Synthesis of a library of 1,2,3,7-tetrasubstituted indolizines using poly(ethylene glycol) as soluble support

Journal of Heterocyclic Chemistry

Volumn 43, Issue 3, 2006, Pages 781-786

  Yue, Guizhou ^a   Chen, Zuxing ^b   Yang, Guichun ^b  

^a SICHUAN AGRICULTURAL UNIVERSITY   (China)

^b HUBEI UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ALKENE DERIVATIVE; ALKYNE DERIVATIVE; HYDROXIDE; INDOLIZINE DERIVATIVE; MACROGOL; POLYMER; PYRIDINIUM DERIVATIVE;

ARTICLE; CHEMICAL REACTION; CYCLOADDITION; DIPOLE; INFRARED RADIATION; NUCLEAR MAGNETIC RESONANCE; QUANTUM YIELD; SCHOLTZ REACTION; SUBSTITUTION REACTION; SYNTHESIS; THIN LAYER CHROMATOGRAPHY; TSCHITSCHIBABIN REACTION;

EID: 33745002072     PISSN: 0022152X     EISSN: None     Source Type: Journal    
DOI: 10.1002/jhet.5570430340     Document Type: Article

References (44)

1. [1a] M. J. Kurth and R. E. Sammelson. Chem. Rev., 101, 137 (2001);
2. [b] P. J. Wentworth and K. D. Janda. Chem. Commun., 1917 (1999).
3. [2a] T. J. Dickerson, N. N. Reed and K. D. Janda, Chem. Rev., 102, 3325 (2002);
4. [b] X. Zhao, W. A. Metz, F. Sieber and K. D. Janda, Tetrahedron Lett., 39, 8433 (1998);
5. [c] D. J. Gravent, and K. D. Janda, Curr. Opin. Chem. Biol., 1, 107 (1997).
6. S. Chandrasekhar, Ch. Narsihmulu, S. S. Sultana and N. R. Reddy, Org. Lett., 4, 4399 (2002).
7. S. Chandrasekhar, Ch. Narsihmulu and S. S. Sultana, Tetrahedron Lett., 45, 5865 (2004).
8. S. Chandrasekhar, Ch. Narsihmulu, S. S. Sultana and N. R. Reddy. Chem. Commun., 1716 (2003).
9. [6a] S. Chandrasekhar, Ch. Narsihmulu, B. Saritha and S. S. Sultana, Tetrahedron Lett., 45, 5865 (2004);
10. [b] S. Chandrasekhar, N. R. Reddy and S. S. Sultana, Ch. Narsihmulu and K. V. Reddy. Tetrahedron, 62, 338 (2006).
11. [7a] V. V. Namboodiri and R. S. Varma, Green Chem., 3, 146 (2001);
12. [b] J.-H. Li, X.-C. Hu, Y. Liang and Y.-X. Xie, Tetrahedron, 62, 31 (2006);
13. [c] J.-H. Li, W.-J. Liu and Y.-X. Xie, J. Org. Chem., 70, 5409 (2005);
14. [d] L. Liu, Y. Zhang and Y. Wang, J. Org. Chem., 70, 6122, (2005).
15. [8a] N. Panday, T. Granier and A. Vasella, Helv. Chim. Acta, 81, 475 (1998);
16. [b] T. Granier, F. Graiser, L. Hintermann and A. Vasella, Helv. Chim. Acta. 80, 1443 (1997);
17. [c] S. Teklu, L.-L. Gundersen, T. Larsen, K. E. Malterud and F. Rise. Bioorg. Med. Chem., 13, 3127 (2005);
18. [d] S. Teklu, L.-L. Gundersen, F. Rise and M. Tilset, Tetrahedron, 61, 4643 (2005).
19. [9a] Y.-S. Jung and J.-Y. Jaung, Dyes Pigments, 65, 205 (2005);
20. [b] A. I. M. Koraiem, R. M. El-Aal and N. M. S. El-Deer, Dyes Pigments, 68, 235 (2006).
21. P. Sharma, A. Kumar, S. Sharma and N. Rane, Bioorg. Med. Chem. Lett., 15, 937 (2005).
22. S. Zhao, M. G. P. S. Neves, A. C. Tomé, A. M. S. Silva and J. A. S. CavaleIRo, Tetrahedron Lett., 46, 5487 (2005).
23. [12a] N. C. Lungu, A. Dépret, F. Delattre, G. G. Surpateanu, F. Cazier, P. Woisel, P. ShlRaIi and G. Surpateanu, J. Fluorine Chem., 126, 385 (2005);
24. [b] F. Delattre, P. Woisel, G. Surpateanu, F. Cazier and P. Blach, Tetrahedron, 61, 3939 (2005);
25. [c] F. Delattre, P. Woisel, M. Bria and G. Suipateanu, Carbohydrate Res., 340, 1706 (2005).
26. [13a] The recently main methods for indolizines see: ref. [14]; others:
27. [b] K. M. Dawood, Heteroat. Chem., 15, 432 (2004);
28. [c] K. Sarkunam and M. Nallu, J. Heterocyclic Chem., 42, 5 (2005);
29. [d] A. V. Rotaru, I. D. Druta, T. Oeser and T. J. J. Muller, Helv. Chim. Acta, 88, 1798 (2005).
30. L. P. Clarke, J. M. Cole, J. E. Davies, A. French, O. F. Koentjoro, P. R. Raithby and G. P. Shield, New J. Chem., 29, 145 (2005).
31. D. Goff, A. Tetrahedron Lett., 40, 8741 (1999).
32. [16a] Z. Chen, G. Yue, C. Lu and G. Yang, Synlett, 1231 (2004);
33. [b] G. Yue, Y. Wan, S. Song, G. Yang and Z. Chen, Bioorg. Med. Chem. Lett., 15, 453 (2005).
34. The prapradon of TPCD: Y. Hu and H. Hu, Synth. Commun., 22, 1491 (1992) or TPCD was obtained from Aldrich Chemcial. Co..
35. [18a] Y. Hu, X. Wei and H. Hu, In Encyclopecdia of Reagents for Orga. Commun., 27, 1395 (1997);
36. [b] B.Wang, X. Zhang, J. Li, Y. Hu and H. Hu, J. Chem. Soc., Perkin Trans. 1, 1571 (1999);
37. [c] J. Hu, X. Jiang, T. He, J. Zhou, Y. Hu and H. Hu, J. Chem. Soc., Perkin Trans. 1, 1820 (2001);
38. [d] J. Zhou, Y. Hu and H. Hu, Synthesis, 166 (1999);
39. [e] J. Zhou, Y. Hu and H. Hu, J. Chem. Res. (s), 136 (1999).
40. [19a] X. Zhang, W. Cao, J. Li and H. Hu, Synth. Commun., 27, 1395 (1997).
41. [b] B. Wang, X. Zhang, J. Li, Y. Hu and H. Hu, J. Chem. Soc., Perkin Trans. 1, 1571 (1999).
42. [c] J. Hu, X. Jiang, T. He, J. Zhou, Y. Hu and H. Hu, J. Chem. Soc., Perkin Trans. 1, 1820 (2001).
43. [d] J. Zhou, Y. Hu and H. Hu, Synthesis, 166 (1999).
44. [e] J. Zhou, Y. Hu and H. Hu, J. Chem. Res.(s), 136 (1999).