte fur Chemie

Volumn 131, Issue 9, 2000, Pages 945-948

  Balalaie, Saeed ^a   Arabanian, Armin ^a   Hashtroudi, Mehri S ^b  

^a K N TOOSI UNIVERSITY OF TECHNOLOGY   (Iran)

^b MATERIALS AND ENERGY RESEARCH CENTER   (Iran)

Author keywords

Cyclocondensation; Microwave irradiation; Silica gel; Solvent free condition; Triarylimidazole derivatives

Indexed keywords

EID: 0034389275     PISSN: 00269247     EISSN: None     Source Type: Journal    
DOI: 10.1007/s007060070049     Document Type: Article

References (31)

1. a) Satoru I (1989) Japan Kokkai Tokyo Koho JP 01, 117, 867 [89, 117, 867]; Chem Abstr 111: 214482;
2. a) Satoru I (1989) Japan Kokkai Tokyo Koho JP 01, 117, 867 [89, 117, 867]; Chem Abstr 111: 214482;
3. b) Sensui H, Ichikawa J, Sato S (1987) Japan Kokkai Tokyo Koho JP 62, 94, 841 [87, 94, 841]; Chem Abstr 107: 187436q
4. b) Sensui H, Ichikawa J, Sato S (1987) Japan Kokkai Tokyo Koho JP 62, 94, 841 [87, 94, 841]; Chem Abstr 107: 187436q
5. Liebl R, Handte R, Mildenberger H, Bauer K, Bieringer H (1987) Ger Offen DE 3, 604, 042; Chem Abstr 108: 6018g
6. Liebl R, Handte R, Mildenberger H, Bauer K, Bieringer H (1987) Ger Offen DE 3, 604, 042; Chem Abstr 108: 6018g
7. Pozherskii AF, Soldatenkov AT, Katritzky AR (1997) Heterocycles in Life and Society. Wiley, New York, pp 179-180
8. a) Lombardino JG, Wiseman EH (1974) J Med Chem 17: 1182;
9. b) Lombardino JG (1972) Ger Offen 2, 155, 558; Chem Abstr 77: 101607y
10. b) Lombardino JG (1972) Ger Offen 2, 155, 558; Chem Abstr 77: 101607y
11. Phillips AP, White HL, Rosen S (1982) Eur Pat Appl EP 58, 890; Chem Abstr 98: 53894z
12. Phillips AP, White HL, Rosen S (1982) Eur Pat Appl EP 58, 890; Chem Abstr 98: 53894z
13. a) Gilchrist TL (1992) Heterocyclic Chemistry. Longman Scientific & Technical, England, pp 74-78, 288-290;
14. b) Joule JA, Mills K, Smith GF (1995) Heterocyclic Chemistry. Chapman & Hall, London, pp 384-388;
15. c) Coffey S, Ansell MF (1986) Rodd's Chemistry of Carbon Compounds, vol IV. Elsevier, New York, pp 119-196
16. a) Davidson D, Weiss M, Jelling M (1937) J Org Chem 2: 319;
17. b) Cook AH, Jones DC (1941) J Chem Soc 278;
18. c) EC Chemical Industry Co (1985) Japan Kokkai Tokyo Koho JP 60, 55, 038 [85, 55, 038]; Chem Abstr 103: 161866x;
19. c) EC Chemical Industry Co (1985) Japan Kokkai Tokyo Koho JP 60, 55, 038 [85, 55, 038]; Chem Abstr 103: 161866x;
20. d) Zhang C, Moran EJ, Woiwode TF, Short KM, Mjalli AMM (1996) Tetrahedron Lett 37: 751;
21. e) White DM, Sonnenberg J (1964) J Org Chem 23: 1926
22. a) Abramovitch RA (1991) Org Prep Proc Int 23: 683;
23. b) Mingos DMP, Baghurst DR (1991) Chem Soc Rev 20: 1;
24. c) Caddick S (1995) Tetrahedron 51: 10403;
25. d) Strauss CR, Trainer RW (1995) Aust J Chem 48: 1665;
26. e) Loupy A, Petit A, Hamelin A, Texier-Boullet F, Jacquault P, Mathe D (1998) Synthesis 1213;
27. f) Varma RS (1999) Green Chem 1: 43
28. Balalaie S, Hashtroudi M, Sharifi A (1999) J Chem Res 329
29. a) Smith K (1992) Solid Supports and Catalysts in Organic Chemistry. Ellis Horwood, Chichester, pp 130-170;
30. b) Izumi Y, Urabe K, Onaka M (1992) Zeolite, Clay, and Heteropoly Acid in Organic Reactions. Kodansha & VCH, Tokyo, pp 1-47;
31. c) Martin-Luengo MA, Yates M (1995) Journal of Material Science 30: 4483-4491