Facile one-pot synthesis of polysubstituted quinolines under solvent-free conditions using sulfamic acid as a reusable catalyst

Monatshefte fur Chemie

Volumn 143, Issue 3, 2012, Pages 471-478

  Zhang, Min ^a   Xiong, Biao ^a   Yang, Wei ^a   Kumar, D N T ^a   Ding, Yu Qiang ^a  

^a JIANGNAN UNIVERSITY   (China)

Author keywords

Eliminations and oxidations; Heterocylces; Multicomponent reaction; Reusable sulfamic acid catalyst; Solvent free conditions

Indexed keywords

EID: 84857526448     PISSN: 00269247     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00706-011-0590-7     Document Type: Article

References (33)

1. Roberts L, Egan TJ, Joiner KA, Hoppe HC (2008) Antimicrob Agent Chemother 52:1840
2. Vieira NC, Herrenknecht C, Vacus J, Fournet A, Bories C, Figadere B, Espindola LS, Loiseau PM (2008) Biomed Pharmacother 62:684
3. Chen YL, Fang KC, Sheu JY, Hsu SL, Tzeng CC (2001) J Med Chem 44:2374
4. Dube D, Blouin M, Brideau C, Chan CC, Desmarais S, Ethier D, Falgueyret JP, Friesen RW, Girard M, Girard Y, Guay J, Riendeau D, Tagari P, Young RN (1998) Bioorg Med Chem Lett 8:1255
5. Roma G, Braccio MD, Grossi G, Mattioli F, Ghia M (2000) Eur J Med Chem 35:1021
6. Ebisu H, Nishikawa M, Tanaka M, Okazoe T, Morizawa Y, Shinyama H, Nakamura N (1999) J Cardiovasc Pharmacol 34:526
7. Maguire MP, Sheets KR, Mcvety K, Spada AP, Zilberstein A (1994) J Med Chem 37:2129
8. Altenbach RJ, Liu H, Banfor PN, Browman KE, Fox GB, Fryer RM, Komater VA, Krueger KM, Marsh K, Miller TR, Pan J, Pan L, Sun M, Thiffault C, Wetter J, Zhao C, Zhou D, Esbenshade TA, Hancock AA, Cowart MD (2007) J Med Chem 50:5439
9. Frotscher M, Ziegler E, Marchais-Oberwinkler S, Kruchten P, Neugebauer A, Fetzer L, Scherer C, Müller-Vieira U, Messinger J, Thole H, Hartmann RW (2008) J Med Chem 51:2158
10. Zhang X, Jenekhe SA (2000) Macromolecules 33:2069
11. Jenekhe SA, Lu L, Alam MM (2001) Macromolecules 34:7315
12. Espinosa LM, Ronda JC, Galia M, Cadiz V (2010) J Polym Sci Polym Chem 48:869
13. Ou S, Lin Z, Duan C, Zhang H, Bai Z (2006) Chem Commun 42:4392
14. Skraup ZH (1880) Ber Dtsch Chem Ges 13:2086
15. Friedlander P (1882) Ber Dtsch Chem Ges 15:2572
16. Combes A (1888) Bull Soc Chim Fr 49:89
17. Doebner O, Miller WV (1881) Ber Dtsch Chem Ges 14:2812
18. Jacob J, Jones WD (2003) J Org Chem 68:3563
19. Huo ZB, Gridnev ID, Yamamoto Y (2010) J Org Chem 75:1266
20. Majumder S, Gipson KR, Odom AL (2009) Org Lett 11:4720
21. Beller M, Thiel OR, Trauthwein H, Hartung CG (2000) Chem Eur J 6:2513
22. Dobbelaar PH, Marzabadi CH (2010) Tetrahedron Lett 51:201
23. Qi CM, Zheng QW, Hua RM (2009) Tetrahedron 65:1316
24. Tanaka SY, Yasuda M, Baba A (2006) J Org Chem 71:800
25. Lin XF, Cui SL, Wang YG (2006) Tetrahedron Lett 47:3127
26. Bian XQ, Liu LH, Geng X, Xie ZY, Li SS, Wang CD (2009) J Chem Res (S) 81
27. Bulgakov RG, Kuleshov SP, Vafin RR, Dzhemilev UM (2009) Russ J Org Chem 45:944
28. Wang B (2005) Synlett 8:1342
29. Zhang M, Jiang HF, Neumann H, Beller M, Dixneuf PH (2009) Angew Chem Int Ed 48:1681
30. Zhang M, Jiang HF, Liu HL, Zhu QH (2007) Org Lett 9:4111
31. Vougioukalakis GC, Grubbs RH (2010) Chem Rev 110:1746
32. Wang XS, Li Q, Zhang MM, Yao CS, Tu SJ (2008) J Heterocycl Chem 45:1027
33. Cho CS, Kim TG, Kim HW (2009) Catal Commun 10:1482