Synthesis of calix[4]arene diazacrown containing m-xylylene phenol subunit

Organic Preparations and Procedures International

Volumn 34, Issue 5, 2002, Pages 552-557

  Wan, Xiao Bing ^a   Lu, Guo Yuan ^a   Bo, Zhu ^a   Jin, Chum Ming ^a   Liu, Fang ^a  

^a NANJING UNIVERSITY   (China)

Author keywords

[No Author keywords available]

Indexed keywords

CALIX[4]ARENES;

PHENOLS;

ACETONITRILE DERIVATIVE; ALCOHOL; ALDEHYDE DERIVATIVE; CALIXARENE; CALIXARENE DIAZACROWN; DIAMINE; PHENOL DERIVATIVE; SCHIFF BASE; UNCLASSIFIED DRUG;

ANALYTIC METHOD; ARTICLE; CHEMICAL COMPOSITION; MOLECULAR WEIGHT; POLYMERIZATION; PROTON NUCLEAR MAGNETIC RESONANCE; SYNTHESIS;

EID: 85023516765     PISSN: 00304948     EISSN: 19455453     Source Type: Journal    
DOI: 10.1080/00304940209355781     Document Type: Article

References (24)

1. A. Ikeda and S. Shinkai, Chem. Rev., 97,1713 (1997).
2. V. Böhmer, Angew. Chem. Int. Ed. Engl., 34,713 (1995).
3. A. F. D. de Namor, R. M. Cleverley and M. L. Zapata-Ormachea, Chem. Rev., 98, 2495 (1998).
4. Y. Y. Chen, F. F. Yang and S. L. Gong, Tetrahedron Lett., 41,4815 (2000).
5. J. S. Li, Y. Y. Chen and X. R. Lu, Eur. J. Org. Chem., 3,485 (2000).
6. G. Ferguson, J. F. Gallagher, A. J. Lough, A. Notti, S. Pappalardo and M. F. Parisi, J. Org. Chem., 64,5876 (1999).
7. G. Ferguson, A. J. Lough, A. Notti, S. Pappalardo, M. F. Parisi and A. Petringa, J. Org. Chem., 63,9703 (1998).
8. J. S. Kim, H. H. Suh, J. K. Kim and M. H. Cho, J. Chem. Soc. Perkin. Trans 1., 2307 (1998).
9. M. Blanda, D. B. Farmer, J. S. Brodbelt and B. J. Goolsby, J. Am. Chem. Soc., 122,1486 (2000).
10. M. Takeshita and S. Shinkai, Bull. Chem. Soc. Jpn, 68,1088 (1995).
11. J. S. Kim, A. Ohki, R. Ueki, T. Ishizuka, T. Shimotashiro and S. Maeda, Talanta, 48,705 (1999).
12. H. Yamamoto and S. Shinkai, Chemistry Lett., 1115 (1994).
13. K. E. Krakowiak, J. S. Bradshaw and D. J. Zamecka-Krakowiak, Chem. Rev., 89,929 (1989).
14. F. C. J. M. van Veggel, S. Harkema, M. Bos, W. Verboom, C. J. van Staveren, G. J. Gerritsma and D. N. Reinhoudt, Inorg. Chem., 28,1133 (1989).
15. T. Nagata, Y. Ikawa and K. Maruyama, Chem.Commun., 471 (1994).
16. V. Böhmer, G. Ferguson, J. F. Gallagher, A. J. Lough, M. A. Mckervey, E. Madigan, M. B. Moran, J. Phillips and G. Williams, J. Chem Soc. Perkin Trans 7,1521 (1993).
17. I. Bitter, A. Grun, G. Toth, B. Baldzs and L. Toke, Tetrahedron, 53,9799 (1997).
18. I. Bitter, A. Grun, G. Toth, B. Balazs, G. Horvath and L. Toke, Tetrahedron, 54,3857 (1998).
19. A. Ikeda, T. Tsudera and S. Shinkai, J. Org. Chem., 62,3568 (1997).
20. J. S. Kim, I. Y. Yu, I. H. Suh, D. Y. Ra and J. W. Kim, Synth. Commun., 28,2937 (1998).
21. F. Szemes, D. Hesek, Z. Chen, S. W. Dent, M. G. B. Drew, A. J. Goulden, A. R. Graydon, A. Grieve, R. J. Mortimer, T. Wear, J. S. Weightman and P. D. Beer, Inorg. Chem., 35,5868 (1996).
22. H. S. Yuan and Z. T. Huang, Chin. Chem. Lett., 10,539 (1999); Chem. Abst., 132,166225.
23. W. C. Zhang and Z. T. Huang, Synthesis, 1073 (1997).
24. S. Taniguch, Bull. Chem. Soc. Jpn, 57,2683 (1984).